Remote Slovakia
Precision for Medicine is growing and we are looking for an exceptional Principal Database Programmer to join our European team. This is a full-time permanent position that can be covered fully remotely from our European locations. Job Summary The Principal Database Programmer is responsible for managing all programming aspects of the database (development testing implementation maintenance and support of clinical databases and applications) from study start to post database lock for assigned projects. This position works closely with other departments and interfaces directly with the internal team and external teams (e.g. Data Management Project Management EDC vendors clients and third-party vendors) to provide status updates and gather requirements ensure database is developed maintained managed and that it complies with regulatory guidelines. Responsible for leading the operational study team and programming team members on assigned studies and study programs. Responsible for operational and technical training to end users and junior staff. Responsible for providing planning estimates for project scope schedule/timelines forecasting and resource requirements. Main Duties & Responsibilities Maintains responsibility of assigned projects. Ensures on-time delivery communicates the status of projects to internal teams and study Maintains awareness of the key elements of the contract and scope of work for assigned project(s) and communicates status updates to the Project team as necessary. Performs project forecasting of hours and identification of resource requirements and manages project budgets including identification of out-of-scope work and post production changes Provides input and guidance to the design of clinical databases to the client and internal teams Builds and supports clinical databases Develops tests and validates programs and clinical database to support client-related projects and third-party applications. Provides system administration and advanced technical support services for internally developed applications and clinical databases client-related projects and third-party applications Troubleshoots and resolves software and clinical database problems Develops and maintains study-specific validation documents Provides support to data management for client-related projects from CRF design to post database close and archival May design develop and validate the Company’s internal applications client-related projects and third-party applications. Participate in software vendor selection Participate in conducting EDC demonstrations and trainings Participate in the development and maintenance of Standard Operating Procedures (SOPs) and corresponding process documentation related to data management and database management activities Supports with onboarding of new hires Provide leadership for cross-functional and organization-wide initiatives where applicable Trains and ensures that all data management project team members have been sufficiently trained Communicate with study sponsors vendors and project teams as needed regarding data database or other relevant project issues Present software demonstrations/trainings department/company training sessions present at project meetings Performs all duties in accordance with SOPs government regulations guidelines and industry standards. May require some travel Perform other duties as assigned Requirements Minimum Education & Experience Minimum 8 years’ experience Bachelors and/or a combination of related experience Strong experience in Oncology experience with Autoimmune diseases would be a strong adventage Strong experience with Rave and Veeva Proficiency in Microsoft Office Word Excel PowerPoint Outlook. Experience in Object Oriented Programming (C C++ VBS etc.…) Understanding of CDISC standards (CDASH SDTM ADaM etc.) Proficiency in more than one CDMS system to include building forms edit checks and complex rule development. Awareness of CRF standards and input to maintenance of standards library. Ability to troubleshoot and support peers with technical issues and build solutions.Broad knowledge of drug device and/or biologic development and effective data management practices Able to handle a variety of clinical research tasks. Excellent organizational and communication skills Professional use of the English language both written and oral. Experience in clinical database management system development. Experience in a clinical scientific or healthcare discipline. Strong leadership and interpersonal skills Preferred Education & Experience (optional) Experience in a clinical scientific or healthcare discipline and multiple therapeutic area experience Experience in utilizing various Database Programming systems Ability to work independently manage time and create plans to achieve project revenue and business goals Ability to work effectively with minimal direction must be a self-motivated and self-directed individual who enjoys a challenging and dynamic work environment Team player willing to collaborate and share knowledge Highly organized Effective communication interpersonal and negotiation skills Excellent organization and prioritization skills Exceptional customer service orientation and proven track record of successful client relationship management LI-Remote LI-TB1 Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants please also refer to our CA Privacy Notice Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race color age religion sex sexual orientation gender identity national origin disability veteran status or other characteristics protected by law. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying you may contact Precision Medicine Group at myHR@precisionmedicinegrp.com Recruitment Fraud Warning Please be aware that fraudulent individuals and websites may impersonate Precision Medicine Group or its affiliates and attempt to obtain personal financial or banking information through fake job postings or employment offers. Precision Medicine Group will never request payment banking details or other sensitive financial information as part of the recruitment process. If you believe you have been targeted by a recruitment scam we encourage you to report the incident to your local law enforcement authorities consumer protection agency or relevant cybercrime reporting organization in your country. Please also notify us at myHR@precisionmedicinegrp.com so we can investigate and take appropriate action.
Remote Czechia / Remote Slovakia / Remote Italy
As a Data Analyst (Slovak) you will support Lightcast's global data initiatives by analyzing and improving multilingual data quality. Working closely with Linguistics and Engineering teams you will help develop parsers evaluate text classifiers and translate key taxonomies to ensure we deliver high-quality data to customers across global markets. This is a full-time (40 hours per week) independent contractor position for up to 6 months and requires candidates to provide their own laptop and reliable internet access. ➡ Major Responsibilities ➡ Analyze and improve the data quality of multilingual text classifiers Partner with Linguistics and Engineering teams to develop parsers across multiple languages Translate taxonomies including Skills Titles and Occupations Analyze and clean data using Excel and other data analysis tools Apply language data and text analysis expertise to support high-quality global data Education & Experience ➡ Proficiency in reading and writing Slovak required including an understanding of language syntax and structural analysis Reliable laptop and internet access required Multilingual candidates strongly preferred particularly those proficient in Czech Bachelor's degree in Linguistics Data Analytics Natural Language Processing (NLP) or a related field preferred Experience with Microsoft Excel including VLOOKUPs data cleanup and functions Knowledge of query languages such as SQL Advanced knowledge of rule writing using regular expressions (RegEx) Knowledge of text analysis or machine learning principles Experience with data analysis using tools such as Excel Ability to perform repetitive detail-oriented work with accuracy and consistency Ability to follow complex instructions navigate ambiguity and work independently Strong sense of urgency organization and time management ➡ Lightcast is a global leader in labor market insights with headquarters in Moscow ID (US) and offices in the United Kingdom Europe and India. We work with partners across six continents to help drive economic prosperity and mobility by providing the insights needed to build and develop our people our institutions and companies and our communities. Lightcast is proud to be an equal opportunity workplace and does not discriminate on the basis of federally protected statuses. Lightcast has always been and always will be committed to diversity of thought and unique perspectives. We seek dynamic professionals from all backgrounds to join our teams and we encourage our employees to bring their authentic original and best selves to work.
Remote Slovakia
Are you an experienced Clinical Project Manager in the field of clinical trials who’s engaged in addressing the challenges facing the research and development of novel compounds. Are you passionate about impacting the health and lives of patients around the world? Do you take a consultative approach to trial management proving to be a valuable partner in trial operational delivery? As a Project Manager within our FSP Group you will provide operational leadership and oversight for assigned FSP (Functional Service Provider) projects to ensure that contracted deliverables are accomplished. You may manage regional trials (moderate complexity) and/or support complex global trials. The essential functions below will describe the FSP PM acting in a primary / lead FSP PM role on a project. When in a supportive role on a global study the essential functions will be delegated by the Global Lead. Provide program-level leadership and operational oversight for assigned FSP collaboration activities to support achievement of contracted deliverables. Serve as the primary operational point of contact for the client at the FSP project level including coordination of routine project communication issue escalation resolution tracking and follow-up on agreed actions. Coordinate cross-functional activities across internal stakeholders FSP team members functional line managers study teams and client stakeholders to ensure aligned execution within contracted deliverables. Support development maintenance and implementation of FSP program-specific processes procedures trackers working guidelines communication pathways and governance materials. Monitor project-level risks issues resource constraints quality trends and operational gaps escalate appropriately and support development of mitigation or corrective action plans. Support financial oversight of assigned FSP project activities including review of scope assumptions resource utilization budget pass-through expenses forecasting inputs and financial risks in collaboration with Finance and FSP leadership. Lead organize and facilitate internal and client-facing operational meetings as necessary including preparation of agendas and minutes follow-up of actions presentation of program updates and escalation of key decisions or risks. Contribute to onboarding training mentoring and coaching of FSP team members as needed including support for role expectations client-specific requirements operational processes and escalation pathways. Education and Experience Required Bachelor’s degree or equivalent combination of education and experience preferably in life sciences healthcare clinical research or a related discipline Minimum of 3-5 years of clinical research experience including experience in clinical operations project/program oversight FSP delivery or functional service management or proven competencies for this position and a minimum of 2 years leading a project. Experience managing regional trials (moderate complexity) and/or supportive role in managing complex global trails including within the area of Auto Immune Disease areas Strong working knowledge of ICH-GCP applicable regulatory requirements clinical trial conduct and clinical research operational processes. Experience supporting quality oversight metrics review issue escalation risk management or inspection/audit readiness activities. Experience working with clinical trial systems such as EDC eTMF CTMS reporting dashboards trackers or other operational management tools. Proficiency in Microsoft Office applications including Word Excel PowerPoint Outlook and Teams. Other Skills and Competencies Required Strong understanding of clinical research operations FSP delivery models and client-service expectations within a CRO or sponsor-facing environment. Excellent communication and interpersonal skill to effectively interface with clients and internal stakeholders (i.e. functional line managers study teams Finance Talent Acquisition and senior leadership). Strong planning organizational and problem-solving skills with the ability to manage competing priorities and drive follow-up in a fast-paced environment. Ability to coordinate cross-functional deliverables and promote alignment across teams functions countries and client stakeholders. Strong quality mindset with the ability to monitor metrics identify risks or trends escalate issues appropriately and support practical mitigation or corrective actions. Sound financial and commercial awareness including ability to understand scope resource assumptions budget impact and utilization. Effective escalation management skills including judgment to determine when issues require client internal leadership Finance HR or operational escalation Strong written and verbal communication skills in English including ability to prepare clear program updates meeting materials client communications and action-oriented follow-up. Elevated level of professionalism accountability cultural awareness attention to detail and ability to work independently while maintaining strong collaboration with stakeholders. We are a people focussed CRO with a supportive and collaborative environment which promotes work life balance and encourages team development. We invite you to learn more about our growing organization serving our clients that are researching ground-breaking cancer therapies. We strive to ensure employees feel appreciated for the contributions they make every single day. Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants please also refer to our CA Privacy Notice Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race color age religion sex sexual orientation gender identity national origin disability veteran status or other characteristics protected by law. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying you may contact Precision Medicine Group at myHR@precisionmedicinegrp.com Recruitment Fraud Warning Please be aware that fraudulent individuals and websites may impersonate Precision Medicine Group or its affiliates and attempt to obtain personal financial or banking information through fake job postings or employment offers. Precision Medicine Group will never request payment banking details or other sensitive financial information as part of the recruitment process. If you believe you have been targeted by a recruitment scam we encourage you to report the incident to your local law enforcement authorities consumer protection agency or relevant cybercrime reporting organization in your country. Please also notify us at myHR@precisionmedicinegrp.com so we can investigate and take appropriate action.
Remote Slovakia
Job Summary and Purpose The Senior Operations Specialist leverages expertise and knowledge to plan and manage initiatives and activities designed to improve the quality efficiency and effectiveness of the delivery of studies to Sponsors. The Sr Operations Specialist develops and implements processes change management plans standards or operational plans with the goal of operational excellence across the business collaborating across a group of diverse stakeholders. They will support a wide range of activities within the Business & Operational Excellence group. Specific tasks depend on the functional area including Process improvement support of training content and/or development and deployment of change management initiatives. This role executes functional priorities with minimal oversight. Main Duties & Responsibilities Support the vision of and commitment to continuous improvement in operational excellence across all activities. Lead the evaluation of business processes and workflows to identify opportunities for improvement or automation under direction of a supervisor. Participate with stakeholders in root-cause problem-solving techniques to identify core process challenges. Support the development of recommendations for process improvement leveraging subject matter experts for critical input. Partner with cross functional leadership to prioritize improvement opportunities and support strategic initiatives. Partner on the design and implementation of new business processes with organizational context and priorities in mind. Lead change management initiatives and support business through a communication framework assessment of impact on roles and deploy a variety of tactics to support change management effort to ensure adoption and sustainability of process changes. Lead internal communication to effectively update stakeholders on progress performance key issues and blockers that may impact business attainment or critical program and project completion Identify operational risks and lead implementation of mitigation plans. Ensure or lead the documentation of business process. Work with leadership to establish key performance metrics and dashboards for monitoring operational performance. Provide insight into training and guidance to teams on new processes and how to identify improvement opportunities building awareness on continual improvement initiatives Support standardized best practices and processes across the organization to ensure consistency and sustainability. Monitor measure and analyze the effectiveness of new initiatives and processes making adjustments as needed. Monitor adoption of process system and organizational changes to ensure long term and sustained adoption. Prepare and maintain tools and templates to support execution Schedule meetings take notes and track actions Travel as needed Education and Experience Minimum Bachelor's degree or equivalent experience 5-7 years in change management operations support and process improvement experience Experience in CRO/pharmaceutical/biotechnology drug development or demonstrated competency in the key areas of the role Strong drug development experience with understanding of other functions relevant to the position. Knowledge Skills and Competencies Proficiency in Microsoft Office (Outlook Word Excel PowerPoint Teams) Strong written and verbal English communication skills Knowledge of ICH-GCP and regulatory guidance Strong interpersonal and training skills Self-motivated and detail-oriented Ability to work independently and in teams Strong professionalism sense of ownership and pride in quality of outputs Understanding of change management models (ie ADKAR) and use of change radars Flexible attitude with respect to work assignments and ability to thrive in a fast-paced dynamic environment Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants please also refer to our CA Privacy Notice Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race color age religion sex sexual orientation gender identity national origin disability veteran status or other characteristics protected by law. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying you may contact Precision Medicine Group at myHR@precisionmedicinegrp.com Recruitment Fraud Warning Please be aware that fraudulent individuals and websites may impersonate Precision Medicine Group or its affiliates and attempt to obtain personal financial or banking information through fake job postings or employment offers. Precision Medicine Group will never request payment banking details or other sensitive financial information as part of the recruitment process. If you believe you have been targeted by a recruitment scam we encourage you to report the incident to your local law enforcement authorities consumer protection agency or relevant cybercrime reporting organization in your country. Please also notify us at myHR@precisionmedicinegrp.com so we can investigate and take appropriate action.
Remote Slovakia
Due to our continued growth Precision for Medicine is looking for a Senior Feasibility Associate/Feasibility Manager to join our European team. This position can be covered fully remotely in UK Spain Hungary Poland Romania Serbia or Slovakia. Position Summary The Senior Feasibility Associate/Feasibility Manager is a member of the expert team within Feasibility Department of Precision for Medicine. As part of this team this role has responsibility to support the delivery of pre-award post-award rescue and stand-alone-feasibility projects. The Senior Feasibility Associate/Feasibility Manager supports pre-award feasibility projects and support business development and operational strategy teams by conducting feasibility analysis. The Senior Feasibility Associate/Feasibility Manager supports stand-alone feasibility projects and site identification and is providing feasibility support for newly awarded and/or ongoing projects. In addition Senior Feasibility Associate/Feasibility Manager may participate in specific projects that enables Precision for Medicine to stay at the forefront of innovation and maintain their competitive edge as a scientifically driven engaged partner for our biotech and pharma clients. Essential functions of the job include but are not limited to Support pre-award feasibility projects Provide pre-award feasibility analysis and input for pre-award RFPs including competitive analysis historical recruitment analysis standards of care drug analysis epidemiology analysis site and country analysis. Review clinical protocols study assumptions client information and study plans for US and global trials. Present and explain feasibility analysis to BD/Clients including the process recommendations and rationale. Interface with colleagues consultants and partners and collaborate with internal and external sources to gather and share feasibility information. Undertake feasibility site outreach for pre award opportunities. Participate and/or contribute to BDM and client calls. Provide support to post-award feasibility projects Undertake post-award rescue and standalone feasibility deliverables in alignment with study and client requirements. Where appropriate engage with patient advocacy groups and site networks to support study feasibility recruitment and successful delivery. Support the analysis of the collected site data to provide accurate site identification enrollment modeling and study strategy (ies) Minimum required Bachelor’s degree in a life sciences discipline A minimum of 5 years of related experience Combination of qualifications and equivalent relevant experience may be accepted as an alternative. Other Required Relevant experience in the required activities for the role including feasibility analysis site identification. Ability to communicate both verbally and in writing at the English proficiently (Professional level) Preferred Postgraduate degree preferred. Skills Strong management and organizational skills Excellent oral and written communication skills in English Strong rationale and analytical thinking Strong IT platform and data analysis skills Strong presentation abilities Advanced computer skills specifically with MS Word Excel PowerPoint and with web/data-based platforms Competencies Strong sense of ownership and pride in quality of outputs Good to strong attention to detail with ability to see the big picture Team player Willingness to work in a matrix environment work independently and as part of a dynamic team. Demonstrates knowledge of ICH-GCP Precision for Medicine is not your typical CRO. At Precision for Medicine we have brought together new technologies expertise and operational scale to help the life sciences improve the speed cost and success rate of bringing life-changing therapies to patients. What sets us apart is the way we integrate clinical trial execution with deep scientific knowledge laboratory expertise and advanced data sciences. We have a strong focus on Oncology and Rare Disease. #LI-TB1 #LI-Remote Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants please also refer to our CA Privacy Notice Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race color age religion sex sexual orientation gender identity national origin disability veteran status or other characteristics protected by law. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying you may contact Precision Medicine Group at myHR@precisionmedicinegrp.com Recruitment Fraud Warning Please be aware that fraudulent individuals and websites may impersonate Precision Medicine Group or its affiliates and attempt to obtain personal financial or banking information through fake job postings or employment offers. Precision Medicine Group will never request payment banking details or other sensitive financial information as part of the recruitment process. If you believe you have been targeted by a recruitment scam we encourage you to report the incident to your local law enforcement authorities consumer protection agency or relevant cybercrime reporting organization in your country. Please also notify us at myHR@precisionmedicinegrp.com so we can investigate and take appropriate action.
Remote Slovakia
Precision for Medicine is a Clinical Research Organization. Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs industry-leading operational and medical experts advanced biomarker and data analytics solutions and an unequivocal real passion for rare diseases and oncology in addition to working across other therapeutic areas. Due to continued growth we are currently seeking a Project Support Specialist The Project Support Specialist will serve as a member of the project team providing cross-functional support with the goal of contributing toward efficient management of the studies to which they are assigned. This position can be offered fully home based in the following locations - Poland Serbia Slovakia Hungary or Romania. Essential functions of the job include but are not limited to Creates and maintains the project timeline in MS Project or similar system. Ensures updates are captured and documented. Ensures the distribution of updates to study team members. Schedules internal and external meetings assists with preparing and circulating agendas takes meeting minutes circulates meeting minutes and files meeting agendas and minutes in the Trial Master File. Performs an array of activities in the Clinical Trial Management System (CTMS) including maintaining study milestone dates updating study contact lists maintaining enrolment projections as needed and submitting helpdesk tickets and ensuring remediation is completed. Prepares assigns and documents study-specific training in appropriate systems manages and oversees the maintenance of training records. Identifies gaps in training and engages appropriate team members or escalates as needed. Establishes a study-level Share Point site or similar shared working space and ensures appropriate access to study team sponsors and others as appropriate. Creates project-specific email boxes and maintains appropriate access to study team members. Manages user access to study systems by submitting user requests to the Help Desk or similar by reviewing team member access on a define periodic basis and document access review. Orders study supplies and addresses queries on study supplies. Orders initial study binders. Collects collates and prepares study binders and ensures shipping to the proper locations through printing vendor. Maintains various study trackers as needed and directed by the Project Manager Clinical Trial Manager or other project leader. Sends communications to study sites investigators and others as directed by the Project Manager Clinical Trial Manager or other Project Leadership including SUSARs email blasts newsletters and other information that may be required. May support the distribution and tracking of IND Safety Reports/SUSARS/CIOMS according to the procedures defined by the study team in the project plan as applicable may be under Safety staff guidance. May support the translation process of site level documents as applicable per local and regional standards. May act as point of contact for project-related requests for team members Sponsors and third party vendors. Supports the preparation distribution and the reconciliation of study material during applicable phases of the study (Operations Manual ISF patient cards etc.) as applicable. May support team leaders with the production of various study reports and updates (e.g. country/site initiation activation recruitment). Performs other duties as assigned by the Project Manager Clinical Trial Manager or other Project Leadership. Qualifications Minimum Required 4-year college degree or equivalent experience ideally in a business scientific or healthcare discipline Minimum of 2 years of relevant experience as a Clinical Trial Assistant Clinical Support Specialist or similar position. Other Required Fluency in the Microsoft Office package of programs (Outlook Word Excel and PowerPoint). Customer service demeanour demonstrate flexibility teamwork and a keen attention to detail. Ability to communicate both verbally and in writing at the English proficiently (Professional level). Competencies Working knowledge of ICH-GCP Precision SOPs and regulatory guidance. Demonstrates solid interpersonal skills. Exhibits strong self-motivation is detail-oriented and able to work and plan independently as well as in a team environment. Strong written and verbal communication skills Commitment to performing professionally consistent with Precision Principles. #LI-OS1 #LI-Remote Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumours on a molecular level using biomarkers to link specific mutations to specific treatments. We combine deep science with deep data from advanced technological platforms then layer on specialized expertise in the design and execution of targeted adaptive clinical trials. Ultimately we deliver robust insights that inform real-time decisions—and optimize the oncology development pathway. Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants please also refer to our CA Privacy Notice Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race color age religion sex sexual orientation gender identity national origin disability veteran status or other characteristics protected by law. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying you may contact Precision Medicine Group at myHR@precisionmedicinegrp.com Recruitment Fraud Warning Please be aware that fraudulent individuals and websites may impersonate Precision Medicine Group or its affiliates and attempt to obtain personal financial or banking information through fake job postings or employment offers. Precision Medicine Group will never request payment banking details or other sensitive financial information as part of the recruitment process. If you believe you have been targeted by a recruitment scam we encourage you to report the incident to your local law enforcement authorities consumer protection agency or relevant cybercrime reporting organization in your country. Please also notify us at myHR@precisionmedicinegrp.com so we can investigate and take appropriate action.
Remote Slovakia
We are hiring a Manager Learning and Development based in Hungary Poland Romania Serbia or Slovakia to join our team. The Manager Learning & Development is responsible for supporting training strategy identifying developing and delivering training solutions that support global Precision for Medicine functions. This role partners with subject matter experts to design effective learning programs across translational sciences (labs and logistics) clinical operations project management GCP data management and regulatory/compliance areas in support of functional and GCP requirements. The Manager serves as the primary intake point for training requests coordinates new hire onboarding and supports refinement of learning technologies and platforms. Clear communication and collaboration with stakeholders and L&D leadership are essential to success in this role. Main Duties & Responsibilities Partner with functional SMEs to assess training needs design and develop appropriate content and deliver effective learning solutions. Lead coordination and delivery of new hire role specific onboarding for Precision for Medicine including scheduling and tracking as applicable. Design and deliver instructor‑led virtual and e‑learning training programs aligned with adult learning principles. Serve as first‑line triage for training requests and provide guidance on existing tools templates and materials. Manage and support learning platforms and systems used by the L&D function. Maintain accurate training documentation records and reporting in accordance with regulatory expectations. Collaborate with functional leadership to establish and maintain role‑based curricula by function including documented annual reviews of curricula and training hour requirements with updates completed as regulations organizational needs or role expectations evolve. Education and Experience Graduate postgraduate 4-year college degree or equivalent experience in a scientific or healthcare discipline. Experience working for a Clinical Research Organisation (CRO) with 4-6 yrs of learning and development experience supporting delivery teams. Proficiency with learning development platforms. Proficiency with Microsoft Office. Excellent verbal communication skills be able to communicate effectively in the English language. Strong writing and recordkeeping abilities. Ability to plan and manage multiple complex projects. Demonstrated ability to develop positive working relationships with individual and teams internally and externally. Core understanding of medical terminology and clinical trial activities in relation to execution of a clinical development plan. Strong knowledge of ICH/GCP relating to clinical trial management. Precision for Medicine is the first global precision medicine clinical research services organization purpose-built to improve the clinical research and development process for new therapeutics. Our novel approach integrates clinical operations excellence with laboratory expertise and advanced data sciences to inform every step. We apply our expertise to trials at all stages—from early development through approval—with embedded experience in oncology and rare disease. #LI-NC1 #LI-Remote Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants please also refer to our CA Privacy Notice Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race color age religion sex sexual orientation gender identity national origin disability veteran status or other characteristics protected by law. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying you may contact Precision Medicine Group at myHR@precisionmedicinegrp.com Recruitment Fraud Warning Please be aware that fraudulent individuals and websites may impersonate Precision Medicine Group or its affiliates and attempt to obtain personal financial or banking information through fake job postings or employment offers. Precision Medicine Group will never request payment banking details or other sensitive financial information as part of the recruitment process. If you believe you have been targeted by a recruitment scam we encourage you to report the incident to your local law enforcement authorities consumer protection agency or relevant cybercrime reporting organization in your country. Please also notify us at myHR@precisionmedicinegrp.com so we can investigate and take appropriate action.
Remote Slovakia
Precision for Medicine is hiring a Project Manager Central Laboratory Services to work remotely from Poland Serbia Romania Hungary Slovakia or the UK. Position Summary This role will lead new and existing CRO laboratory projects across a range of disciplines all with the focus on accelerating the development and adoption of novel therapeutics. This includes assay development and clinical testing biorepository/sample management and logistics and kitting for client studies spanning the globe. This is a key role which is client-facing ensuring project plans are translated into action and results requiring internal cross-functional leadership. Leads and manages all aspects of designated protocols and is accountable for overall project performance and client satisfaction by meeting their needs and expectations throughout the lifecycle of assigned projects. Provides internal consulting on project management issues and identifies opportunities for process and efficiency improvement. Serves as the cross-functional lead for assigned projects and monitors operational delivery progress against contracted timelines and budget. Prepares and maintains process documents and mentors junior Project Managers. Essential Information · Leads projects from conception through close-out ensuring detailed planning and execution risk management communication and stakeholder management scope and cost control · Works on problems of moderate scope where analysis of situations and/or data requires a review of a variety of factors · Navigates ambiguity and has a system and process solution mindset to support growth and continuous improvement · Developing professional expertise applies company policies and procedures to resolve a variety of issues · Contacts are both internal to the company and external with client/vendor on routine matters · Builds productive internal/external working relationships · Normally receives general instructions on routine work detailed instructions on new projects or assignments · Exercises judgment within defined procedures and practices to determine appropriate action Essential functions of the job include but are not limited to · Excellent listening and communication skills has an uncanny ability to make internal colleagues and clients feel understood · Create and manage project timelines budgets and revenue goals forecasting resource plans while comparing to contracted project scope(s) fully exploring new ideas that optimize quality and efficiency · Maintain detailed daily coordination and supervision of scheduled activities delegating responsibilities to carry out contracted work activities as appropriate · As the face of the company and key partner to clients and collaborators effectively lead implementation of new and ongoing studies · Coordinate the development and implementation of new projects · Create track and report on project timelines · Communicate with clients and collaborators with regards to data management inventory control shipping procedures etc. for all assigned areas · Respond in a timely manner to all events · Coordinate data gathering · Prepare and present project information at internal and external meetings prepare reports and correspondences to clients collaborators and vendors · Meet all revenue objectives assigned to projects project expenses and client billing. Evaluate contract/project budgets monthly and report unexpected variances to department director · Create/track/report relevant metrics for business and project measurement · Assist senior staff as required · Identify out of scope project work escalate findings and action plans to appropriate parties · Manage all tasks in an efficient and timely manner ensuring client expectations are met and are delighted · Review update and evolve all documentation associated with project(s) to approvable status · Assess and mitigate technical project and business risks · Ensure that work product complies with design and performance standards regulatory environment and client expectations. Enforce standards applicable to each step in project execution · Identify resolve and assist in resolution of operational issues · Monitors assignments and adjusts priorities and work schedule to meet deadlines and provide high quality deliverables. Completes additional tasks needed in support of project client and departmental objectives · Complete other responsibilities as assigned Qualifications Minimum Required Bachelor's degree in a life science or related field (e.g. engineering) Must have experience working as a Project Manager for Central Laboratories either for a CRO Pharmaceutical or Biotech company. Excellent listening and communication skills has an uncanny ability to make internal colleagues and clients feel understood Other Required Excellent computer skills and experience with MS Office/MS 365 applications Excellent presentation interpersonal organizational and multi-tasking skills exceptional emotional intelligence Strong understanding of project management and data analysis Strong critical thinking analytical and problem-solving skills Exceptional research and reporting skills Exceptional use of judgement and discretion Able to read write and fluently speak and comprehend the English language Must be able to travel both domestically and internationally including overnight stays (~10-25%) Extended work hours may be necessary in order to meet business demands #LI-NC1 #LI-Remote Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants please also refer to our CA Privacy Notice Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race color age religion sex sexual orientation gender identity national origin disability veteran status or other characteristics protected by law. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying you may contact Precision Medicine Group at myHR@precisionmedicinegrp.com Recruitment Fraud Warning Please be aware that fraudulent individuals and websites may impersonate Precision Medicine Group or its affiliates and attempt to obtain personal financial or banking information through fake job postings or employment offers. Precision Medicine Group will never request payment banking details or other sensitive financial information as part of the recruitment process. If you believe you have been targeted by a recruitment scam we encourage you to report the incident to your local law enforcement authorities consumer protection agency or relevant cybercrime reporting organization in your country. Please also notify us at myHR@precisionmedicinegrp.com so we can investigate and take appropriate action.
Remote Slovakia
Are you an experienced full service Project Manager in the field of clinical trials who’s engaged in addressing the challenges facing the research and development of novel compounds in Oncology. Are you passionate about impacting the health and lives of patients around the world? Do you take a consultative approach to trial management proving to be a valuable partner in trial operational delivery? Precision for Medicine are looking to hire a Clinical Project Manager / Senior Clinical Project Manager with experience in Oncology who have managed full service clinical trials within a CRO setting to join our global team. In this pivotal role you will have full service oversight for clinical projects across global/regional (ph I-IV) trials within Oncology. Accountable for clinical project delivery oversight of all functional departments and ensuring agreed timelines scope cost and quality. Involved in all study stages including proposal strategy development costing and bid defence and seeing studies through the full cycle to completion managing the client relationship project team and budget and timelines throughout. You will work in a cross-functional team with both internal and external stakeholders driving quality and coordinating the study team. We offer an amazing high-energy dedicated collaborative team members who enjoy a challenge thrive in the details and flourish in dynamic environments. If you are no stranger to taking charge and seek positive teamwork to deliver extraordinary work we have an opportunity for you. How we will keep you busy and support your growth You will independently lead clinical projects in accordance with the study budget and scope of work. You will use your strong interpersonal and organizational skills to set and achieve objectives in the execution of the projects both contracted objectives and financial objectives. You may be called upon to run international trials as well. Serve as the primary point-of-contact liaison with the client to provide excellent customer service including participation in proposal activities and client presentations Liaise with Project Team and senior management of both Precision and sponsors including C level Handle and lead all aspects of a clinical research trial or trials Total project management for all functional areas including data management safety clinical medical monitoring and biostatistics etc. Prepare project status updates for clients and management identifying key deliverables and performance metrics of success and escalation. Serve as an active member of the Project Team with the goal to contribute towards efficient management and execution of trials Prepare and reviews protocols and other study documentation such as project plans inform consents site contracts and budgets Requirements Degree or similar related life science qualification or equivalent combination of education and experience. Previous experience in a full service/global Project Management role working in the CRO industry is essential. Extensive experience working within Clinical Operations position within a CRO and at least 4 years full service Project Management experience in a clinical trial setting working for a Clinical Research Organisation. Experience managing studies within Oncology Working understanding of GCP/ICH guidelines and the clinical development process Ability to drive and availability for domestic and international travel including overnight stays Be able to communicate effectively in the English language both written and spoken Strong presentation skills Proven computer skills (MS Office MS Project PowerPoint) and software experience (CTMS eTMF EDC IXRS) Proven ability to develop positive working relationships with individual and teams internally and externally Demonstrated core understanding of medical terminology and clinical trial activities as it relates to the execution of a clinical development plan Precision for Medicine's uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs industry-leading operational and medical authorities advanced biomarker and data analytics solutions and an unequivocal real passion for rare diseases and oncology. We are a people focussed CRO with a supportive and collaborative environment which promotes work life balance and encourages team development. We invite you to learn more about our growing organization serving our clients that are researching ground-breaking cancer therapies. We strive to ensure employees feel appreciated for the contributions they make every single day. Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants please also refer to our CA Privacy Notice Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race color age religion sex sexual orientation gender identity national origin disability veteran status or other characteristics protected by law. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying you may contact Precision Medicine Group at myHR@precisionmedicinegrp.com Recruitment Fraud Warning Please be aware that fraudulent individuals and websites may impersonate Precision Medicine Group or its affiliates and attempt to obtain personal financial or banking information through fake job postings or employment offers. Precision Medicine Group will never request payment banking details or other sensitive financial information as part of the recruitment process. If you believe you have been targeted by a recruitment scam we encourage you to report the incident to your local law enforcement authorities consumer protection agency or relevant cybercrime reporting organization in your country. Please also notify us at myHR@precisionmedicinegrp.com so we can investigate and take appropriate action.
Remote Slovakia
Precision for Medicine is looking for a Site Contracts Manager to join our European Team. The position can be covered fully remotely from the Poland Slovakia Spain Serbia Romania or Hungary. Position Summary Review draft negotiate and track a variety of legal agreements including confidentiality agreements master confidentiality agreements clinical study agreements and amendment agreements. Work closely with Clinical Operations study team and play a key role to ensure deliverables are in alignment with defined study timelines. Essential functions of the job include but are not limited to Review draft and negotiate a variety of agreements including master services agreements site contracts consulting agreements vendor agreements confidentiality agreements and other client contracts. Work with supervisor and various internal/external key stakeholders to resolve/escalate contractual issues. Ensure adherence to company policies procedures and contracting standards. Update relevant study team members regarding the status of contract negotiations and execution. Establish track report and manage site contract metrics. Support the maintenance of contract files and databases including contract archiving. Assist in designing and implementing policies and procedures to affect the timely execution of contracts. Recognize where processes can be improved and take corrective action. Other tasks as assigned. Qualifications Minimum Required Graduate postgraduate 4-year college degree Experience in a CRO/healthcare field Relevant experience in drafting reviewing and negotiating site Clinical Trial Agreements Vendor Contracts and Site Budget negotiations but no less than 5 years’ experience. Experienced leading interactions with Study Teams and Sponsor Preferred Bachelors in law scientific fields business administration or equivalent degree Excellent organizational and communication skills and attention to detail Knowledgeable on setting up Contracting Plans - Guides for CTA & Budget negotiations Successful handling relationship study team and/or with CRAs/Start-up Associate/(S)BSCA to meet study timelines Skills and Competencies Possesses strong organizational/written communication skills and the ability to multi-task and prioritize in a fast-paced environment. Executes time-sensitive matters while maintaining accuracy and attention to detail. Exhibits high self-motivation and is able to work and plan independently as well as in a team environment. Demonstrates a high degree of professionalism as evidenced by punctuality ability to deliver on commitments an understanding of the service culture and positive interactions with customers and teammates including good interpersonal skills. Displays sound business judgment and a proactive independent work style. Proficient in MS Office software programs and computer applications Handles sensitive issues with discretion. Works well independently and cooperatively with others to achieve common goals in a virtual environment. Develops maintains and strengthens relationships with others inside or outside of the organization who can provide information assistance and support. #LI-TB1 #LI-Remote Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants please also refer to our CA Privacy Notice Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race color age religion sex sexual orientation gender identity national origin disability veteran status or other characteristics protected by law. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying you may contact Precision Medicine Group at myHR@precisionmedicinegrp.com Recruitment Fraud Warning Please be aware that fraudulent individuals and websites may impersonate Precision Medicine Group or its affiliates and attempt to obtain personal financial or banking information through fake job postings or employment offers. Precision Medicine Group will never request payment banking details or other sensitive financial information as part of the recruitment process. If you believe you have been targeted by a recruitment scam we encourage you to report the incident to your local law enforcement authorities consumer protection agency or relevant cybercrime reporting organization in your country. Please also notify us at myHR@precisionmedicinegrp.com so we can investigate and take appropriate action.
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