20 Clinical Data And Biostatistics jobs in Remote - Republic of Poland.

Hiring now: Study Ops Mgr Spain Fsp @ Parexel, Srprincipal Clinical Data @ Precision , Srprincipal Clinical Data @ Precision , Sr Statistical Programmer @ Syneos Hea, Global Trial Mgr Late Pha @ Iqvia.Explore more at jobswithgpt.com.

🔥 Skills

clinical trials (6) Data Management (5) clinical research (5) programming (5) project management (5) Clinical Trials (4) EDC vendor (4) CDISC standards (4) Good Clinical Practice (4) Clinical Research (3)

đź“Ť Locations

Republic of Poland (20)
🔍 Go to full job search

Parexel

Study Operations Manager - Spain - FSP Republic of Poland
Skills & Focus: Clinical Research, FSP, Remote, CRA, Biostatisticians, Clinical Trials, Project Leaders, Data Managers, Regulatory Consultants, Statistical Programmers
Clinical Programmer (FSP) Republic of Poland
Skills & Focus: Clinical Programming, SQL, Data Review, Statistical Programming, Clinical Trials, Data Management, Biotechnology, Life Sciences, Software Development, eClinical Solutions
About the Company: Parexel supports clinical studies across the full range of therapeutic areas, with longstanding partnerships with a vast client base. The company undertakes vi…
Experience: Minimum of 5 years of experience in developing software in a clinical trial environment using SQL, including at least 3 years of clinical programming experience.
Type: Remote
Benefits: Provides an open and friendly work environment where we empower people and offer opportunities for career advancement.

Precision For Medicine

Senior/Principal Clinical Database Manager Republic of Poland
Skills & Focus: clinical database management, clinical research, data management, EDC vendor, programming, scripting, CDISC standards, object-oriented programming, clinical research tasks, biomarkers
About the Company: 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 us…
Experience: Experience in developing and customizing clinical data management databases in a clinical, scientific or health care discipline; Medidata Rave EDC Certified Study Builder; Rave API integration experience.

Parexel

Clinical Research Associate Republic of Poland
Skills & Focus: Clinical Research Associate, monitoring duties, clinical trials, protocols, regulatory submissions, oncology studies, ICH GCP compliance, site management, independent monitoring, flexible work arrangements
About the Company: Parexel is a global leader in biopharmaceutical services, helping customers maximize their chances of success in clinical research and market access.
Experience: Minimum of 3 years of active independent field monitoring experience.
Type: Remote
Benefits: Premium salary, car or car allowance, paid holidays, medical care plan: Health, Dental & Vision, life assurance.
Clinical Data Analyst Republic of Poland
Skills & Focus: Clinical Data, Data Management, Biostatistics, Clinical Research, Medical Trials, Statistical Programming, Project Leadership, Functional Service Provider, Clinical Operations, Health Improvement
About the Company: Parexel provides a range of services to the biopharmaceutical industry, specializing in clinical research.

Precision For Medicine

Senior/Principal Clinical Database Manager Republic of Poland
Skills & Focus: Clinical Database Manager, clinical data management, EDC vendor, Medidata Rave, Rave API, programming, scripting, CDISC standards, drug development, clinical research
About the Company: 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 us…
Experience: Must have experience in developing and customizing clinical data management databases in a clinical, scientific or health care discipline

Precision Medicine Group

Senior/Principal Clinical Database Manager Republic of Poland
Skills & Focus: clinical databases, Data Management, EDC vendor, operational training, programming, clinical research, Object Oriented Programming, scripting language, CDISC standards, database management systems
About the Company: 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 us…

Syneos Health

Sr Statistical Programmer- PK/PD Republic of Poland
Skills & Focus: SAS, programming, clinical trials, statistical analysis, data listings, quality standards, validation, documentation, project management, mentoring
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Extensive programming experience in SAS or other required software, preferably in a clinical trial environment.

Precision Medicine Group

Senior Clinical Data Manager/Principal Clinical Data Manager Republic of Poland
Skills & Focus: Data Management, Clinical Trials, Database Development, Quality Control, Data Entry, Clinical Protocol, Training, Documentation, Medical Coding, SOP Development
Experience: Bachelors and/or a combination of related experience; Must have worked as a Lead Data Manager for a Clinical Research Organisation or Pharmaceutical company

Syneos Health

Senior Clinical Research Associate I (Sr CRA I) Republic of Poland
Skills & Focus: site qualification, monitoring, regulatory compliance, Good Clinical Practice, patient safety, clinical data integrity, communication, project management, investigator meetings, audit readiness
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience

Iqvia

Global Trial Manager, Late Phase Studies, Single-Sponsor Dedicated Republic of Poland
Skills & Focus: clinical trials, study management, Vendor Management, project management, patient outcomes, data management, healthcare intelligence, protocol development, regulatory documents, Good Clinical Practice
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industri…
Experience: 2-5 years of experience in managing late phase clinical trials at global level
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Precision For Medicine

Senior/Principal Clinical Database Manager Republic of Poland
Skills & Focus: clinical databases, EDC vendor, Data Management, Project Management, programming, scripting, Microsoft Office, clinical research, data management, leadership
About the Company: 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 us…
Experience: Must have experience in developing and customizing clinical data management databases in a clinical, scientific or health care discipline.

Iqvia

Tactical and Operational Scientific Co-Ordinator - Patient Centered Solutions, … Republic of Poland
Skills & Focus: clinical trials, project management, study management, clinical research, customer satisfaction, risk management, collaboration, financial success, communication, problem solving
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industri…
Experience: 5 years of prior relevant experience including > 1 year project management experience
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Precision For Medicine

Drug Safety Physician Republic of Poland
Skills & Focus: pharmacovigilance, safety reporting, clinical support, risk management, signal detection, safety data management, adverse events, compliance, drug safety, clinical trials
About the Company: Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumors on a molecular level usi…
Experience: Minimum of 7 years in Drug Safety related activities in pharma/biotech.

Iqvia

Senior Statistical Programmer Republic of Poland
Skills & Focus: SAS programming, clinical trial, ADaM datasets, TFL, statistical analysis, programming specifications, data import, quality control checks, Good Clinical Practice, ICH guidelines
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: 5+ years in Statistical Programmer role from CRO/Pharma with ADaM and TFL
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Precision Medicine Group

Senior Clinical Data Manager/Principal Clinical Data Manager Republic of Poland
Skills & Focus: Clinical Data Management, Clinical Trials, Database Development, Data Quality, Medical Coding, Data Entry, SOPs, EDC, CRF Specifications, Quality Control
Experience: Minimum Required: Bachelors and/or a combination of related experience
Type: Remote
Senior Clinical Data Manager Republic of Poland
Skills & Focus: Clinical Data Manager, Clinical trial data management, Database development, Data entry quality, CRF specifications, Quality control, SOPs, CDISC standards, Medical coding, Clinical research tasks
About the Company: Precision Medicine Group is an Equal Opportunity Employer focusing on innovative solutions in clinical development and other healthcare services.
Experience: 8+ years’ experience with strong Oncology and/or Orphan Drug therapeutic experience
Type: Full-time

Syneos Health

Principal/Sr Regulatory Medical Writer Republic of Poland
Skills & Focus: Regulatory Affairs, Medical Writing, Clinical Research, Biopharmaceutical, Project Management, Technical Documentation, Clinical Study Protocols, IND Submissions, NDA, ICH Regulations
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.
Experience: Bachelor of Science degree with relevant writing experience or Bachelor of Arts degree (Social Sciences, English or Communications, preferred) with relevant scientific and/or medical knowledge and expertise.

Iqvia

TMF Manager, sponsor-dedicated Republic of Poland
Skills & Focus: TMF, document management, compliance, clinical operations, inspection readiness, Good Clinical Practice, data protection legislation, project management, clinical trials, documentation standards
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: Minimum 6 years of experience with document management systems and excellent understanding of system structures and generic document management functionality.
Type: Full-time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Syneos Health

CRA II / Sr CRA I Republic of Poland
Skills & Focus: Clinical Research Associate, GCP, Site Management, Clinical Trial, Monitoring, Protocol Compliance, Informed Consent, Query Resolution, Pharmacovigilance, Data Integrity
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience.