13 Clinical Data And Biostatistics jobs in Prague.

Hiring now: Regulatory Affairs Mgr Cm @ Parexel, Pv Officer @ Primevigil, Pharmacovigilance Analyst @ Iqvia, Medical Monitor @ Psi, Lead Local Trial Mgr @ Johnson Jo, Medical Reviewer I @ Ergomed, Site Activation Mgr @ Syneos Hea.Explore more at jobswithgpt.com.

šŸ”„ Skills

project management (4) Clinical Research (3) Data Management (3) Statistical Programming (3) Biostatistics (2) Individual Case Safety Reports (2) Clinical Programmer (2) Pharmacovigilance (2) Clinical Trials (2) regulatory requirements (2)

šŸ“ Locations

Prague (13)
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Parexel

Regulatory Affairs Manager - CMC Biologics Prague
Skills & Focus: Regulatory Affairs, CMC, Biologics, Project Leadership, Clinical Research, Data Management, Statistical Programming, Consulting, Medical Writing, Biostatistics
About the Company: Parexel is a global biopharmaceutical services organization that provides a range of services to enhance the clinical development of drugs and medical devices.
Type: Full-time

Primevigilance

PV Officer Prague
Skills & Focus: case processing, pharmacovigilance, Individual Case Safety Reports, SAE/SUSAR Management, database outputs, PBRER, DSUR, PADER, mentoring, training
About the Company: At PrimeVigilance, PV Officers are independent case processing team members who are expected to manage a variety of case processing services with full accountaā€¦
Experience: Demonstrated experience in case processing.

Parexel

Clinical Programmer (FSP) Prague
Skills & Focus: Clinical Programmer, data review, trial management, SQL, programming, clinical trial, data reporting, Biotechnology, Pharmaceutical, Life Sciences
About the Company: Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base. We supported the tā€¦
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.

Iqvia

Pharmacovigilance Analyst (Contract) Prague
Skills & Focus: Pharmacovigilance, Compliance, Data Entry, Safety Cases, Market Research, Analyses, Client Management, Reporting, Safety Data, Training
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrieā€¦
Experience: Working knowledge of pharmacovigilance requirements and processes.
Type: Contract
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Parexel

Clinical Programmer (FSP) Prague
Skills & Focus: Biostatistics, Statistical Programming, Data Management, Clinical Trials, Procurement, Clinical Research, Clinical Programmer, Remote Work, Global Clinical Operations, Research Organization
About the Company: Parexel is a global clinical research organization that provides comprehensive drug development services to the pharmaceutical and biotechnology industries.
Type: Remote
Clinical Programmer (FSP) Prague
Skills & Focus: Data Management, Clinical Programming, Remote, FSP, Biomedical Research, Clinical Trials, Data Acquisition, Statistical Programming, Global Inclusion, Biometrics

Psi

Medical Monitor Prague
Skills & Focus: Medical point of contact, clinical trials, GCP guidelines, data safety monitoring, clinical development plans, clinical data review, mitigation strategies, safety monitoring boards, compliance, Pharmacovigilance
About the Company: Medical Monitors provide medical input to global clinical studies and advise the teams and business partners, while always focusing on patients' safety and welā€¦

Johnson & Johnson

Lead Local Trial Manager Prague
Skills & Focus: clinical trial management, data generation, protocol oversight, Good Clinical Practice (GCP), regulatory requirements, site selection, budget forecasting, adverse events, project planning, vendor services
About the Company: Johnson & Johnson is a global leader in the healthcare sector, committed to innovation in areas such as pharmaceuticals, medical devices, and consumer health pā€¦
Experience: At least 4 years of clinical trial management experience or more than 6 years of clinical monitoring experience.
Type: Full-time

Ergomed

Medical Reviewer I Prague
Skills & Focus: medical review, Individual Case Safety Reports, Serious Adverse Event, signal detection, literature review, aggregate reports, causality assessment, Periodic Safety Update Reports, Development Safety Update Reports, safety related findings

Iqvia

Associate Design Analytics Lead Prague
Skills & Focus: data analysis, protocol assessments, stakeholder engagement, clinical research, report writing, project management, presentation skills, innovation, data storyboards, healthcare intelligence
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industriā€¦
Experience: Approximately 3 years of relevant experience in clinical research or an equivalent combination of education, training, and 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.
Design Analytics Lead Prague
Skills & Focus: data analysis, clinical research, protocol assessments, stakeholder communication, project management, training and mentoring, insights generation, reports development, process improvements, empirical data
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrieā€¦
Experience: Approximately 3-5 years of relevant experience in clinical research or an equivalent combination of education, training, and 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.
Clinical Research Associate Sponsor Dedicated Prague
Skills & Focus: Clinical Research, monitoring, site selection, regulatory requirements, Good Clinical Practice, project management, data integrity, collaboration, Czech, English
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrieā€¦
Experience: Experience as a Clinical Research Associate for almost two years.
Type: Full time
Benefits: Company car, mobile phone and attractive benefits package

Syneos Health

Site Activation Manager Prague
Skills & Focus: Site Start-Up, clinical trial processes, regulatory activities, project management, patient enrollment, risk management, vendor management, negotiating skills, quality-driven, problem-solving skills
About the Company: Syneos HealthĀ® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medā€¦
Experience: Project management experience in a fast-paced environment.
Type: Hybrid
Benefits: Career development and progression; supportive and engaged line management; technical and therapeutic area training; peā€¦