11 Biopharmaceutical Leadership jobs in Remote - Czechia.

Hiring now: Qualified Person For Phar @ Parexel, Associate Dir Coa Managem @ Iqvia, Clinical Regulatory Affai @ Syneos Hea, Sr Clinical Proj Mgr @ Novartis.Explore more at jobswithgpt.com.

🔥 Skills

Clinical Trials (7) Data Management (5) Biostatistics (3) Functional Service Provider (2) Regulatory Affairs (2) Statistical Programming (2) Project Management (2) Quality Assurance (2) FSP (2) Qualified Person (1)

📍 Locations

Czechia (11)

Parexel

Skills & Focus: Qualified Person, Pharmacovigilance, Freelancer, Clinical Trials, Functional Service Provider, Clinical Operations, Data Management, Medical Writing, Regulatory Affairs, Biostatistics
About the Company: Parexel is a global leader in providing innovative solutions to accelerate the drug development process for the biopharmaceutical industry.
Type: Freelancer
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.

Iqvia

Skills & Focus: COA Management, Patient Centered Solutions, Clinical Trials, Consulting, Health Technology Assessments, Product Lifecycle Management, Market Access, Research, Stakeholder Engagement, Financial Management
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: 8-10 years total work experience with 5+ years in the pharmaceutical/medical device industry.
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Parexel

Skills & Focus: Clinical Trials, Site Care Partner, Functional Service Provider, CRA, Data Management, Quality Management, Clinical Logistics, Biostatistics, Statistical Programming, Project Leadership

Syneos Health

Skills & Focus: Clinical Trials, Regulatory Pathways, Site Start-Up, Patient Enrollment, Project Management, Clinical Development, Data Management, Vendor Management, Quality Assurance, Project Delivery
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Minimum 6 years CRO industry experience and/or a minimum 5 years’ experience working in a SSU, or clinical trial environment.
Type: Full-time
Benefits: Career development, supportive line management, technical training, peer recognition, total rewards program.

Parexel

Skills & Focus: Clinical Trials, FSP, Czech Republic, Remote, Data Management, Regulatory, Quality Assurance, Clinical Research, Biostatistics, Talent Pool
About the Company: Parexel provides solutions across the entire spectrum of drug development and commercialization.
Type: Full-time

Iqvia

Skills & Focus: FSP, Real-World Evidence, business development, operational oversight, collaboration, Epidemiology, Data Science, Psychometrics, Health Economics, cross-functional
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: 10+ years
Type: Full-time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Novartis

Skills & Focus: Clinical Trials, Project Management, Regulatory Requirements, Data Analysis, Cross-functional Team, Timeline Management, Quality Control, Budget Management, Study Protocols, Good Clinical Practice
About the Company: Novartis is an innovative medicines company. Every day, we work to reimagine medicine to improve and extend people’s lives so that patients, healthcare profess…
Experience: 10+ years of Clinical Operations experience

Iqvia

Skills & Focus: Regulatory Affairs, Russian market, Technical writing, Post-approval, Stakeholders, Regulatory submissions, Health Authority, Lifecycle management, Project management, Regulatory procedures
About the Company: IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed throug…
Experience: At least 5 years relevant experience in lifecycle management regulatory affairs for Russian market
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.
Skills & Focus: statistical programming, clinical data, SAS, ADaM, regulatory requirements, programming activities, CDISC standards, data structure, quality control, exploratory analyses
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: At least 5+ years of experience in either clinical programming and/or statistical programming
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Novartis

Skills & Focus: medical affairs, neuroscience, clinical studies, KOLs, regulatory stakeholders, clinical research, Non Interventional Studies, investigator initiated trial, medical insights, risk identification
About the Company: Novartis is an innovative medicines company. Every day, we work to reimagine medicine to improve and extend people’s lives so that patients, healthcare profess…
Experience: Minimum of 3 years of experience in medical affairs, ideally in neuroscience
Benefits: Company car, Monthly pension contribution matching your contribution up to 3% of your gross monthly base salary, Compan…