8 Clinical Data And Biostatistics jobs in Amsterdam.

Hiring now: Sr Analyst Regulatory Med @ Johnson Jo, Sr Clinical Research Asso @ Psi, Clinical Research Associa @ Iqvia, Dir Sr Dir Clinical Outco @ Shionogi, Sr Clinical Research Asso @ Syneos Hea.Explore more at jobswithgpt.com.

🔥 Skills

clinical documents (2) cross-functional teams (2) Clinical Trials (2) Monitoring (2) medical writing (1) regulatory submissions (1) document planning (1) mentorship (1) communication skills (1) scientific experience (1)

📍 Locations

Leiden (4) Amsterdam (4)

Johnson & Johnson

Skills & Focus: medical writing, clinical documents, regulatory submissions, cross-functional teams, document planning, mentorship, communication skills, scientific experience, timelines, leadership
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Experience: At least 6 years of relevant pharmaceutical/scientific experience including at least 4 years of regulatory medical writing experience.
Type: Fully Remote
Skills & Focus: Labeling, Clinical Trials, Regulatory Affairs, Safety Information, Process Improvements, Communication, Collaboration, Performance Indicators, Documentation, Pharmaceutical
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Experience: A minimum 3 years of experience supporting labeling development, implementation, and/or operations within the Pharmaceutical industry.
Type: Hybrid
Skills & Focus: regulatory, clinical data, submissions, data management, biostatistics, programming, compliance, SDTM, ADaM, GCP
About the Company: Johnson & Johnson is a healthcare company dedicated to innovating solutions and improving health for humanity.
Experience: At least 6 years of relevant pharmaceutical/scientific experience
Type: Hybrid
Benefits: Competitive salary and extensive benefits package with a flexible working environment

Psi

Skills & Focus: Clinical Research, Monitoring, SIV, RMV, COV, CRF review, Source document verification, Site communication, Feasibility research, Regulatory support

Iqvia

Skills & Focus: clinical research, monitoring, protocol training, site management, GCP knowledge, communication, life sciences, healthcare, drug indications, career development
About the Company: IQVIA is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients.
Experience: 12 months of independent on-site monitoring experience
Type: Full time
Benefits: Excellent salary and benefits package, company car or car allowance, flexible working hours, genuine career development…

Shionogi

Skills & Focus: Clinical Outcomes Assessment, COA Strategy, Development, Implementation, Patient-Centred Endpoints, FDA’s PRO guidance, PFDD guidance, Project Management, Patient Advocacy, Rare Diseases
About the Company: At Shionogi, we are dedicated to improving global health and well-being. As a leading pharmaceutical company, we are committed to innovation, excellence, and m…
Experience: Highly experienced and strategic individual with expertise in COA-related strategies in the pharmaceutical industry with experience of developing de novo COAs.

Syneos Health

Skills & Focus: Clinical Research Associate, Site Management, ICH-GCP, Regulatory Compliance, Monitoring, Clinical Trials, Clinical Development, Patient Safety, Data Integrity, Investigator Meetings
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Solid monitoring experience in The Netherlands
Type: Hybrid