Last updated: 2025-05-08

10 Clinical Operations Management jobs in Brussels.

Hiring now: Clinical Research Associa @ Iqvia, Ecrf Designer @ Sgs, Medical Monitor @ Psi, Associate Dir Ra Submissi @ Johnson Jo.Explore more at jobswithgpt.com. at jobswithgpt.com

🔥 Skills

clinical trials (3) leadership (2) Clinical Research Associate (1) site selection (1) monitoring (1) Good Clinical Practice (1) subject recruitment (1) regulatory submissions (1) data query resolutions (1) collaborating (1)

📍 Locations

Mechelen (4) Beersel (4) Zaventem (1) Leuven (1)
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IQVIA

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…

Clinical Research Associate FSP Belgium

Zaventem

  • Skills: Clinical Research Associate, site selection, monitoring, Good Clinical Practice, subject recruitment, regulatory submissions, data query resolutions, collaborating, organizational skills, communication skills
  • Experience: Experience in Pharma Industry, and/or Clinical Trials environment
  • Type: Full time

SGS

SGS is a leading inspection, verification, testing and certification company.

e-CRF Designer

Mechelen

  • Skills: clinical trial, application, designing, configuring, validating, data collection tools, protocol, programming training, review, validation rules

PSI

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners, while always focusing on patients' safety and…

Medical Monitor

Leuven

  • Skills: medical input, clinical studies, GCP guidelines, data safety monitoring, clinical development plans, clinical data review, FDA compliance, investigator brochures, risk mitigation, Pharmacovigilance

Johnson & Johnson

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…

Associate Director, RA Submissions

Beersel

  • Skills: regulatory submission, strategic plan, submission management, global registration, dossier planning, global regulatory team, submission strategies, pharmaceutical development, cross-functional teams, health authority guidelines
  • Experience: A minimum of 8 years of experience in regulatory affairs, submission management, or a related field.
  • Type: Hybrid