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 kaamvaam.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

Clinical Research Associate FSP Belgium Zaventem
Skills & Focus: Clinical Research Associate, site selection, monitoring, Good Clinical Practice, subject recruitment, regulatory submissions, data query resolutions, collaborating, organizational skills, communication skills
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: Experience in Pharma Industry, and/or Clinical Trials environment
Type: Full time
Benefits: Company car, mobile phone and attractive benefits packaging.

Sgs

e-CRF Designer Mechelen
Skills & Focus: clinical trial, application, designing, configuring, validating, data collection tools, protocol, programming training, review, validation rules
About the Company: SGS is a leading inspection, verification, testing and certification company.
Medical Monitoring Specialist Mechelen
Skills & Focus: medical monitoring, clinical trials, protocols, medical review, adverse events, safety data, ICSR, literature search, benefit/risk assessment, eCRF
Global Feasibility Associate Mechelen
Skills & Focus: global feasibility, clinical trials, multi-center, RFP analysis, feasibility plan, project questionnaire, kick-off meetings, data collection, outcome report, site assessment

Psi

Medical Monitor Leuven
Skills & Focus: medical input, clinical studies, GCP guidelines, data safety monitoring, clinical development plans, clinical data review, FDA compliance, investigator brochures, risk mitigation, Pharmacovigilance
About the Company: PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners, while always focusing on patients' safety and…

Johnson & Johnson

Associate Director, RA Submissions Beersel
Skills & Focus: regulatory submission, strategic plan, submission management, global registration, dossier planning, global regulatory team, submission strategies, pharmaceutical development, cross-functional teams, health authority guidelines
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 of 8 years of experience in regulatory affairs, submission management, or a related field.
Type: Hybrid
Manager, Feasibility Beersel
Skills & Focus: Feasibility strategy, Clinical Trial Project Management, Stakeholder engagement, Data analytics, Study management, Site activation, Recruitment expectations, Regulatory operations, Clinical research, Operational knowledge
About the Company: Johnson & Johnson is a global healthcare company known for its innovative medicines and medical technologies, committed to improving health for humanity.
Experience: Minimum of 8 years in Pharmaceutical, Healthcare or related industries.
Type: Hybrid
Associate Director, Trial Supply Lead Beersel
Skills & Focus: Clinical Supply Chain, drug management, demand forecasting, supply planning, clinical trials, leadership, compliance, collaboration, project management, GxP principles
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 of 8 years of experience preferably in a supply chain related role.
Type: Hybrid