Junior Clinical Project Manager
Il y a 3 semaines
Brussels Region, Belgique
Randstad Belgium
Temps plein
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We’re Hiring: Junior Project Manager – Clinical Digital Technology (Hybrid)
Are you a Project Coordinator or Junior PM with experience in
GxP/regulated environments
, looking to step into the fast-paced world of
clinical digital transformation
?
We are looking for a
Junior Project Manager (2–3 years of experience)
to join a global biopharmaceutical team. In this role, you will work closely with experienced Project Leads to coordinate the rollout of digital systems used in clinical trials.
Why this opportunity?
- High-Impact Projects: Work at the intersection of clinical research and digital technology.
- Fast-Track Learning: Progressive autonomy with strong onboarding & mentorship from senior leads. What you’ll do:
- Project Tracking: Update roadmaps, project plans, RAID logs (risks/issues), and delivery calendars.
- Execution & Readiness: Coordinate UAT testing, configuration, cutover, go-live, and hypercare activities.
- Cross-Functional Bridge: Align business stakeholders, IT, Quality, Data Privacy, and external vendors.
- Governance: Prepare status reports, meeting minutes, and executive-level updates. What we’re looking for:
-
Experience:
2 to 3 years in Project Management or Project Coordination ( *0-2 years considered only with strong exposure)
*
- Must-Have Domain
Experience:
Solid background working in a GxP-regulated environment and understanding quality/compliance standards.
- Tech & Tools: Proficient in Microsoft 365 (Excel, Teams, SharePoint) & project tracking tools (Jira, MS Project, or Smartsheet).
- Languages: Advanced English is essential ( *French or Dutch is a plus
* ).
- Soft
Skills:
Exceptional organization, follow-up discipline, and matrix communication. Nice to have:
- Experience in Clinical Trials, Clinical Operations, or solutions like Veeva or Certara .
- Exposure to Computer System Validation (CSV/CSA) or PM Certifications (CAPM, PRINCE2, Agile). Work Model: Full-time | Hybrid (40% on-site) Ready to apply? Send us your application today
- High-Impact Projects: Work at the intersection of clinical research and digital technology.
- Fast-Track Learning: Progressive autonomy with strong onboarding & mentorship from senior leads. What you’ll do:
- Project Tracking: Update roadmaps, project plans, RAID logs (risks/issues), and delivery calendars.
- Execution & Readiness: Coordinate UAT testing, configuration, cutover, go-live, and hypercare activities.
- Cross-Functional Bridge: Align business stakeholders, IT, Quality, Data Privacy, and external vendors.
- Governance: Prepare status reports, meeting minutes, and executive-level updates. What we’re looking for:
-
Experience:
2 to 3 years in Project Management or Project Coordination ( *0-2 years considered only with strong exposure)
*
- Must-Have Domain
Experience:
Solid background working in a GxP-regulated environment and understanding quality/compliance standards.
- Tech & Tools: Proficient in Microsoft 365 (Excel, Teams, SharePoint) & project tracking tools (Jira, MS Project, or Smartsheet).
- Languages: Advanced English is essential ( *French or Dutch is a plus
* ).
- Soft
Skills:
Exceptional organization, follow-up discipline, and matrix communication. Nice to have:
- Experience in Clinical Trials, Clinical Operations, or solutions like Veeva or Certara .
- Exposure to Computer System Validation (CSV/CSA) or PM Certifications (CAPM, PRINCE2, Agile). Work Model: Full-time | Hybrid (40% on-site) Ready to apply? Send us your application today