Associate Clinical Project Manager (ACPM)
MSI Pharma, Sauk Trail Beach, WI, United States
Overview
We are partnered with a large pharmaceutical organisation to support the delivery of global clinical studies. You’ll look for an
AssociateClinicalProjectManager
to support the delivery of global clinical studies. You’ll work closely with Clinical Project Managers to ensure studies are delivered on time, with quality and compliance at the core. This is a great opportunity to grow your clinical project management career in a global, regulated environment.
Location & Engagement
Location: Brussels, Belgium
Engagement: Freelancer, ASAP until end of 2026
Key Responsibilities
Support end-to-end delivery of clinical studies (start-up to close-out)
Maintain an inspection-ready
Trial Master File (TMF)
Coordinate study documentation, timelines, and vendors
Track study progress, metrics, and action items
Support audits, inspections, and quality activities
Help manage study systems (e.g. CTMS, Teams, SharePoint)
Hard Skills
1–2 years’ experience in clinical research (CRA, study coordinator, or similar)
Understanding of
ICH-GCP
and clinical trial processes
Experience with clinical systems (CTMS, TMF tools)
Strong Microsoft Office/Teams skills
Excellent written and spoken
English
Soft Skills
Highly organised with strong attention to detail
Proactive, hands-on, and eager to learn
Clear communicator with strong stakeholder skills
Comfortable working in global, cross-functional teams
Calm under pressure with a solutions mindset
Education
Bachelor’s degree in Life Sciences or related field
(Master’s degree is a plus, not required)
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We are partnered with a large pharmaceutical organisation to support the delivery of global clinical studies. You’ll look for an
AssociateClinicalProjectManager
to support the delivery of global clinical studies. You’ll work closely with Clinical Project Managers to ensure studies are delivered on time, with quality and compliance at the core. This is a great opportunity to grow your clinical project management career in a global, regulated environment.
Location & Engagement
Location: Brussels, Belgium
Engagement: Freelancer, ASAP until end of 2026
Key Responsibilities
Support end-to-end delivery of clinical studies (start-up to close-out)
Maintain an inspection-ready
Trial Master File (TMF)
Coordinate study documentation, timelines, and vendors
Track study progress, metrics, and action items
Support audits, inspections, and quality activities
Help manage study systems (e.g. CTMS, Teams, SharePoint)
Hard Skills
1–2 years’ experience in clinical research (CRA, study coordinator, or similar)
Understanding of
ICH-GCP
and clinical trial processes
Experience with clinical systems (CTMS, TMF tools)
Strong Microsoft Office/Teams skills
Excellent written and spoken
English
Soft Skills
Highly organised with strong attention to detail
Proactive, hands-on, and eager to learn
Clear communicator with strong stakeholder skills
Comfortable working in global, cross-functional teams
Calm under pressure with a solutions mindset
Education
Bachelor’s degree in Life Sciences or related field
(Master’s degree is a plus, not required)
#J-18808-Ljbffr