Clinical Trials Associate Project Manager, Apsida Life Science

Report this listing

Solliciteren

Plaats

Ottignies-Louvain-La-Neuve
1340
Waals-Brabant
België

Contract

Vooltijds, Onbepaalde duur

Datum gepubliceerd

2025-06-21

Online to:

2025-08-20
EUR 20.00 HOUR

Clinical Trials Associate Project Manager

Location: Leuven, Belgium (4 days in office, 1 day from home) Job title: Associate Director, Clinical Trial Manager VP of Clinical Operations Apsida Life Science is exclusively partnering with a leading global CRO that is looking to appoint an Associate Director, Clinical Trial Manager to be based in London. The Associate Director Clinical Trial Manager will act as the project lead for multiservice full service global clinical trials. The position interacts with sponsors and manages the timeline and all project deliverables. Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable Manage risk assessment and execution Responsible for management of study vendor Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables Experience in either Oncology, Cardiovascular or GI ~5+ years in a Clinical Trial Manager or Clinical Project Manager position for a full service CRO that is looking to take a step up! Strong healthcare package ~ We believe there is a gap in the market for a cost effective, high quality and trusted recruitment service that puts the candidate journey at the heart of the recruitment process.

Solliciteren