Clinical Project Associate

Company Description

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

Job Description

AbbVie is seeking a motivated Clinical Project Associate to join our Real World Evidence team in Belgium. In this role, you will manage non-interventional clinical studies across Belgium and Luxembourg, ensuring compliance with approved protocols, procedures, and regulations. 

For your assigned non-interventional studies, you will closely collaborate with the medical affairs team and other functions, to make sure that the study specific milestones are met including but not limited to: site selection, site feasibility, study start-up including Ethics Committee (EC) submission, study follow-up and study close-out.

In this role, you will partner with numerous stakeholders inside and outside the affiliate and build expertise across several core business functions.

The function will be based in Belgium and will report to the Affiliate Real World Evidence Lead (ARWEL).

Tasks & Responsibilities

1. Pre-study activities

• Support the Clinical Project Manager (CPM) in developing the study plan, outlining tasks, timelines, resource allocation needed for study initiation, training and study-specific procedures
• Collaborate with CPM, Medical Managers (MM), Medical Advisors (MA), Medical Science Liaisons (MSL) for an effective site selection process
• In case of Global studies, be the point of contact for Global Medical Affairs (GMA) for the assigned clinical studies
• For Affiliate studies, assist the RWE Manager and CPM in Clinical Research Form (CRF) development
• Ensure that all pre-study activities are performed in a timely manner

2. Study start-up activities

• P