We are a leading executive search firm supporting a fast-growing listed bio & medical device company with innovative regenerative medicine technology. The client is actively expanding global clinical pipelines and strengthening its R&D and regulatory capabilities.

We are seeking an experienced Clinical Research Associate (CRA) to join their clinical operations team. This role offers the opportunity to lead global IDE/IND trials and collaborate with international partners across multi-center studies.

Clinical Research Associate (CRA)

Key Responsibilities

• Plan and manage domestic and international clinical trials (pharmaceuticals & medical devices).
• Prepare and review clinical trial documentation; manage submissions to regulatory authorities/IRBs (IDE/IND).
• Manage investigators, clinical sites, and collaborate with overseas partners.
• Ensure compliance with GCP/SOP standards; oversee study timeline and budget.

Qualifications

Must-Have:

• Bachelor’s degree or higher.
• 4–8 years of CRA experience in clinical research.
• Native-level English communication skills.
• Hands-on experience in pharmaceutical or medical device clinical trials.

Nice-to-Have:

• Prior work experience in global CROs.
• Proven track record in IDE/IND documentation.

Why Join

• Opportunity to lead global IDE/IND trials with innovative pipelines.
• Exposure to international regulatory frameworks (EU MDR, FDA, PMDA).
• Career growth in a company at the forefront of next-generation regenerative medicine.Please contact
  careerplan@careerplan.be