Contribute in building a strategically sound local quality plan to ensure our clinical trials will be delivered to the highest quality standards and are following all applicable SOP's, laws and regulations
Job Summary
Contribute in building a strategically sound local quality plan to ensure our clinical trials will be delivered to the highest quality standards and are following all applicable SOP's, laws and regulations.
Be the go-to person for risk management and provide advice for complex situations to ensure timely resolution of issues.
You will be part of a hardworking, enthusiastic, and committed team of +/- 170 people eager to deliver and helping to improve the lives of millions of patients.
Matching Summary
Contribute in building a strategically sound local quality plan to ensure our clinical trials will be delivered to the highest quality standards and are following all applicable SOP's, laws and regulations.
Skills & Requirements
Must-have
GCP, local laws, and regulations
Quality and Compliance Oversight
Local regulatory intelligence
Risk management and advice
Process improvement initiatives
Nice-to-have
Strong communicator, leader, team player
Quick learning and problem-solving abilities
Willingness to engage with authorities
Enthusiastic and committed team
Key Requirements
BA/BS degree in Life Sciences or related scientific field (or 8-10 years equivalent experience)
Minimum of 6 years pharmaceutical industry experience
At least 4-6 years GxP experience in clinical research/quality assurance
Proficient in Dutch, English and French (for Belgian candidates)