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HQ - Clinical Quality Assurance Manager
- Permanent
- Good Clinical Practice (GCP)
- France
This vacancy has now expired. Please see similar roles below...
Proclinical are recruiting a HQ - Clinical Quality Assurance Manager for a biotech corporation. This role is on a permanent basis and is located in France.
Responsibilities:
- Serve as a learning management system referent for clinical which involves safety.
- You will distribute critical quality and performance indicators & metrics for clinical quality.
- Consistently improve the clinical and safety SOPs concerning the global legislation which involves FDA/EMA/GVP/ICH guidelines and company policies.
- The ideal candidate will perform spot checks and controls on specific subjects.
- Guarantee audits/inspections promptness which involves any preparation of assistance required for the team and possibly clinical investigator sites.
- Other duties may be assigned to this role.
Key Skills and Requirements:
- Expertise on international GCP guidelines and regulations.
- Know-how and comprehension of pharmaceutical development and pharmaceutical industry guidelines.
- Communication skills both verbally and in writing.
- Able to think systematically and reason with others.
- Analytical capabilities with the ability to work within a logical, structures and organised manner.
- A flexible individual with the ability to adapt to changing assignments.
- Works well independently as well as in a team.
- Fluency in the English and French languages.
- Computer literacy.
If you are having difficulty in applying or if you have any questions, please contact Antoine Mortiaux at +49 6950608631.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
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