Director, Clinical QA Compliance

vor 2 Wochen

Mainz, Deutschland Proclinical Vollzeit

Proclinical are recruiting a Director, Clinical QA Compliance for a biotech business. This role is on a permanent basis. The client is focused on improving the health of many by creating advanced immunotherapies.

**Responsibilities**:

- Warrant the execution of the clinical development quality plan within the development portfolio.
- To guarantee one aligned approach is taken for executing in assistance of the company's clinical trials, you will handle a team.
- Offer quality oversight.
- Supply QA support to the development establishment by certifying considerable organisation consciousness, such as interrelationship of divisions and business priorities.
- Other duties may be assigned to this role.

**Skills & Requirements**:

- At least 8 years of experience in a GCP setting within pharmaceutical or CRO corporation.
- Knowledge of international guidelines such as FA, EMA, linked to clinical development and post sanction.
- Many years of experience within quality functions, for example: auditing, compliance, etc.
- Educated to a degree level in a life science discipline.
- Familiarity handling international communities.

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.

LI-JG1

QualityAssurance

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