Regulatory Affairs Consultant

3 weeks ago


Manama, Bahrain RAY-CRO Full time

**Role Description**

This is a part-time remote role for a Regulatory Affairs Consultant. The Regulatory Affairs Consultant will be responsible for providing advice on all aspects of regulatory affairs for clinical trials and marketing authorizations, developing and reviewing regulatory documents (e.g. protocols, investigator brochures, informed consent forms, safety reports, and regulatory submissions), tracking regulatory submission and approval process, and ensuring regulatory compliance and strategy for assigned products.

**Qualifications**
- Bachelor's degree or higher (e.g. Pharmacy) or a related field.
- Minimum of 5 years of regulatory affairs experience in the pharmaceutical.
- Knowledge of international regulations and guidelines (e.g. FDA, EMA, ICH).
- knowledge of product registration and license-holding services in Bahrain.

Residency: Bahrain

Type of contract: Part Time/Freelance

**Job Types**: Part-time, Temporary, Contract



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