Job Overview
This role involves monitoring clinical trials to ensure compliance with protocols and regulations, as well as managing study-related documentation.
Candidates should possess a strong understanding of Good Clinical Practice (GCP), equivalent to a degree in life sciences or significant relevant experience.
The ideal candidate will have excellent organizational skills, be able to work effectively in a fast-paced environment, and demonstrate a commitment to delivering high-quality results.
Required Skills & Qualifications:
* A degree in Life Sciences or related field;
* Relevant industry experience with Good Clinical Practices;