Offer summary
Qualifications:
Bachelor's degree in Life Sciences, 5-10 years of clinical research experience, Strong knowledge of ICH-GCP and regulations, Excellent decision-making and leadership skills, Proficient in English and relevant IT skills.
Key responsabilities:
- Oversee full lifecycle of clinical trials
- Act as primary contact managing timelines and recruitment
- Prepare and manage trial budgets and contracts
- Ensure timely reporting and compliance checks
- Coordinate cross-functional teams for study conduct