Offer summary
Qualifications:
University degree in medicine or science, Knowledge of ICH-GCP guidelines, Ability to review and evaluate medical data, Excellent written and verbal English communication, Valid driver's license and willingness to travel.Key responsabilities:
- Oversee and coordinate clinical trials
- Ensure compliance with regulations and protocols
- Collect and analyze critical data
- Maintain study documentation and status reports
- Develop collaborative relationships with stakeholders