- Conduct clinical trials and research studies, ensuring compliance with regulatory guidelines.
- Screen, recruit, and enroll study participants, obtaining informed consent.
- Monitor patient health, manage adverse events, and ensure patient safety.
- Collect, analyze, and interpret clinical data accurately.
- Collaborate with cross-functional teams, including data management and biostatistics.
- Prepare and review study protocols, reports, and regulatory documents.
- Maintain high ethical standards and ensure the integrity of research.
- Stay updated with advancements in clinical research and medical practices.
Approach is a platform where the employer and the employee can connect for one goal, Professional Networking. Our user-friendly experience ensures that individuals from different fields can connect to each other with complete transparency and get the... Read More
