Key Responsibilities:
- Assist in study design, protocol development, and regulatory submissions (IRB/ethics approvals).
- Recruit, screen, and enroll study participants; maintain subject databases.
- Coordinate study logistics (scheduling, data collection, specimen handling).
- Ensure adherence to research protocols, GCP, and institutional policies.
- Prepare reports, maintain documentation, and assist with data analysis.
- Liaise between investigators, sponsors, and participants.
Requirements:
- Bachelor’s degree in science, healthcare, or related field (Master’s preferred).
- Prior research/clinical trial experience preferred.
- Strong organizational, communication, and multitasking skills.
- Knowledge of regulatory guidelines (ICH-GCP, HIPAA, etc.).
Job Type: Full-time
Pay: Rs40,000.00 - Rs70,000.00 per month
Work Location: In person