Fortis is seeking a Clinical Research Coordinator to join their team in New Delhi. This position is suitable for candidates with 0-3 years of experience who are eager to start or advance their career in clinical research.
Key Responsibilities
- Coordinate Clinical Research Activities: Oversee the day-to-day operations of clinical trials, ensuring all activities are conducted per protocols and regulatory requirements.
- Compliance: Ensure adherence to study protocols, regulatory guidelines, and Good Clinical Practice (GCP).
- Participant Recruitment: Recruit and screen potential study participants, ensuring eligibility and obtaining informed consent.
- Data Management: Collect, manage, and ensure the integrity of clinical trial data.
- Regulatory Documents: Prepare, submit, and maintain all necessary regulatory documents required for the trial.
- Monitoring: Track study progress and report findings to the research team and sponsors.
- Liaison: Act as the main point of contact between research teams, sponsors, and regulatory bodies.
Candidate Profile
- Experience: 0-3 years in clinical research or related fields.
- Education: A degree in Life Sciences, Pharmacy, Nursing, or a related discipline is preferred.
- Skills: Strong organizational, communication, and interpersonal skills; attention to detail; ability to work collaboratively in a team.
