Clinical Trials Coordinator
6 months ago
As a Clinical Trials Coordinator, you will play a crucial role in the planning, execution, and monitoring of clinical trials conducted within our organization. This position offers an exciting opportunity for individuals with a strong interest in clinical research to gain hands-on experience in a dynamic and collaborative environment.
**Responsibilities**:
- Assist in the development and review of study protocols, ensuring compliance with regulatory guidelines and ethical standards.
- Collaborate with cross-functional teams to identify study objectives, endpoints, and inclusion/exclusion criteria.
- Prepare regulatory submissions and assist in obtaining necessary approvals from regulatory authorities and ethics committees.
- Organize and conduct study initiation meetings, investigator training sessions, and site visits as needed.
- Monitor study progress, ensuring adherence to protocol requirements, Good Clinical Practice (GCP) guidelines, and study timelines.
- Collaborate with safety monitoring committees and medical monitors to ensure appropriate management of participant safety throughout the trial.
**Qualifications**:
- Master’s or Bachelor's degree in pharmacy/life sciences is required.
- Experience: 0-1 Year
- Strong organizational skills and attention to detail.
- Excellent communication and interpersonal skills.
- Ability to work effectively in a team environment and collaborate with cross-functional stakeholders.
- Familiarity with Good Clinical Practice (GCP) guidelines and regulatory requirements for clinical research is preferred.
**Job Types**: Full-time, Permanent
Pay: ₹15,000.32 - ₹42,109.50 per month
Schedule:
- Day shift
- Morning shift
Supplemental pay types:
- Performance bonus
- Yearly bonus
**Experience**:
- total work: 1 year (preferred)
Work Location: In person
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