A Clinical Research Coordinator position is available in Bangalore for candidates with experience in BA/BE studies. The role focuses on clinical study coordination, CTRI registrations, weekly Ethics Committee (EC) submissions, participant screening, data management, regulatory documentation, and safety reporting.
Job Details
| Job Details | Information |
|---|---|
| Position | Clinical Research Coordinator |
| Experience | 0–3 years |
| Required Experience | BA/BE studies |
| Location | Bangalore BO1 |
| Job Type | Full-Time |
| Education | Bachelor’s degree in Life Sciences or related field |
Position
Clinical Research Coordinator
The Clinical Research Coordinator will assist with planning and coordinating clinical trials under the supervision of the Principal Investigator, while ensuring compliance with study protocols, GCP, and regulatory requirements.
Key Responsibilities
- Assist in planning, initiation, and coordination of clinical trials.
- Manage CTRI registrations accurately and within timelines.
- Prepare, review, and submit Ethics Committee (EC) submissions on a weekly basis.
- Maintain regulatory documentation and track updates and approvals.
- Identify and screen eligible study participants.
- Maintain screening and enrollment logs.
- Facilitate and document the informed consent process.
- Collect, record, and maintain study data accurately.
- Perform routine data quality checks and validations.
- Coordinate with investigative sites and internal teams.
- Assist with regulatory document preparation and submissions.
- Monitor, document, and report adverse events according to regulatory guidelines.
- Support participant safety oversight in collaboration with the study team.
- Participate in ongoing training and stay updated with clinical research regulations and industry trends.
Eligibility and Qualifications
Education
- Bachelor’s degree in Life Sciences or a related field.
Experience
- 0–3 years of experience in BA/BE studies is mandatory.
Required Skills
Candidates should have:
- Strong organizational and multitasking abilities.
- Excellent communication and interpersonal skills.
- High attention to detail and accuracy.
- Good understanding of Good Clinical Practice (GCP) and regulatory requirements.
- Adaptability.
- Ethical conduct.
- Accountability.
- Collaboration.
- Time management.
