Clinical Research Coordinator

Job Summary:

We are seeking a proactive male Clinical Research Coordinator with 1–2 years of experience in clinical trial coordination. The ideal candidate will assist in the smooth conduct of clinical trials at the site level, ensuring adherence to protocol, GCP, and applicable regulatory standards.

Key Responsibilities:

• Assist in planning and execution of clinical trials under the supervision of the Principal Investigator.
• Coordinate participant screening, recruitment, informed consent, and enrollment.
• Conduct subject visits and ensure protocol procedures, data collection, and documentation are performed accurately and on time.
• Maintain all study-related records, including source documents, CRFs, logs, and investigator files.
• Manage study supplies and investigational product (IP) as per protocol and SOPs.
• Liaise with sponsors, CRAs, and vendors during monitoring visits or audits.
• Ensure safety reporting (AE/SAE) is timely and accurate.
• Coordinate logistics of subject follow-ups and sample shipment, including occasional off-site or late-hour coordination when necessary.
• Support regulatory documentation, submissions, and communications with the Ethics Committee.
• Maintain confidentiality and ethical conduct throughout the study duration.

Required Qualifications:

• Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or equivalent.
• 1–2 years of experience working as a CRC or Clinical Trial Assistant.
• Basic understanding of GCP, clinical trial conduct, and ethics guidelines.
• Good verbal and written communication skills.
• Ability to multitask, maintain accuracy, and work independently.
• Willingness to travel locally and work flexible hours when required.

Desirable Skills:

• Experience in managing Phase II/III clinical trials.
• Familiarity with electronic data capture (EDC) systems.
• Previous interaction with sponsors, CROs, and Ethics Committees.

Job Type: Full-time

Pay: From ₹20,000.00 per month

Benefits:

• Food provided
• Health insurance
• Paid time off
• Provident Fund

Schedule:

• Day shift

Ability to commute/relocate:

• Peenya, Bengaluru, Karnataka: Reliably commute or planning to relocate before starting work (Preferred)

Education:

• Master's (Preferred)

Experience:

• Clinical research: 1 year (Required)

Language:

• English (Required)

Work Location: In person

Application Deadline: 31/07/2025
Expected Start Date: 23/07/2025