Clinical Research Coordinator

Core Responsibilities

• Patient Management: Identify, screen, recruit, and consent eligible participants, explaining study details and potential risks/benefits.
• Trial Operations: Oversee day-to-day activities, schedule patient visits, manage study drug accountability, and coordinate departments.
• Data & Documentation: Collect, manage, and ensure the accuracy and security of trial data, maintaining thorough records.
• Regulatory Compliance: Adhere to protocols, FDA, ICH-GCP guidelines, and institutional policies.
• Lab Coordination: Properly label, store, and ship biological specimens (blood, urine) to central labs.
• Team Collaboration: Work closely with PIs, doctors, nurses, and sponsors to report progress and resolve issues.

Key Skills & Requirements

• Strong organizational, time management, and multitasking skills.
• Excellent communication, problem-solving, and attention to detail.
• Knowledge of medical terminology and research regulations.

Job Type: Full-time

Pay: From ₹18,000.00 per month

Ability to commute/relocate:

• Jaipur, Rajasthan: Reliably commute or planning to relocate before starting work (Preferred)

Education:

• Bachelor's (Preferred)

Language:

• English (Preferred)

Location:

• Jaipur, Rajasthan (Preferred)

Work Location: In person