Clinical Research Coordinator

Job Summary:

We are looking for an experienced and proactive Project Coordinator to join our Clinical Research Department. The ideal candidate will have 5–6 years of relevant experience in coordinating clinical research projects, ensuring they are executed efficiently, within timelines, and in compliance with regulatory and organizational standards

Key Responsibilities:

1. Study Coordination: Manage daily activities of clinical trials, ensuring compliance with Good Clinical Practice (GCP) and regulatory requirements.

2. Site Management: Develop and maintain relationships with study sites, investigators, and staff.

3. Regulatory Compliance: Ensure compliance with regulatory requirements, including IRB/IEC submissions and approvals.

4. Data Management: Oversee data collection, management, and quality control.

5. Communication: Facilitate communication among study sites, sponsors, and other stakeholders.

6. Problem-Solving: Identify and resolve issues that arise during the study.

7. Documentation: Maintain accurate and complete study documentation.

Requirements:

1. Education: Bachelor's degree in a life science, nursing, or related field.

2. Experience: 5 to 6 experience in clinical research coordination.

3. Skills: Strong organizational, communication, and problem-solving skills.

4. Knowledge: Familiarity with GCP, regulatory requirements, and clinical trial operations.

Desirable Skills:

1. Certification: Certification in clinical research coordination (e.g., CCRA or CCRC).

2. Experience with Clinical Trial Management Systems (CTMS): Familiarity with CTMS and electronic data capture (EDC) systems.

Job Types: Full-time, Permanent

Pay: ₹45,000.00 - ₹50,000.00 per month

Benefits:

• Food provided
• Health insurance
• Provident Fund

Schedule:

• Day shift
• Fixed shift

Work Location: In person

Application Deadline: 20/07/2025