KV Clinical Research Hiring For Clinical Research Coordinator

Pharmabharat; Patna; On-site; INR 300,000 - 600,000; Full time

Benefits offered by this job

Exposure to clinical trial management and site coordination

Career growth in clinical operations and research

Professional work environment

Learning opportunities in regulatory and patient management activities

Job summary

KV Clinical Research Pvt Ltd is seeking a Clinical Research Coordinator in Patna, Bihar. The role requires a minimum of 1 year experience in clinical research and relevant educational qualifications including B.Pharm, M.Pharm, or M.Sc in Clinical Research.

The selected candidate will coordinate clinical trial activities, manage patient recruitment, and ensure compliance with regulatory guidelines. Benefits include opportunities for career growth and professional development.

Qualifications

• Minimum 1 year of experience in clinical research.
• Educational background in pharmacy or clinical research.

Responsibilities

• Coordinating clinical trial activities at the research site.
• Managing patient recruitment and follow‑up activities.
• Maintaining clinical trial documentation and regulatory records.
• Ensuring compliance with GCP and protocol guidelines.
• Coordinating with sponsors, CROs, and internal teams.
• Handling informed consent documentation and patient data.
• Supporting audit and monitoring activities.

Skills

Knowledge of clinical trial processes

Understanding of ICH-GCP guidelines

Strong communication and coordination skills

Documentation and reporting expertise

Ability to manage patient interactions professionally

Education

B.Pharm, M.Pharm, Pharm D, Diploma in Clinical Research, M.Sc in Clinical Research

Job description

KV Clinical Research Pvt Ltd – Clinical Research Coordinator (Patna, Bihar)

Job Overview: KV Clinical Research Pvt Ltd is seeking a Clinical Research Coordinator (CRC) located in Patna, Bihar. The position requires a minimum of 1 year of experience in clinical research and an educational background of B.Pharm, M.Pharm, Pharm D, Diploma in Clinical Research, or M.Sc in Clinical Research.

Key Responsibilities

• Coordinating clinical trial activities at the research site
• Managing patient recruitment and follow‑up activities
• Maintaining clinical trial documentation and regulatory records
• Ensuring compliance with GCP and protocol guidelines
• Coordinating with sponsors, CROs, and internal teams
• Handling informed consent documentation and patient data
• Supporting audit and monitoring activities

Eligibility Criteria

• Educational Qualification: B.Pharm, M.Pharm, Pharm D, Diploma in Clinical Research, M.Sc in Clinical Research
• Experience Required: Minimum 1 year in Clinical Research

Preferred Skills

• Knowledge of clinical trial processes
• Understanding of ICH‑GCP guidelines
• Strong communication and coordination skills
• Documentation and reporting expertise
• Ability to manage patient interactions professionally

Benefits of Joining KV Clinical Research

• Opportunity to work in the growing clinical research industry
• Exposure to clinical trial management and site coordination
• Career growth in clinical operations and research
• Professional work environment
• Learning opportunities in regulatory and patient management activities

Application Method

Preferred application: Email.