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CliniMed Lifesciences, a trusted name in clinical research, is hiring Clinical Research Coordinators in Kolkata. This full-time, on-site role offers fresh graduates (BSc, MSc, or B.Pharm) a gateway into the fast-growing clinical research industry. If you’re passionate about clinical trials and regulatory standards, this is your chance to kickstart your career.
Key Responsibilities
As a Clinical Research Coordinator (CRC), you will:
- Facilitate and coordinate daily clinical trial activities.
- Assist the Principal Investigator (PI) during the informed consent process and clarify participant queries.
- Manage study agreements, contracts, and coordinate approvals.
- Organize and attend sponsor visits (site selection, monitoring, and study close-outs).
- Handle data clarification requests promptly.
- Ensure compliance with protocol, SOPs, GCP, and regulatory requirements.
- Maintain subject screening logs, protocol deviation logs, and enrollment databases.
- Prepare for and support monitoring and auditing visits.
- Collaborate with investigators to address audit findings and implement recommendations.
- Establish and maintain study documentation files.
Required Qualifications
- Freshers only
- Educational background: B.Sc, M.Sc, or B.Pharm
- Strong interest in clinical research and patient care
- Good communication and organizational skills
Benefits of Joining
- Immediate joining opportunity
- Exposure to real-world clinical trial management
- Work closely with experienced PIs and sponsors
- Career growth in the clinical research industry
How to Apply
Interested candidates can send their updated resume to:
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📍 Location: Kolkata (On-site)
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