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Current Openings

Explore exciting opportunities to grow your career with Infoclin LLP.

Clinical Research Coordinator (CRC)

Full-time

Kolkata, West Bengal | Clinical Operations | 2-4 Years Exp.

We are seeking a highly motivated Clinical Research Coordinator to manage and conduct clinical trials in accordance with GCP guidelines and study protocols.

Key Responsibilities:
  • Patient recruitment, screening, and enrollment.
  • Collection and maintenance of study data and source documentation.
  • Ensuring regulatory compliance and ethical conduct of trials.
  • Coordination with investigators, sponsors, and ethics committees.
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Regulatory Affairs Specialist

Full-time

Delhi, India | Regulatory Affairs | 3-5 Years Exp.

An experienced Regulatory Affairs Specialist is needed to ensure compliance with national and international regulations for clinical trial submissions and approvals.

Key Responsibilities:
  • Prepare, review, and submit regulatory documents (e.g., CTAs, amendments).
  • Liaise effectively with regulatory authorities (e.g., DCGI, Ethics Committees).
  • Monitor and interpret changes in regulatory guidelines and ensure compliance.
  • Provide regulatory guidance to internal teams and clients.
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