Clinical Research Doctor (Clinical Investigator)

2 - 5 years

10 - 15 Lacs

Posted:-1 days ago| Platform: Naukri logo

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Job Type

Full Time

Job Description

Key Responsibilities (JD)

Medical Oversight & Study Conduct

  • Serve as the Principal/ Sub-Investigator for clinical trials in accordance with study protocols, ICH-GCP guidelines, and regulatory standards.
  • Conduct comprehensive medical assessments, physical examinations, and ensure participant eligibility.
  • Oversee participant safety throughout the study, including review of adverse events and clinical data.

Clinical Trial Execution

  • Ensure accurate and timely documentation in source notes, CRFs, and study documentation.
  • Collaborate with cross-functional teams (Clinical Operations, QA, Data Management, Pharmacovigilance) to ensure smooth study execution.
  • Participate in protocol review, feasibility checks, and study set-up processes.

Quality & Compliance

  • Ensure adherence to SOPs, study protocols, and regulatory requirements throughout the clinical trial lifecycle.
  • Support audits, inspections, and quality-improvement initiatives.
  • Maintain updated knowledge of GCP, regulatory norms, and therapeutic guidelines.

Stakeholder Interaction

  • Communicate effectively with sponsors, monitors, ethics committees, and internal teams.
  • Provide medical training and study-related guidance to clinical staff as needed.

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Veeda CR

Clinical Research, Biotechnology

Los Angeles

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