Clinical Research Doctor (Clinical Investigator)

Veeda CR

2 - 5 years

10 - 15 Lacs

mehsana ahmedabad

Posted:-1 days ago| Platform:

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Skills Required

clinical operations health care services ich-gcp guidelines clinical research doctor activities medical services clinical documentation clinical trials

Work Mode

Work from Office

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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