About the Company
We are looking for a motivated MBBS-qualified Physician with hands-on experience in a Clinical Research Organization (CRO) environment to join our Clinical Team.
Key Responsibilities:
Oversee clinical trial conduct in accordance with approved protocols
and regulatory guidelines
Review and apply inclusion/exclusion criteria to assess subject eligibility
Ensure recruitment feasibility and protocol adherence
Monitor subject safety and evaluate response to investigational treatment
Assess, manage, and document adverse events
Obtain and document informed consent prior to study procedures
Conduct protocol-required medical examinations and assessments
Maintain accurate, complete, and inspection-ready study documentation
Ensure compliance with ICH-GCP, sponsor, and regulatory requirements