Role DescriptionThe Research Physician is a Site based role responsible to serve as Principal Investigator/ Sub Investigator on all clinical trials conducted at the site in compliance with Good Clinical Practice (GCP) , Study Protocols and relevant Standard Operating Procedures (SOPs). The Research Physician is primarily responsible for the overall conduct of the study, ensuring participant safety, ethical research practices, data integrity, and compliance with regulatory guidelines.Primary Responsibilities Medical/Clinical

• Identifying eligible participants, review of inclusion/exclusion criteria, obtaining informed consent, and carefully screening potential subjects to ensure they meet the study criteria.
• Monitoring patient safety- Actively monitoring participants for any adverse events, test results, reporting serious or unexpected events to the appropriate regulatory bodies promptly
• Ensuring the study is conducted ethically, protecting the rights and welfare of participants, and addressing any ethical concerns that arise.
• Patient care and communication
• Drug accountability and dosing of investigational medical products.
• Contemporaneous study data capture

• Identifying eligible participants, review of inclusion/exclusion criteria, obtaining informed consent, and carefully screening potential subjects to ensure they meet the study criteria.
• Monitoring patient safety- Actively monitoring participants for any adverse events, test results, reporting serious or unexpected events to the appropriate regulatory bodies promptly
• Ensuring the study is conducted ethically, protecting the rights and welfare of participants, and addressing any ethical concerns that arise.
• Patient care and communication
• Drug accountability and dosing of investigational medical products.
• Contemporaneous study data captur