Medical Job Opportunity for MD Pharmacology | Apply Now
Medical job seekers with an MD in Pharmacology have an excellent opportunity at Cliantha Research Limited, Ahmedabad. This position offers a dynamic role as a Medical Monitor, contributing to Phase I–IV clinical trials, regulatory processes, and safety monitoring activities. If you are looking for high-growth md jobs in clinical research, this opportunity in Gujarat could be your next career move.
Job Details:
- Job Position: Medical Monitor
- Location: Ahmedabad, Gujarat, India
About the Company:
Cliantha Research Limited is a well-established clinical research organization conducting Phase I to Phase IV clinical trials. The company provides comprehensive clinical research services and works closely with sponsors, regulatory authorities, investigators, and stakeholders to ensure high-quality research and patient safety standards.
Job Description:
This medical job involves providing medical input in protocol design, medical monitoring, and safety monitoring of clinical trials conducted by Cliantha Research Limited (Phase I to IV). The Medical Monitor will be responsible for interacting with Key Opinion Leaders (KOLs) for medical inputs related to feasibility, protocol writing, Data Monitoring Committees, and regulatory requirements. The role also includes regular interactions with the Sponsor’s medical team for preparation of study-related documents and presentations. Therapeutic and protocol training for the project team is an important part of this md job. The candidate will interact with Investigators for patient eligibility and medical monitoring activities. Reviewing efficacy data, safety data, and protocol deviations related to clinical trials is a key responsibility. Reviewing data trends and preparing presentations, as applicable, is also required.
Qualifications:
Key Responsibilities:
- Provide medical input in protocol design and clinical trial monitoring (Phase I–IV)
- Safety monitoring and medical oversight of trials
- Interact with KOLs for feasibility and protocol inputs
- Collaborate with Sponsor’s medical team for study documents and presentations
- Conduct therapeutic and protocol training for project teams
- Interact with Investigators for patient eligibility and monitoring
- Review efficacy data, safety data, and protocol deviations
- Analyze data trends and prepare presentations
- Communicate safety aspects with study teams, sites, regulatory agencies, and sponsors
- Attend regulatory meetings
- Prepare departmental SOPs under guidance
- Assist in medical inputs for RFPs
- Prepare or review regulatory submission documents including RMP and executive summaries
- Handle additional responsibilities assigned by management
