Pharmacology Job at Lambda | MD Graduates Apply Now for the Manager Position
Lambda Therapeutic Research Ltd., a leading global Clinical Research Organization (CRO) headquartered in Ahmedabad, is hiring for the role of Manager – Scientific Management, Medical Services. The ideal candidate will be an MD in Pharmacology with hands-on experience in medical monitoring, feasibility assessment, and clinical documentation. This Pharmacology Job offers a dynamic opportunity to contribute to global drug development and clinical research excellence.
- Job Posting: Manager – Scientific Management, Medical Services]
- Location: Ahmedabad, India
- Job ID: 1385
About the Company
Lambda Therapeutic Research is a Global full-service Clinical Research Organization (CRO) with its headquarters in Ahmedabad, India. With facilities and operations strategically located in Mehsana (India), Las Vegas (USA), Toronto (Canada), Barcelona (Spain), London (UK) and Warsaw (Poland), we offer comprehensive end-to-end clinical research services to the global innovator, biotech, and generic pharmaceutical industries.
Experience
1-2 years in Medical Monitoring role.
Qualification for the Pharmacology Job
M.D. Pharmacology
Responsibilities
Feasibility Grid Preparation:
Preparing the feasibility for the Clinical trials as per the requirement of the sponsors. Reviewing Feasibility Questionnaires and feasibility reports.
Medical Writing:
Prepare and review study related documents like Protocol Synopsis, Study Protocols, Investigator’s Brochure, Informed consent forms, Clinical study reports, Patient diaries etc.
Medical Monitoring:
Medical Monitoring at site level is comprised of review of Site Investigator File, Safety and SAE reporting documents, Laboratory documents and reports, X-ray and ECG reports. Medical monitoring performed remotely at Lambda Office comprises of providing guidance, if required by PI/study team, which will include, but not be limited to, eligibility criteria, study procedures and patient continuation and discontinuation. It also comprises of reviewing the adverse events and Serious Adverse Events (SAEs) documents, occurring in the trial and ensure proper recording and reporting of the same.
Training:
Train the study team members of the study protocols and other study related documents. Train the members of the department on the various therapeutic / technical areas Site initiation visits.
General Duties:
Keep abreast with the development in the field of clinical research in India and overseas. Comply with quality initiatives designed by the department.
