MPharm Job at Lambda Therapeutic Research | Apply Now for the Technical Officer Role
Lambda Therapeutic Research Ltd., a prominent Global CRO, is hiring a Technical Officer to specialize in Clinical Data Management (CDM) at its Ahmedabad facility. This MPharm Job is ideal for graduates with a BDS, BHMS, BAMS, M.Pharm, or M.Sc. (Life Sciences/Clinical Research). The officer will be actively involved in late-phase clinical trials, responsible for eCRF designing, data validation, query management, and medical coding of concomitant medication data captured in the electronic Data Capture (eDC) system.
- Job Title: Technical Officer
- Req ID: 1439
- Location: Ahmedabad, India
About The Company
Lambda Therapeutic Research is a full-service Global Clinical Research Organization (CRO) headquartered in Ahmedabad, India. The company offers comprehensive end-to-end clinical research services to the global innovator, biotech, and generic pharmaceutical industries. With strategic facilities and operations spanning multiple continents, including North America, Europe, and Asia, Lambda is a key global partner known for its expertise in various aspects of clinical trials, including meticulous Clinical Data Management (CDM) to ensure data quality and integrity.
Officer Job Details
- Clinical Data Management activities e.g., eCRF designing, Data Validation, Query Management, Training, etc.
- Active involvement in late phase clinical trials – planning, execution and close-out phase activities.
- Medical coding for concomitant medication data captured in the eDC.
Key Deliverables
- eCRF development, testing and updates.
- Query Management.
- Medical Coding.
- CDM documentation.
Education required for the Officer Job
- M.Pharma.
- M.Sc. Clinical Research
Experience
- Up to 2 yrs experience of working as Clinical Research Coordinator (CRC) on eDC platforms.
- Experience of working with CDM department as Data Manager / Data Validator.
Why This Role?
This Technical Officer role at Lambda Therapeutic Research is an excellent entry point into the highly specialized and in-demand field of Clinical Data Management (CDM) within a global CRO setting. As a specialist in CDM, you will gain hands-on expertise in critical processes like eCRF designing, data validation, and medical coding while actively contributing to late-phase clinical trials. This exposure to international standards and sophisticated eDC platforms provides a valuable skill set essential for a long-term career in pharmaceutical research and data integrity.
