MSc Life Science Job at Lambda | Apply Now for the Technical Officer Role
Lambda Therapeutic Research Ltd., a global full-service Clinical Research Organization (CRO), is hiring a Technical Officer in Clinical Data Management at its Ahmedabad location. This role is ideal for M.Pharm or M.Sc. Life Science graduates with up to 3 years of experience in clinical data management, offering exposure to eCRF setup, query management, and medical coding in late-phase clinical trials.
- Job Post: Technical Officer – Clinical Data Management
- Req ID: 1302
- Location: Ahmedabad, India
About The Company
Lambda Therapeutic Research Ltd. 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.
Job Requirements
- Develop eCRF (database setup) for late phase projects
- Create CDM documents (like DMP, DVP, eCCG, etc.)
- Program edit checks as per data validation requirements
- Perform medical coding and Query Management activities
- Sharing of CDM updates with project teams & coordinate with eDC developers
Key Deliverables
- eCRF designing, testing, and training
- Query Management & Coding
- Data Management coordination
Experience
Up to 3 years relevant industry experience in data management activities.
Educational Qualification
- M.Sc. (Life Science)
Salary: INR 3,00,000 – 6,00,000
Why This Role?
This Life Science Job at Lambda is ideal for candidates looking to build a career in clinical data management within a global CRO environment. As a Technical Officer at Lambda Therapeutic Research, you will gain hands-on experience in eCRF setup, query management, medical coding, and coordination of data management activities for late-phase clinical trials. The position offers exposure to industry-standard CDM processes, collaboration with global project teams, and the opportunity to strengthen technical and regulatory skills, making it perfect for M.Pharm or M.Sc. Life Science graduates with up to 3 years of experience who want to advance in clinical research operations.
