Lambda Therapeutic Research Ltd., a leading global clinical research organization (CRO) headquartered in Ahmedabad, invites applications for the role of Technical Officer in Clinical Data Management.
This position offers a unique opportunity to contribute to global late-phase clinical trials, ensuring data accuracy and compliance in alignment with international research standards.
If you’re passionate about clinical data management, medical coding, and eCRF design, this role provides a strong foundation for a rewarding career in the clinical research industry.
Key Responsibilities
As a Technical Officer – Clinical Data Management, you will be responsible for:
- Designing and validating electronic Case Report Forms (eCRFs).
- Performing data validation, query management, and database updates.
- Supporting medical coding for concomitant medication data captured in eDC systems.
- Preparing and maintaining clinical data management (CDM) documentation.
- Assisting in planning, execution, and closeout of late-phase clinical trials.
- Conducting and participating in CDM-related trainings and audits.
Educational Qualifications
Applicants should have one of the following qualifications:
- M.Pharm
- M.Sc. (Life Sciences / Clinical Research)
- BDS, BHMS, or BAMS
Experience Required
- Up to 2 years of experience as a Clinical Research Coordinator (CRC) or Data Manager / Data Validator.
- Hands-on experience working on eDC platforms and late-phase clinical trials is desirable.
Key Skills
- eCRF Design & Testing
- Query Management & Medical Coding
- CDM Documentation
- Knowledge of GCP and CDISC Standards
- Strong Analytical and Communication Skills
Why Join Lambda Therapeutic Research
- Exposure to global multi-center clinical trials
- Work with advanced data management tools
- Opportunity for career growth in a top-tier CRO
- Collaborative, research-driven work environment
How to Apply

