Lambda Therapeutic Research Ltd., a leading Global Clinical Research Organization (CRO), is hiring skilled professionals for multiple roles in clinical data management, medical writing, and clinical trials monitoring. With a strong global presence across India, USA, Canada, Spain, UK, and Poland, Lambda offers growth-oriented careers for life science graduates.
If you are looking for clinical research jobs in Ahmedabad, this is your chance to join a top CRO delivering end-to-end solutions to the pharmaceutical and biotech industry.
Available Positions
1. Technical Officer – Clinical Data Management
CTC: ₹3,00,000 – ₹6,00,000 per annum
Location: Ahmedabad, India
Key Responsibilities:
- Develop eCRFs and perform database setup for late-phase projects
- Create and maintain CDM documents (DMP, DVP, eCCG, etc.)
- Program edit checks and execute data validation activities
- Perform medical coding and query management
- Coordinate with eDC developers and share CDM updates with project teams
Qualifications:
- M.Pharm (Pharmacology) or M.Sc (Life Sciences)
- Up to 3 years’ relevant experience in clinical data management
2. Research Associate – Medical Writing
CTC: ₹3,00,000 – ₹4,50,000 per annum
Location: Ahmedabad, India
Key Responsibilities:
- Draft and QC clinical trial documents including protocols, ICFs, subject diaries
- Ensure compliance with SOPs and global regulatory requirements
- Coordinate with sponsors, investigators, and IRB/IEC committees
- Prepare and review vernacular translations of ICFs and supportive documents
Qualifications:
- M.Pharm / B.Pharm / Pharm.D
- 0–3 years’ experience in protocol writing or medical writing
3. Clinical Research Associate – Clinical Trials (CTM)
CTC: ₹6,00,000 – ₹10,00,000 per annum
Locations: Bangalore, Hyderabad, Chennai, Ahmedabad, Mumbai, Delhi, Kolkata
Key Responsibilities:
- Conduct study site visits (SSV, SIV, SMV, SCOV)
- Train site staff on protocol and compliance requirements
- Oversee patient recruitment, screening, and follow-up
- Ensure timely availability of study materials and IMP
- Act as a communication link between Lambda and trial sites
- Review source data and maintain updated site files
Qualifications:
- MSc, M.Pharm, B.Pharm, BAMS, BHMS, BDS, or equivalent
- At least 5 years’ pharmaceutical industry experience with minimum 1 year as CRA
Benefits of Working at Lambda Therapeutic Research
- Opportunity to work with a globally recognized CRO
- Exposure to international clinical trials and regulatory frameworks
- Competitive salary packages and career growth opportunities
- Collaborative and research-driven work environment
How to Apply
Application Link for Technical Officer – Clinical Data Management
Application Link for Research Associate – Medical Writing
Application Link for Clinical Research Associate – Clinical Trials (CTM)
