Build Your Career with Lambda Therapeutic Research Ltd: Manager – Report Writing
If you’re looking for rewarding MD pharmacology jobs and want to work with a global CRO, the Manager – Report Writing position at Lambda Therapeutic Research Ltd in Ahmedabad is a strong opportunity. This role offers hands-on experience in Clinical Study Report authoring, regulatory submissions, and late-phase clinical projects—ideal for candidates seeking high-impact jobs in Ahmedabad within the clinical research domain.
- Job Title: Manager – Report Writing
- Req ID: 1403
- Location: Ahmedabad, India
- CTC Range (INR): 12,00,000 – 16,00,000
Qualifications:
Educational Qualification: MD Pharmacology
This makes the role an excellent match for individuals exploring md pharmacology jobs in the clinical research sector.
Experience Required to join Lambda Therapeutic Research Ltd:
- 0 – 1 year experience in Clinical Study Report writing for Late Phase projects
- Trainings on medical writing, CSR writing, literature search, etc.
This entry-level requirement makes it one of the most promising jobs in Ahmedabad for early-career medical writing professionals.
About the Lambda Therapeutic Research Ltd:
Lambda Therapeutic Research Ltd is a Global full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India. With facilities and operations operating in Mehsana (India), Las Vegas (USA), Toronto (Canada), Barcelona (Spain), London (UK), and Warsaw (Poland), the organization offers complete end-to-end clinical research services worldwide. This makes it a strong employer for professionals searching for MD pharmacology jobs and high-quality jobs in Ahmedabad.
Job Description:
The Manager – Report Writing role involves the authoring of Clinical Study Reports (writing & reviewing documents). Responsibilities include reviewing eCRF and SAP from the medical writing perspective, reviewing Medical Coding, Data Listings and Summary results, and drafting Clinical Modules for regulatory submissions. The role also includes conducting medical writing related trainings for the project team. This position is well aligned for candidates looking for MD pharmacology jobs with exposure to late-phase studies.
Key Responsibilities:
- Authoring of Clinical Study Reports (writing & reviewing documents)
- Review of eCRF and SAP from the medical writing perspectives
- Review of Medical Coding, Data Listings and Summary results
- Drafting Clinical Modules for regulatory submissions
- Medical writing related trainings for project team
Key Deliverables:
- Clinical Study Reports of Phase II, III & IV studies
- Clinical Modules for regulatory submissions
- Regulatoy query responses
