Apply for Technical Officer Report Writing job at Lambda Therapeutic Research Ltd 2026. Check eligibility, salary, and application process details here.
Introduction
The pharmaceutical and clinical research industry is continuously expanding, creating strong demand for skilled medical and report writing professionals. The Technical Officer – Report Writing Job at Lambda Therapeutic Research Ltd offers an excellent opportunity for candidates with a background in pharmacology and clinical research to build a specialized career in clinical documentation.
This role is ideal for individuals who want to work on clinical study reports and gain exposure to global regulatory standards within a reputed CRO environment.
Job Overview
| Particulars | Details |
|---|---|
| Job Title | Technical Officer – Report Writing |
| Company Name | Lambda Therapeutic Research Ltd |
| Location | Ahmedabad, India |
| Employment Type | Full-Time |
| Department | Report Writing / Clinical Research |
| Experience Required | 1–4 Years |
| Education | M.Pharm (Pharmacology) or Pharm.D |
| Salary | ₹3,50,000 – ₹6,00,000 per annum |
Company Overview
Lambda Therapeutic Research Ltd is a globally recognized Clinical Research Organization (CRO) headquartered in Ahmedabad, India. With more than two decades of experience in clinical research services, the company has established a strong presence across multiple countries including India, Poland, the UK, and the USA.
The organization specializes in providing comprehensive clinical trial solutions for biopharmaceutical and generic companies. With a workforce of over 1500 professionals, Lambda focuses on quality, innovation, and regulatory compliance to deliver reliable research outcomes.
Job Location & Employment Type
This position is based in Ahmedabad, Gujarat, and is a full-time, office-based role. Candidates should be willing to work in a collaborative clinical research environment.
Open Positions / Department Details
The vacancy is within the Report Writing team, which is responsible for preparing Clinical Study Reports (CSRs) in compliance with international regulatory guidelines. The team works closely with clinical, regulatory, and quality assurance departments to ensure accurate and high-quality documentation.
Key Roles & Responsibilities
- Prepare Clinical Study Reports (CSRs) in accordance with regulatory requirements
- Understand and apply ICH E3 guidelines in report writing
- Work on BABE (Bioavailability/Bioequivalence) study reports, especially early-phase studies
- Coordinate with cross-functional teams including QA, regulatory, and project teams
- Ensure clarity, accuracy, and compliance in all clinical documentation
- Participate in team activities such as training and quality improvement initiatives
- Manage timelines and deliver reports within project deadlines
- Maintain consistency and standardization across all reports
Eligibility Criteria
Education
- M.Pharm in Pharmacology or Pharm.D from a recognized institution
Experience
- 1 to 4 years of experience in clinical report writing or medical writing
- Experience in BABE studies or clinical trials is preferred
Skills Required
- Strong understanding of Clinical Study Report (CSR) writing
- Familiarity with ICH E3 guidelines and regulatory standards
- Good knowledge of clinical research processes
- Excellent written and verbal communication skills
- Attention to detail and strong documentation skills
- Ability to work in a team and manage multiple tasks efficiently
Salary & Benefits
- Salary Range: ₹3,50,000 – ₹6,00,000 per annum
- Opportunity to work with a global CRO
- Exposure to international clinical research standards
- Learning and development opportunities
- Collaborative and professional work environment
- Career growth in clinical and regulatory writing
Selection Process
The recruitment process generally includes:
- Initial application screening
- Technical interview focused on report writing and clinical knowledge
- HR discussion
- Final offer
How to Apply
Interested candidates can apply through the official online application portal provided by the company. Make sure your resume highlights your experience in clinical report writing and relevant regulatory knowledge.
Important Dates
- Last Date to Apply: Not specified
Why Apply for This Job?
The Technical Officer – Report Writing Job at Lambda Therapeutic Research Ltd is a great opportunity for professionals aiming to establish themselves in clinical documentation and regulatory writing.
Here’s why this role is worth considering:
- Work with a globally recognized CRO
- Gain hands-on experience in Clinical Study Reports (CSR)
- Learn international regulatory standards like ICH guidelines
- Build a strong foundation in medical writing
- Opportunity to collaborate with experienced industry professionals
This position is particularly beneficial for candidates looking to grow in medical writing, pharmacovigilance, or regulatory affairs.
FAQs
1. What is the qualification required for this job?
Candidates must have an M.Pharm (Pharmacology) or Pharm.D degree.
2. What experience is needed for this role?
A minimum of 1–4 years of experience in clinical or report writing is required.
3. What is the salary offered?
The salary ranges from ₹3.5 LPA to ₹6 LPA depending on experience and skills.
4. Is this a fresher job?
No, candidates must have at least 1 year of relevant experience.
5. What type of reports will I work on?
You will primarily work on Clinical Study Reports (CSR) related to BABE studies.
Conclusion
The Technical Officer – Report Writing Job at Lambda Therapeutic Research Ltd 2026 provides a solid career path for candidates interested in clinical research documentation. With competitive salary, global exposure, and strong learning opportunities, this role is ideal for professionals aiming to advance in medical writing and regulatory domains.
Apply soon to take advantage of this opportunity and build a rewarding career in clinical research.
Disclaimer
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