Lambda CRO Hiring: Manager – Report Writing Role Opens Doors for MD Pharmacology Talent in Ahmedabad
Lambda CRO Hiring is underway for an exciting entry-level management position in the heart of India’s pharmaceutical hub! Lambda Therapeutic Research Limited, a leading global full-service Contract Research Organization (CRO), is seeking highly motivated MD Pharmacology freshers for the role of Manager – Report Writing in Ahmedabad.
This opportunity is perfect for recent graduates looking to blend scientific rigor with technical writing, making a direct impact on regulatory success and drug development. If you are ready for a fast-paced career in clinical research, this is your moment.
Meet Lambda Therapeutic Research (Background Context)
Founded in 1999, Lambda Therapeutic Research Limited is a powerhouse in accelerating drug development globally. With over two decades of expertise, Lambda has supported over 275 clinical trials across 15+ therapeutic areas, focusing heavily on biosimilars and early-to-late phase studies.
Global Reach: Headquartered in Ahmedabad, Lambda operates across India, USA, Canada, UK, Spain, and Poland.
Expansion: The 2019 acquisition of Novum Pharmaceutical Research Services significantly boosted its North American footprint.
Excellence: The company is a recognized leader in PK/PD studies, bioanalytical services, and medical writing, holding awards like the 2023 CPHI Regulatory Excellence Award.
Joining Lambda means stepping into a culture of integrity, growth, and global influence, supported by over 1,000 professionals.
The Manager – Report Writing Opportunity
This position is designed for individuals seeking rapid professional development in the crucial field of Medical Writing within Clinical Research.
| Detail | Requirement |
| Company Name | Lambda Therapeutic Research Limited |
| Department | Clinical Research / Medical Writing |
| Role | Manager – Report Writing |
| Qualification | MD Pharmacology (Mandatory) |
| Experience | Fresher to 1 year |
| Location | Ahmedabad, Gujarat (On-site) |
Note: Although titled “Manager,” this role is explicitly framed for entry-level candidates, making it an excellent launching pad for a career in regulatory and clinical documentation.
Key Responsibilities and Required Skills
The core function of this role is to transform clinical trial data into clear, regulatory-compliant narratives that support market access for new therapies.
Key Responsibilities
Drafting CSRs: Draft and edit Clinical Study Reports (CSRs) in compliance with global regulatory and ICH-GCP guidelines.
Research: Perform comprehensive literature searches essential for protocol development and scientific documentation (e.g., using PubMed, Embase).
Regulatory Support: Collaborate with cross-functional teams on regulatory submissions and manage query responses from health authorities.
Compliance: Review scientific documents for accuracy and ensure the team adheres to established quality standards and SOPs.
Essential Skills & Qualifications
Strong foundational knowledge in pharmacology and clinical trial methodologies.
Familiarity with medical writing principles and the CSR development process.
Excellent English communication skills (written and verbal) for technical documentation.
An analytical mindset for efficient data interpretation and synthesis.
Why Start Your Career with Lambda CRO
Lambda offers a highly supportive environment where fresh talent is nurtured into industry leaders.
Accelerated Growth: Benefit from rapid career progression and hands-on learning through mentorship and exposure to multi-country operations.
Global Exposure: Work on innovative biosimilar and generic drug programs with a firm operating in six countries.
Compensation: Receive a competitive salary package paired with performance bonuses.
Stability: Enjoy long-term stability in a firm recognized for over 20% annual growth and continuous strategic expansion.
How to Apply
Don’t miss this chance to join a legacy of excellence in clinical research.
Visit the dedicated career portal: careers.lambda-cro.com.
Submit your updated resume and a cover letter that specifically highlights your MD Pharmacology background and keen interest in Medical Writing.
Authoritative Source: This job posting is verified and available on the Lambda Research Accelerated LinkedIn page.
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Lambda Research Accelerated LinkedIn page.
