Research Associate Job at Lambda Therapeutic Research
Lambda Therapeutic Research Ltd. is hiring for the position of Research Associate at its Ahmedabad location. This opportunity is ideal for pharmacy graduates with prior experience in clinical research documentation who are looking to build a stable and progressive career in the Clinical Research Organization (CRO) industry. Research Associate Job at Lambda
The role focuses on clinical trial documentation, quality review, regulatory submissions, and ensuring compliance with standard operating procedures and global clinical research standards. Research Associate Job at Lambda
Job Details
- Job Title: Research Associate
- Requisition ID: 1483
- Company: Lambda Therapeutic Research Ltd.
- Location: Ahmedabad, Gujarat, India
- Employment Type: Full-Time
- Industry: Clinical Research / CRO
- CTC Range: ₹3,00,000 – ₹5,00,000 per annum
About the Company
Lambda Therapeutic Research Ltd. is a global, full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India. The company provides comprehensive end-to-end clinical research services to innovator, biotechnology, and generic pharmaceutical companies across the world. Research Associate Job at Lambda
With strategically located facilities in Mehsana (India), Las Vegas (USA), Toronto (Canada), Barcelona (Spain), London (UK), and Warsaw (Poland), Lambda Therapeutic Research supports clinical development programs across multiple therapeutic areas and regulatory markets. Research Associate Job at Lambda
The organization is recognized for its strong scientific expertise, robust quality systems, regulatory compliance, and commitment to ethical clinical research practices. Working at Lambda offers professionals exposure to global clinical trials, international documentation standards, and long-term career growth in the CRO domain.
Job Description
As a Research Associate, you will play a key role in supporting clinical research documentation and ensuring the quality, accuracy, and regulatory compliance of clinical trial-related documents. The position requires close coordination with cross-functional teams and adherence to documented guidelines and standard operating procedures. Research Associate Job at Lambda
The role involves reviewing, organizing, and critically analyzing scientific and clinical data to ensure that clinical trial documents accurately represent study outcomes and meet regulatory expectations.
This position is well-suited for candidates with hands-on experience in clinical documentation and a strong understanding of regulatory and quality requirements in clinical research. Research Associate Job at Lambda
Key Responsibilities
- Ensure preparation and maintenance of high-quality clinical documents that objectively and accurately represent clinical trial data
- Ensure that all deliverables are completed as per planned timelines, documented guidelines, and applicable standard operating procedures
- Assist in the supervision, planning, and review of a wide range of clinical study documents
- Work on clinical documentation including:
- Clinical CTD Modules
- Investigator’s Brochures
- Clinical Trial Protocols
- Informed Consent Forms (ICF)
- Electronic and paper Case Record Forms (CRF)
- Clinical Trial Safety Reports
- Regulatory Submission Documents
- Perform literature searches to collect and organize scientific and clinical information
- Critically examine, interpret, and summarize scientific data for clinical documentation
- Conduct quality check and review of clinical and regulatory documents to ensure accuracy, consistency, and compliance
- Support regulatory submission activities by ensuring document completeness and quality
- Maintain proper documentation and version control as per quality standards
Research Associate Job at Lambda
Skills and Competencies
- Strong understanding of clinical research documentation and regulatory requirements
- Knowledge of clinical trial processes and GCP guidelines
- Ability to perform literature searches and scientific data analysis
- Experience in reviewing and quality checking clinical and regulatory documents
- Strong attention to detail and document accuracy
- Good written communication and scientific writing skills
- Ability to interpret and summarize complex scientific information
- Time management skills with the ability to meet deadlines
- Team-oriented approach with the ability to work collaboratively
Research Associate Job at Lambda
Educational Qualifications
- B. Pharm or M. Pharm from a recognized university or institute
Experience Required
- 2 to 3 years of relevant experience in clinical research, CRO, or pharmaceutical documentation roles
Salary Details
- CTC Range: ₹3,00,000 – ₹5,00,000 per annum
- Salary will be commensurate with experience, skills, and interview performance
Research Associate Job at Lambda
Why You Should Join Lambda Therapeutic Research
- Opportunity to work with a globally recognized CRO
- Exposure to international clinical trials and regulatory documentation
- Structured work environment with strong quality and compliance systems
- Professional growth in clinical research and regulatory documentation
- Experience working with global teams and multiple regulatory regions
- Stable organization with long-term career opportunities
Research Associate Job at Lambda
FAQs
Who can apply for this Research Associate position?
Candidates with a B. Pharm or M. Pharm degree and 2–3 years of relevant clinical research experience can apply.
Is this role suitable for freshers?
No, this position requires prior experience in clinical research or documentation.
What is the job location?
The job is based in Ahmedabad, Gujarat, India.
What type of documents will I work on?
You will work on CTD modules, investigator brochures, protocols, ICFs, CRFs, safety reports, and regulatory submission documents.
What industry does this role belong to?
This role belongs to the Clinical Research Organization (CRO) and pharmaceutical research industry.
How to Apply
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Note: This job information is sourced from publicly available official sources. We share it for reference purposes only and do not claim ownership of the job posting.
