Are you passionate about advancing medical science and ensuring the success of clinical trials? Lambda Therapeutic Research Ltd., a leading global Clinical Research Organization (CRO), is seeking a dedicated Clinical Research Associate I to join their team in Ahmedabad, India. With a reputation for excellence in clinical research services, Lambda offers an exciting opportunity for professionals to contribute to cutting-edge pharmaceutical research. This role is ideal for candidates with a medical science background looking to make an impact in late-phase clinical trial operations.
About Lambda Therapeutic Research Ltd.
Lambda Therapeutic Research is a full-service CRO headquartered in Ahmedabad, India, with operations in Mehsana (India), Las Vegas (USA), Pittsburgh (USA), Toronto (Canada), Warsaw (Poland), and London (UK). The company provides comprehensive clinical research services to global innovator, biotech, and generic pharmaceutical industries, ensuring high-quality trial execution and compliance with international standards.
Job Responsibilities
As a Clinical Research Associate I in late-phase clinical trial operations, you will play a pivotal role in ensuring the smooth execution of clinical studies. Key responsibilities include:
- Training Site Staff: Provide training on study protocols and related documents to ensure site readiness.
- Conducting Site Visits: Perform Study Site Visits (SSV), Site Initiation Visits (SIV), Site Monitoring Visits (SMV), and Site Close-Out Visits (SCOV) as per project scope.
- Managing Study Sites: Maintain close coordination with study sites for patient screening, recruitment, and follow-up activities.
- Ensuring Compliance: Verify adherence to study protocols, regulatory requirements, and proper documentation at study sites.
- Study Material Management: Ensure timely availability of study materials and Investigational Medicinal Products (IMP).
- Communication Liaison: Act as the primary communication link between Lambda’s team and study sites.
- Data Review: Review source data at study sites to ensure accuracy and compliance.
- Site Master File (SMF) Updates: Maintain and update the SMF to reflect current study status.
Qualifications and Experience
To excel in this role, candidates should meet the following requirements:
- Educational Background: M. Pharm, B. Pharm, M. Sc., B. Sc., BAMS, BHMS, Dentist, or equivalent qualification in medical sciences.
- Experience: Minimum 5 years in the pharmaceutical industry, with at least 1 year as a Clinical Research Associate (CRA) in clinical trials.
- Skills: Strong organizational skills, attention to detail, and knowledge of clinical trial regulations (e.g., ICH-GCP).
- Communication: Excellent interpersonal and communication skills to liaise with study sites and internal teams.
Benefits of Joining Lambda Therapeutic Research
- Competitive Salary: CTC range of INR 5,00,000–8,00,000 per annum.
- Global Exposure: Work with a globally recognized CRO serving innovator and generic pharmaceutical industries.
- Career Growth: Opportunities for professional development in clinical research and trial management.
- Collaborative Environment: Join a dynamic team dedicated to advancing medical science.
How to Apply
