Clinical Research Job at Lambda Therapeutic Research | Apply
Looking for a rewarding clinical research job in Ahmedabad? Lambda Therapeutic Research Ltd., a leading global Clinical Research Organization (CRO), is offering an excellent opportunity for aspiring professionals through its Technical Officer job opening. Join a world-class research environment and gain hands-on experience in Clinical Data Management, working with international teams across global projects.
Job Details:
- Job Position: Technical Officer
- Job ID: Req ID: 1439
- Location: Ahmedabad, India
- CTC Range (INR): ₹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. Recognized for excellence in clinical trial management, Lambda operates in Mehsana (India), Las Vegas (USA), Toronto (Canada), Barcelona (Spain), London (UK), and Warsaw (Poland). The company provides end-to-end clinical research services for innovator, biotech, and generic pharmaceutical industries, making it a preferred destination for professionals pursuing clinical research jobs in Ahmedabad.
Clinical Research Job – Qualifications:
- Educational Qualification: BDS, BHMS, BAMS
- Experience: Up to 2 years of experience as a Clinical Research Coordinator (CRC) or as a Data Manager/Data Validator in a CDM department.
- Desired Skills: Understanding of eDC platforms, strong analytical mindset, and familiarity with clinical trial workflows.
Job Description:
This Technical Officer job at Lambda Therapeutic Research offers a chance to be part of impactful clinical research projects. The role involves Clinical Data Management (CDM) responsibilities across various stages of late-phase clinical trials – from planning to close-out. The ideal candidate will work on eCRF design, data validation, query management, and medical coding, ensuring data accuracy and compliance with regulatory standards.
Clinical Research Job – Key Responsibilities:
- Manage Clinical Data Management activities, including eCRF designing, data validation, query management, and training coordination.
- Participate actively in late-phase clinical trials – planning, execution, and close-out.
- Conduct medical coding for concomitant medication data captured in electronic data capture (eDC) systems.
- Perform eCRF development, testing, and updates as per study requirements.
- Maintain CDM documentation in accordance with quality and compliance standards.
