Job Title: Technical Officer – Clinical Research
Location: Ahmedabad, India
Employment Type: Full-Time
CTC Range: INR 3,00,000 – 5,00,000
Experience Required: Up to 2 years in clinical research or clinical data management
Company Overview:
Lambda Therapeutic Research Ltd. is a leading full-service Global Clinical Research Organization (CRO) headquartered in Ahmedabad, India. With strategic operations in Mehsana (India), Las Vegas (USA), Toronto (Canada), Barcelona (Spain), London (UK), and Warsaw (Poland), Lambda delivers comprehensive end-to-end clinical research services to innovator, biotech, and generic pharmaceutical companies worldwide.
Role Overview:
We are seeking a Technical Officer to support our Clinical Data Management (CDM) and late-phase clinical trial activities. The ideal candidate will have hands-on experience in eDC platforms, clinical data validation, and query management, with the ability to contribute to study planning, execution, and close-out processes.
Key Responsibilities:
Design, develop, test, and update electronic Case Report Forms (eCRFs) for clinical trials.
Perform clinical data validation, data cleaning, and query management.
Conduct medical coding for concomitant medication data captured in the electronic data capture (eDC) system.
Maintain and update CDM documentation, including SOPs, validation reports, and training materials.
Support late-phase clinical trial activities, including planning, execution, and close-out processes.
Collaborate with cross-functional teams to ensure high-quality, accurate, and compliant clinical data management.
Participate in training sessions and knowledge sharing for team members on CDM practices and tools.
Required Qualifications:
Bachelor’s or Master’s degree in Life Sciences, Clinical Research, Pharmacy, or Medical Sciences (BDS, BHMS, BAMS, M.Pharm, M.Sc. Life Sciences/Clinical Research).
Up to 2 years of experience as a Clinical Research Coordinator (CRC) or within a Clinical Data Management team.
Hands-on experience with eDC platforms, data validation, and query management.
Familiarity with clinical trial processes and late-phase study operations.
Preferred Skills:
Knowledge of medical coding standards and clinical data quality processes.
Strong analytical and problem-solving skills.
Effective verbal and written communication skills.
Ability to work collaboratively within a fast-paced, matrixed environment.
Attention to detail and commitment to regulatory compliance and data integrity.
Why Join Lambda Therapeutic Research:
Gain exposure to global clinical trials across multiple therapeutic areas.
Work with an experienced team on cutting-edge clinical research projects.
Develop expertise in Clinical Data Management and late-phase trial operations.
Opportunity to grow your career in a global, fast-growing CRO.
Apply Now:
Advance your career in clinical research with Lambda Therapeutic Research, contributing to high-quality studies that impact patient outcomes worldwide.
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