Job Title: Technical Officer – Clinical Data Coordinator
Job Category: Clinical Research / Clinical Data Management (CDM) / Data Operations
Job Type: Full-Time
Location: Ahmedabad, Gujarat, India
Req ID: 1540
CTC Range: INR 3,00,000 – 6,00,000 per annum
Company Overview
Lambda Therapeutic Research Ltd. is a global full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India. The organization delivers end-to-end clinical research solutions to innovator, biotechnology, and generic pharmaceutical companies worldwide.
With a strong international presence across India, North America, and Europe, Lambda operates under globally compliant regulatory standards, ensuring data integrity, subject safety, and operational excellence across all clinical development programs.
Role Overview
We are seeking a Technical Officer – Clinical Data Coordinator to support clinical data management activities for late-phase clinical trials. The ideal candidate will have hands-on experience at the site level as a Clinical Research Coordinator (CRC) and strong exposure to electronic data capture systems, data validation processes, and clinical documentation standards.
This role plays a critical part in ensuring accurate, complete, and regulatory-compliant clinical trial data across global studies.
Key Responsibilities
Design, develop, and test electronic Case Report Forms (eCRFs) in alignment with study protocols and data management plans.
Perform data validation, discrepancy management, and query resolution to maintain high-quality clinical datasets.
Prepare and maintain Clinical Data Management documentation including Data Management Plans (DMP), Data Validation Plans (DVP), and eCRF Completion Guidelines (eCCG).
Conduct data reconciliation activities with external vendors and internal stakeholders.
Perform medical coding using standard dictionaries (e.g., MedDRA, WHO-DD).
Support user training for EDC systems and related clinical data platforms.
Collaborate with cross-functional teams to ensure timely database lock and regulatory submission readiness.
Required Experience
Relevant experience working at the site level as a Clinical Research Coordinator (CRC) in late-phase clinical trials.
Hands-on experience with Electronic Data Capture (EDC) systems and related platforms such as IWRS and ePRO.
Practical exposure to clinical data management activities including query management and database review.
Strong understanding of ICH-GCP guidelines and clinical trial documentation standards.
Good analytical skills and attention to detail in handling clinical datasets.
Educational Qualification
M. Pharm (Pharmacology or Quality Assurance), or
BDS / BAMS / BHMS, or
M.Sc. in Life Sciences or related discipline.
Professionals with experience in clinical data coordination and late-phase trial management are encouraged to apply through ThePharmaDaily.com for confidential consideration.
Uttar Pradesh :
Agra | Gajraula | Gautam buddha Nagar | Ghaziabad | Gorakhpur | Greater Noida | Jhansi | kanpur | Lucknow | Mathura | Noida | Park City | Prayagraj | Satyamev | Varanasi |Gujarat :
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