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    CDM Job at Lambda | M Pharma Graduates can Apply

    CDM Job at Lambda | M Pharma Graduates can Apply

    Lambda Therapeutic Research Ltd., a global full-service Clinical Research Organization (CRO), is hiring a Technical Officer – Clinical Data Management in Ahmedabad, India. This M Pharma job in Ahmedabad is ideal for graduates looking to gain hands-on experience in clinical data management and contribute to global pharmaceutical research. Join Lambda Therapeutic and contribute to high-quality clinical research that supports innovation in the international pharmaceutical and biotech industries.

    Job Details

    • Job Position: Technical Officer – Clinical Data Management (CDM)
    • Job Location: Ahmedabad, India
    • Job ID: 1304

    About the Company

    Lambda Therapeutic Research Ltd. is a global full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India. With operations in the USA, Canada, Europe, and India, Lambda provides comprehensive end-to-end clinical research services to pharmaceutical, biotech, and generic drug companies. The company is committed to delivering high-quality, compliant, and timely clinical solutions that accelerate drug development worldwide.

    Job Description

    This role is an excellent M Pharma job opportunity for candidates with a passion for clinical data management

    • Develop eCRFs (database setup) for late-phase clinical projects.
    • Create CDM documentation such as DMP, DVP, eCCG, and other related materials.
    • Program edit checks as per data validation requirements.
    • Perform medical coding and query management activities.
    • Share CDM updates with project teams and coordinate with eDC developers.
    • Ensure compliance with data management SOPs and regulatory standards.

    Key Responsibilities

    • Set up clinical trial databases and ensure proper data validation.
    • Maintain CDM documents and ensure timely updates for project teams.
    • Conduct quality checks on clinical data for accuracy and completeness.
    • Support the clinical team in resolving queries and maintaining compliance.
    • Contribute to effective communication between project teams and data developers.

    Educational Qualification

    M.Pharm (Pharmacology)

    Experience and Skills

    • Up to 3 years of relevant experience in clinical data management or related activities.
    • Knowledge of CDM processes, clinical trial documentation, and eDC systems.

    APPLY ONLINE HERE

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