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    Freshers Job Alert | Regulatory Affairs Position at ClinChoice | Pharma Graduates Apply Now

    Freshers Job Alert | Regulatory Affairs Position at ClinChoice | Pharma Graduates Apply Now

    ClinChoice is hiring an Associate – Regulatory Affairs for its RegPoint team in Bengaluru, India. This full-time, permanent office-based Regulatory Affairs Position is designed for B.Pharm or M.Pharm freshers (0–1 year experience). The successful candidate will manage RIMS data clean-up, support business users, and process submission intake requests, ensuring global regulatory compliance through high-precision data management.

    • Job Title: Associate – Regulatory Affairs (RegPoint)
    • Location: Bengaluru, India

    About The Company

    ClinChoice is a partner to the largest pharmaceutical, medical device, and consumer care innovators in the world. Established in 1995, we provide expertise in clinical operations, biometrics, regulatory affairs, pharmacovigilance, medical affairs, and toxicology to help our partners advance healthcare by accelerating clinical trials with data-driven insights, delivering the best strategies for product registration, and enhancing patient safety through real-world and clinical analysis.

    Primary Responsibilities

    • Perform required data clean-up as per the defined process in the Regulatory Information Management System (RIMS).
    • Support business users by reviewing the data entered into the RIMS application and providing updates to users.
    • Complete assigned user requests on a daily basis as per the defined process.
    • Communicate with business users regarding queries related to user requests.
    • Process submission intake requests and ticket requests.

    Secondary Responsibilities

    • Collect information from different sources and locations (manual and electronic), including supporting reports.
    • Enter collected information manually into RIMS for storage and analysis.
    • Perform peer quality checks of data entered against source documents.

    Job Requirements

    • Fresher or candidates with 3–6 months of experience in RIMS regulatory data management are preferred.
    • B.Pharm or M.Pharm qualification.
    • Proficiency in computer software and systems such as MS Office; exposure to Regulatory Information Management System (RIMS) software and document management tools is an added advantage.
    • Excellent communication skills in English, both written and verbal.

    LINK TO APPLY ONLINE

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