Drug Safety Physician (mbbs, MD)-Chandigarh

Company:Kelly Services India Pvt. Ltd. hiring for CRO in Chandigarh

Location:Chandigarh

Experience : 0 - 5 yrs

Salary: 7,00,000 - 13,00,000 P.A

Industry: Pharma / Biotech / Clinical Research

Functional Area: Medical , Healthcare , R&D , Pharmaceuticals , Biotechnology

Role Category:Medical Professional

Role:Clinical Researcher



Key Skills : MBBS Pharmacovigilance MD PSUR ICSR Clinical Study Clinical Research Clinical Monitoring Pharma and Clinical Research drug safety

Job Description
    Education:

    UG: MBBS - Medicine

    PG:Post Graduation Not Required, M.S/M.D - Any Specialization

    Doctorate: Doctorate Not Required

    **Ayurvedic, homeopathic, veterinary doctors or from other alternative medical streams and scientists with life sciences background need not apply for this position; A degree in Medicine (MBBS) or a post-graduation qualification (MD) is desired .

    Fluency in written and spoken English is must

    Job Description

    Report preparation [e.g. Periodic Safety Update Reports (PSURs), Addendum PSURs, Bridging Reports, PSUR Line Listings, US PADERs] from aggregate data for products, in accordance with client conventions and requirements;

    Quality checks of aggregate reports; Signal detection-related analyses and reports including cumulative analyses, issue event analyses, Drug Safety Reports , review of published literature and case listings; Vigilance over important/designated medical events;

    Interaction with client personnel to discuss potential signals and issues detected with products; Support preparation and maintenance of Risk Management Plans;

    Follow-up and interaction with clients to obtain incomplete/missing information, with a view to resolving and clarifying issues;

    Performing medical review of individual case safety reports (ICSRs); Performing medical review of narratives for Clinical Study Reports (CSRs);

    Providing medical advice to drug safety scientists to assist them with processing of ICSRs and CSR narratives;

    Maintaining an excellent knowledge of the adverse event safety profile of assigned drugs, labelling documents, and client guidelines and Standard Operating Procedures (SOPs);

    Maintaining an awareness of global regulatory reporting obligations and organizing workload to ensure compliance with internal and regulatory timelines for report submissions;

    Maintaining records in compliance with guidelines and SOPs