PV Safety Specialist III vacancies at Thermo Fisher Scientific | Apply Now

Thermo Fisher Hyderabad Hiring PV Safety Specialist III
    • Full Time
    • Hyderabad
    • 55000 INR / Month

    Join Thermo Fisher Scientific as a PV Safety Specialist III in Hyderabad

    Thermo Fisher Scientific is seeking a PV Safety Specialist III to join our Pharmacovigilance (PVG) team in Hyderabad, Andhra Pradesh, India. In this role, you will be responsible for performing and overseeing day-to-day PVG activities within a highly regulated environment. Your work will be driven by strict timelines and will involve collection, monitoring, assessment, evaluation, research, and tracking of safety information related to pharmaceutical products.

    Key responsibilities:

    • Works independently to perform day-to-day PV activities. May participate in on call duties for specific projects to ensure 24-hr coverage for intake of cases from investigative sites.
    • Operates in a lead capacity. Provides assistance in the development of program and departmental procedural documents. May prepare for and attend audits. Mentors less expert staff. Reviews regulatory/pharmacovigilance publications and information sources t
    • keep updated on current regulations, practices, procedures and proposals. Maintains medical understanding of applicable therapeutic area and disease states. Reviews cases entered for quality, consistency and accuracy, including review of peer reports.
    • Responsible for routine project implementation and coordination (e.g., Clinical Trials, Endpoint Assessment Committee/Data Safety Monitoring Committee), including presentations at client/investigator meetings, and review of metrics and budget considerations.
    Thermo Fisher Hyderabad Hiring  PV Safety Specialist III
    Thermo Fisher Hyderabad Hiring PV Safety Specialist III

    Qualifications:

    • Bachelor’s degree or equivalent with at least 5+ years of relevant experience in pharmacovigilance or a related field.
    • Thorough understanding of pathophysiology and disease processes.
    • Strong knowledge of relevant therapeutic areas for processing adverse events (AEs).
    • Excellent critical thinking, problem-solving, and communication skills.
    • Proficiency in clinical study administration, budget activities, and Microsoft Office products.
    • Familiarity with global regulatory requirements and compliance with procedural documents and regulations.
    • Ability to work independently, prioritize tasks, meet strict deadlines, and maintain professionalism under stress.

    Join Our Team:

    At Thermo Fisher Scientific, you’ll be part of a global team dedicated to making the world healthier, cleaner, and safer. We offer opportunities for career growth, professional development, and meaningful work that impacts lives worldwide.

    Apply today to start your journey with us at Thermo Fisher Scientific Careers

    Thermo Fisher Scientific is an Equal Opportunity Employer and values diversity in the workplace.

    To apply for this job please visit jobs.thermofisher.com.

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