Associate Pharmacovigilance Specialist Vacancies at Clarivate, Noida

Associate Pharmacovigilance Specialist Vacancies at Clarivate, Noida
    • Full Time
    • Noida
    • ₹30000 INR / Month

    Associate Pharmacovigilance Specialist Vacancies in Noida – Your Gateway to a Rewarding Career

    Are you a skilled professional in Life Sciences or Biomedical Sciences? Are you passionate about drug safety and ensuring the well-being of patients? Look no further – our client, Clarivate, seeks talented individuals to join their dynamic team as Associate Pharmacovigilance Specialists in Noida. Dive into a fulfilling role where your expertise in biomedical literature monitoring and adverse event reporting will significantly impact you.

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    About Clarivate:

    Clarivate is a global leader in providing pharmacovigilance services across various therapeutic areas. Committed to excellence, Clarivate offers a supportive working environment with personalized training opportunities for professional growth. Join a team dedicated to maintaining the highest drug safety and customer engagement standards.

    Company Vacancies:

    Explore the exciting career opportunities at Clarivate. Here’s a snapshot of tHere’silable positions:

    • Position Title: Associate Pharmacovigilance Specialist
    • Company Name: Clarivate
    • Salary: Competitive
    • Company Address: Noida, UP
    • Detailed Job Description: (Detailed job description provided below)
    • Role: Drug Safety
    • Industry Type: Pharma
    • Department: Pharmacovigilance
    • Employment Type: Full Time
    • Role Category: Medical/Healthcare
    • Educational Background Required: Master’s Degree in LifMaster’ses, Health, or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, etc.)
    • Key Skills: Biomedical Literature Monitoring, Adverse Event Reporting, Writing Skills

    Duties and Responsibilities:

    • Critically analyses large numbers of articles from biomedical published literature and internal drug safety alerts and identifies individual case safety reports (ICSRs) as well as other potential safety-relevant information impacting the risk-benefit and/or safety profile of customer’s products, acustomer’sicable regulatory requirements and standard operating procedures.
    • Write brief narratives summarizing summarising and other potentially safety-relevant information in each article.
    • Demonstrates understanding of clients’ drug labels and effectively performs safety assessments.
    • Completes drug safety reviewing of each biomedical literature batch in a timely, thorough, and accurate manner in accordance with the client’s standards of client’s quality.
    • Uses a drug safety system to track all actions and assessments in an audit-ready reference history.
    • Select articles specific to the client’s interest for clients in the client’s product literature per guidelines.
    • Writes accurate, detailed, and complete abstracts of selected articles using good judgement regarding the level of detail required and excellent organization and grammar.
    • Extracts key points organisation and creates comprehensive and detailed indexes of the abstract contents to ensure precise and complete literature retrieval from the client’s database.
    • Client timely completion of indexing and abstracting of articles for assigned drugs by regulatory submission deadlines.
    • Maintains an awareness of new drugs and therapeutic categories, new disease entities, and changes in biomedical terminology in the published literature.
    • Participates in other duties such as searches and terminology maintenance according to business needs and the training provided.

    Educational Qualifications:

    • Master’s Degree in LifMaster’s, Health, or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics etc.).
    • A degree in Dentistry, physiotherapy, or nursing, which involves patient exposure in a hospital-based environment, would be an advantage.
    • At least 1-2 years of experience reviewing biomedical literature for adverse event reporting.
      • OR equivalent combination of education and experience (i.e., an information science degree with at least 1 year of relevant working knowledge of supporting drug and patient safety)
    • Related experience in drug safety/ pharmacovigilance is desirable.
    • Strong analytic ability to analyse and summarize biomedianalyzee reports, studies, or topics.
    • At least 1 year of experience using writing skills to support the creation of succinct, accurate, and precise summaries.
    • At least 1 year of working knowledge of biomedical terminology, drugs, and therapeutic areas

    Ancillary Qualifications:

    Qualifications listed below, while not necessarily a requirement for this position in each circumstance,

    provide additional depth and value to the role.

    • Certification from a professional medical writer’s association
    • Ewriter’se with commercial and client-specific biomedical literature databases
    • Scientific/medical writing background

    Skills:

    • Excellent English language skills (comprehension, speaking, reading, and writing).
    • Working knowledge of biomedical terminology, drugs, and therapeutic areas.
    • Experience with commercial and client-specific biomedical literature databases.
    • Flexibility and adaptability to changing client needs.
    • Ability to work effectively, independently, and collaboratively.

    About the Department & Responsibilities:

    Join the pharmacovigilance team at Clarivate, providing services across therapeutic areas. Engage in a supportive working environment and receive personalized training on ppersonalizedance and customer engagement.

    How to Apply:

    Ready to embark on this exciting career journey? Visit our careers page to apply for the Associate Pharmacovigilance Specialist position in Noida.

    Hours of Work:

    The team operates from 11:00 AM IST to 8:00 PM IST Monday through Friday, with a hybrid work mode. Candidates are required to work from the office at least two to three days a week.

    • Fraud Warning: Please be advised that there have recently been fraudulent job offers and interviews using the Clarivate name, logo, and even the names of our colleagues.
    Associate Pharmacovigilance Specialist Vacancies at Clarivate, Noida
    Associate Pharmacovigilance Specialist Vacancies at Clarivate, Noida

    To apply for this job please visit careers.clarivate.com.

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