Associate Pharmacovigilance Specialist

1 week ago


Bengaluru, India Clarivate Full time

The Associate pharmacovigilance specialist performs pharmacovigilance services such as biomedical literature monitoring and assessing for adverse events reporting, indexing, and abstracting by using broad knowledge of scientific terms and medical terminology, drugs and therapeutic areas, and pharmacovigilance regulations.

About You - Education, Experience, Skills

  • Master's Degree in life Sciences, Health, or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics etc.).
  • A degree in Dentistry/physiotherapy/Nursing, which involves patient exposure in 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 the main points of biomedical case reports, studies, or specific 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
  • 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.
  • Basic computer literacy.

It would be great if you also had . . .

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

Work hours

Monday to Friday - Hybrid work mode

The preceding job description is not intended to describe in detail the multitude of tasks that may be assigned, but rather to provide a general overview of the expectations and responsibilities of this position. As the nature of business demands change, so may the functions of this position. Additional duties and responsibilities may be assigned.

At Clarivate, we are committed to providing equal employment opportunities for all qualified persons with respect to hiring, compensation, promotion, training, and other terms, conditions, and privileges of employment. We comply with applicable laws and regulations governing non-discrimination in all locations.



  • Bengaluru, Karnataka, India Clarivate Full time ₹ 9,00,000 - ₹ 12,00,000 per year

    The Associate pharmacovigilance specialist performs pharmacovigilance services such as biomedical literature monitoring and assessing for adverse events reporting, indexing, and abstracting by using broad knowledge of scientific terms and medical terminology, drugs and therapeutic areas, and pharmacovigilance regulations.About You - Education, Experience,...


  • Bengaluru, India Bitwise Solutions Full time

    Job description WHO defines Pharmacovigilance (PV) as the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other drug-related problem. Pharmacovigilance is also known as drug safety and it focuses on ADR (Adverse drug reaction).The main aim of Pharmacovigilance is to monitor approved drugs...


  • Bengaluru, Karnataka, India Entirety Hr Solutions Full time ₹ 9,00,000 - ₹ 12,00,000 per year

    Job Role: Senior Pharmacovigilance AssociateProcessing of the Individual Case Safety Reports (ICSR).Literature screening activities.Accountable for reviewing and assessing the validity of literature abstracts and articles with further processing onto the safety database if required.Extended Eudravigilance Medical Product Dictionary (XEVMPD) maintenance and...


  • Bengaluru, Karnataka, India Clarivate Full time

    Senior Pharmacovigilance SpecialistJob Profile SummaryThis position involves Biomedical Literature Searching in our team and requires knowledge of biomedical literature and searching databases such as MEDLINE Embase and Biosis Previews You will need broad knowledge of biomedical terminology drugs and therapeutic areas In this role you are responsible...


  • Bengaluru, India Ardent Research Full time

    **KEY ACCOUNTABILITIES** - Responsible for monitoring and management of departmental documents, quality, workload and resource allocation. - Ensure timely escalation of issues and concerns to the Head of Pharmacovigilance. - Provide support to the Head of Pharmacovigilance and assist with review of proposals, costings for PV business and bid defense...

  • PV Professional

    2 weeks ago


    Bengaluru, Karnataka, India beBeePharmacovigilance Full time ₹ 5,00,000 - ₹ 8,00,000

    PV Specialist Role We are seeking a skilled PV Specialist to join our team. As a key member, you will play a pivotal role in ensuring the high-quality execution of pharmacovigilance processes. Key Responsibilities: Literature Review: Design and implement comprehensive search strategies using databases such as Embase, Medline, PubMed, and Ovid to ensure...


  • Bengaluru, India Qinecsa Solutions Full time

    About the CompanyQinecsa is a trusted, global partners bringing together best-in-class technology and scientific expertise to connect life science companies, public health, and regulatory sectors to the right safety solutions. we take pride in being the leading specialist pharmacovigilance provider, offering unparalleled expertise in PV services, technology,...


  • Bengaluru, India Novaspire Biosciences Full time

    Company Description Novaspire Biosciences Private Limited is a healthcare company specializing in Pharmacovigilance, Clinical Research, and Bioavailability/Bioequivalence studies Project Management support. Novaspire is dedicated to enhancing patient safety and promoting public health through innovative solutions for the pharmaceutical and biotechnology...


  • Bengaluru, India Nes Global Specialist Engineering Services Full time

    Invoicing Associate Location: Bangalore "Join our growing team as an Invoicing Associate where accuracy counts ABOUT THE ROLE: As an Invoicing Associate, you will play a key role in maintaining the financial accuracy of our operations by ensuring timely and precise invoicing. You will be responsible for preparing and issuing invoices to customer and meet the...


  • Bengaluru, Karnataka, India Indegene Full time

    **Date**:22 Aug 2025 **Location**:Bangalore, KA, IN - Job Description- - Must Have- Associate - Pharmacovigilance Officer I You will be responsible for: "Confirm validity of case by identifying minimum criteria for case creation. - Perform duplicate search to create either an initial case or a follow-up case. - Understanding the principles and concepts...