Pharmacovigilance Specialist

4 days ago

RBangalore India Clarivate Full time ₹ 9,00,000 - ₹ 12,00,000 per year

Associate Pharmacovigilance Specialist

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.

Experience LevelMid Level

  • Principal Pharmacovigilance Specialist

    4 weeks ago

    Hyderabad, India ProPharma Full time

    Job Description For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate...

  • Data Reporting Lead

    2 weeks ago

    Noida, Uttar Pradesh, India, Ghaziabad YD Talent Solutions Full time

    Senior Data Specialist - Reporting - Pharmacovigilance (PV)Noida, IndiaOnsiteCompany Overview:Our client is a leading provider of Pharmacovigilance (PV) Technology Solutions. They bring together Life sciences domain expertise, third party system knowledge and advanced technology to develop well-defined solutions, which address challenges across PV...

  • Director of Technical Engineering

    1 week ago

    bangalore, 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,...

  • Director of Technical Engineering

    3 weeks ago

    india, IN 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,...

  • Safety Systems Specialist

    2 weeks ago

    Pune, India PrimeVigilance Full time

    Job Description Company Description We are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance,...

  • Project Manager

    3 weeks ago

    Pune, India TransPerfect Full time

    Job Description OVERVIEW: The Project Manager, Pharmacovigilance (PV) Solutions is responsible for day-to-day project management and oversight of non-linguistic PV projects, and may be in daily and regular contact with clients. This role is required to meet all client timelines and work in conjunction with fellow Project Managers, Project Coordinators,...

  • Safety Data Management Specialist

    1 week ago

    IND - Chennai Office, India Pfizer Ltd Full time ₹ 4,00,000 - ₹ 8,00,000 per year

    Associate Safety Data Management Specialist In this pharmacovigilance role, you will carry out processing activities of Individual Case Safety Reports (both clinical trials and post-marketing sources) in the ARGUS Safety database. Processing activities include assessing case validity, undertaking duplicate checks, creating cases in the database,...

  • Safety Data Management Specialist

    3 days ago

    IND - Chennai Office, India Pfizer Ltd Full time ₹ 9,00,000 - ₹ 12,00,000 per year

    Associate Safety Data Management Specialist In this pharmacovigilance role, you will carry out processing activities of Individual Case Safety Reports (both clinical trials and post-marketing sources) in the ARGUS Safety database. Processing activities include assessing case validity, undertaking duplicate checks, creating cases in the database,...

  • Safety & PV Ops Specialist I

    4 weeks ago

    Pune, India Syneos Health Full time

    Job Description Description Safety & PV Ops Specialist I Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and...

  • Associate Safety Data Management Specialist

    2 weeks ago

    Chennai, India myGwork - LGBTQ+ Business Community Full time

    Job Description This job is with Pfizer, an inclusive employer and a member of myGwork the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. In this pharmacovigilance role, you will carry out processing activities of Individual Case Safety Reports (both clinical trials and post-marketing sources) in the...