Associate Pharmacovigilance Specialist Vacancies at Clarivate, Noida

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

Are you a skilled professional in the field of Life Sciences or Biomedical Sciences? Are you passionate about drug safety and ensuring the well-being of patients? Look no further – our client, Clarivate, is seeking 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 make a significant impact.

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 and diverse opportunities for professional growth. Join a team dedicated to maintaining the highest standards of drug safety and customer engagement.

Company Vacancies:

Explore the exciting career opportunities at Clarivate. Here’s a snapshot of the available 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 Life Sciences, 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, as per applicable regulatory requirements and standard operating procedures.
• Write brief narratives summarizing the ICSR criteria and other potentially safety-relevant information in each article.
• Demonstrates understanding of client’s drug labels and uses that knowledge effectively when performing the safety assessments.
• Completes drug safety reviewing of each biomedical literature batch in a timely, thorough, and accurate manner in accordance with client’s standards of timeliness and quality.
• Uses drug safety system to track all actions and assessments in an audit-ready reference history.
• Selects articles specific to client’s interest for inclusion in client’s product literature database per guidelines.
• Writes accurate, detailed, and complete abstracts of selected articles using good judgement regarding the level of detail required and excellent organization, grammar, and syntax.
• Extracts key points of articles and creates comprehensive and detailed indexes of the abstract contents to ensure precise and complete retrieval of literature from client’s database.
• Ensures timely completion of indexing and abstracting of articles for assigned drugs in accordance with regulatory submission deadlines.
• Maintains an awareness of new drugs and new 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 per the training provided.

Educational Qualifications:

• 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

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
• Experience 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, receive personalized training, and contribute to various aspects of pharmacovigilance 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-Friday, with a hybrid work mode. Candidates are required to work from the office at least 2 to 3 days a week.

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