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.
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Associate Pharmacovigilance Specialist Vacancies at Clarivate, Noida[/caption]
https://pharmastuff.org.in/job/associate-pharmacovigilance-specialist-noida-careers
