▷ [Apply Now] Associate Pharmacovigilance Specialist
4 weeks ago
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 Fresher Upto 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 Working knowledge of biomedical terminology drugs and therapeutic areas Experience with commercial and client-specific biomedical literature databases 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 A degree in Dentistry physiotherapy Nursing which involves patient exposure in hospital-based environment would be an advantage Work hours Monday to Friday Hybrid work model 12PM - 9 PM 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
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Noida, India Clarivate Full timeJob Description 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 -...
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Associate Pharmacovigilance Specialist-7
5 days ago
Noida, Uttar Pradesh, India Clarivate Full time ₹ 6,00,000 - ₹ 18,00,000 per yearJob Responsibilities:Under supervision, evaluate literature reports for potential cases of adverse events or safety concerns requiring further investigation and escalate case processing and follow-up.Extract pertinent safety data from identified literature sources, including adverse events, safety signals, and other relevant information, ensuring accuracy...
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Noida, India YD Talent Solutions Full timeDescription : Senior Data Specialist Reporting Pharmacovigilance (PV). Noida, India. Onsite. Company 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...
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Associate Business Analyst
2 weeks ago
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Noida, Uttar Pradesh, India Wipro Full timeWe use cookies to offer you the best possible website experience Your cookie preferences will be stored in your browser s local storage This includes cookies necessary for the website s operation Additionally you can freely decide and change any time whether you accept cookies or choose to opt out of cookies to improve website s performance as well as...