Associate Pharmacovigilance Specialist
2 days 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.).
- 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.
-
Senior Pharmacovigilance Specialist
1 week ago
Bengaluru, Karnataka, India Clarivate Full timeSenior 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...
-
PV Professional
2 weeks ago
Bengaluru, Karnataka, India beBeePharmacovigilance Full time ₹ 5,00,000 - ₹ 8,00,000PV 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...
-
Drug Safety Specialist
2 weeks ago
Bengaluru, Karnataka, India beBeePharmacovigilance Full time ₹ 1,04,000 - ₹ 1,30,878Job Title: Drug Safety AssociateJob Description:Data Retrieval: Gather and prepare data for authorizing specific sections of Periodic Safety Update Reports (PSURs).Quality Control: Review and ensure the accuracy of data retrieval processes and selected PSUR sections.PSUR Finalization: Finalize PSURs, including creating the final PSUR PDFs.Regulatory...
-
Compliance Expertise
2 weeks ago
Bengaluru, Karnataka, India beBeeRisk Full time ₹ 15,00,000 - ₹ 28,00,000Job Title: Risk and Compliance Specialist We are seeking a highly skilled Risk and Compliance Specialist to join our team. In this role, you will be responsible for ensuring that our company adheres to all relevant laws and regulations.Key Responsibilities: Conduct risk assessments to identify potential compliance issues. Ensure...
-
Associate Document Specialist
1 week ago
Bengaluru, Karnataka, India Cloudxtreme Full time ₹ 5,00,000 - ₹ 8,00,000 per yearAssociate Docs to Stips SpecialistDigital Risks mission to Make Mortgages Safe relies on the perfect blending of human experience and state-of-the-art technology to serve its workforce and clients. Digital Risk's 1,500+ team members make us one of the largest mortgage outsource providers in the U.S., supplying appraisal and mortgage processing, underwriting,...
-
Bengaluru, Karnataka, India CSC Full time ₹ 1,04,000 - ₹ 1,30,878 per yearAssociate Client Onboarding SpecialistLocation: BangaloreDepartment: Fund ServicesVacancy Type: PermanentWork Timings: APACWork Mode: HybridThe position:As an Associate Client Onboarding Specialist, you will be responsible for ensuring a smooth onboarding experience for new clients and the ongoing account maintenance. You will work closely with various Fund...
-
Associate Medical Reviewer
3 weeks ago
Bengaluru, Karnataka, India Novo Nordisk Full timeBy continuing to use and navigate this website you are agreeing to the use of cookies Accept Close Press Tab to Move to Skip to Content Link Search by Keyword Search by Location Loading Category Select how often in days to receive an alert x Select how often in days to receive an alert Associate Medical Reviewer Category Clinical...
-
Safety Data Analyst
2 weeks ago
Bengaluru, Karnataka, India beBeePharmacovigilance Full time ₹ 1,04,000 - ₹ 1,30,878Job SummaryWe are seeking a skilled professional to join our team as a Pharmacovigilance Associate.The successful candidate will be responsible for retrieving and preparing data for authoring selected Periodic Safety Update Reports (PSURs), reviewing and performing quality control on the data retrieval procedures and selected PSUR sections, finalizing PSURs...
-
Physician Medical Safety Specialist
2 weeks ago
Bengaluru, Karnataka, India beBeeMedicalReviewer Full time ₹ 13,51,897 - ₹ 16,22,273Medical Reviewer Job Description:As a medical reviewer, you will be responsible for the comprehensive review of individual case safety reports (ICSRs) and ensuring compliance with regulatory requirements.Perform medical review of ICSRs for accuracy, medical relevance, and consistency with source documents and safety database entries, in alignment with client...
-
Associate Product Specialist
2 hours ago
Bengaluru, Karnataka, India Informatica Full time ₹ 8,00,000 - ₹ 12,00,000 per yearBuild Your Career at InformaticaWe seek innovative thinkers who believe in the power of data to drive meaningful change. At Informatica, we welcome adventurous, work-from-anywhere minds eager to tackle the world's most complex challenges. Our employees are empowered to push their bold ideas forward, and we are united by a shared passion for using data to do...