Pharmacovigilance Associate
1 month ago
recording and reporting adverse reactions received from healthcare professionals and consumers
- conducting in-depth interviews with patients and healthcare professionals
- developing a thorough knowledge of products
- completing periodic safety update reports on drugs and other treatments
- writing and reviewing serious adverse effects reports and forms
- flagging up early warning signs of adverse effects of drugs
- minimising the risk of serious side effects
- completing safety audits
- working on clinical trials of new drugs
- Ability to keep meticulous records
- Attention to detail
- Excellent analytical and problem-solving skills
- Ability to interact and communicate effectively with a wide range of people
- A systematic approach to tasks
- Excellent IT skills
- Good interpretative skills
- Team work
- Good maths skills
**Salary**: ₹9,830.78 - ₹28,463.29 per month
**Benefits**:
- Internet reimbursement
Schedule:
- Day shift
Supplemental pay types:
- Performance bonus
Ability to commute/relocate:
- Pune, Maharashtra: Reliably commute or willing to relocate with an employer-provided relocation package (required)
**Experience**:
- total work (preferred)
Application Deadline: 25/02/2023
-
Pharmacovigilance Associate
1 month ago
Pune, India Refined Reports Data Full timeA pharmacovigilance associate ensures compliance with applicable regulations or standard operating procedures; specialises in drug safety management, clinical trials and medical supervision. - Responsible for conducting, monitoring or reporting regular pharmacovigilance developments and supervising the processes related to ensuring drug effectiveness and...
-
Pharmacovigilance
4 weeks ago
Pune, India Refined Reports Data Full timeA pharmacovigilance associate ensures compliance with applicable regulations or standard operating procedures; specialises in drug safety management, clinical trials and medical supervision. - Responsible for conducting, monitoring or reporting regular pharmacovigilance developments and supervising the processes related to ensuring drug effectiveness and...
-
Pharmacovigilance Associate
4 days ago
Pune, India Statistical Pharma Full time**Primary Responsibilities**: 1. General Responsibilities and Regulatory Compliance: - Execute pharmacovigilance activities as nationally required (e.g. adverse event management, expedited and periodic reporting, risk management and creation and maintenance of the Pharmacovigilance System Master File). - Monitor national pharmacovigilance legislation. -...
-
Pharmacovigilance Associate
4 days ago
Pune, India Statistical Pharma Full time**Primary Responsibilities**: 1. General Responsibilities and Regulatory Compliance: - Execute pharmacovigilance activities as nationally required (e.g. adverse event management, expedited and periodic reporting, risk management and creation and maintenance of the Pharmacovigilance System Master File). - Monitor national pharmacovigilance legislation. -...
-
Pharmacovigilance Associate Fresher
1 month ago
Pune, India Excent Research Pvt. Ltd Full timeExcent Research is currently seeking to expand its Research and Development team for its Pharma Division. As part of this effort, we are actively recruiting for the positions of Pharmacovigilance Associates and Clinical Researchers. Eligibility: BSc, MSc, B Pharmacy, M Pharmacy, PharmD, Any UG / PG in Life Sciences **Job Types**: Full-time,...
-
Pharmacovigilance Associate
1 month ago
Pune, India Refined Reports Data Full timePharmacovigilance associates have a wide range of responsibilities, which can include: - Preparing reports of adverse drug reactions that may involve complex medical terminology, medical chart reviews, and statistical analyses - Responsible for monitoring potential side effects of drugs being marketed in the United States by reviewing case studies and...
-
Pharmacovigilance Associate
1 month ago
Pune, India Statistical Pharma Full timeProcessing adverse events reports from post marketing sources into Teva's global safety database: - The different sources / types of reports includes: Reports from the scientific literature, Teva partners (other pharmaceutical companies), Health Authorities, Non-interventional studies and other programs - The processing includes Adverse Events coding (in...
-
Pharmacovigilance Associate
1 month ago
Baner, Pune, Maharashtra, India Statistical Pharma Full time**Job description** - Responsible for review of investigational new drug safety reports (INDSR) and submission to FDA (as applicable) - Responsible for negotiation and implementation of pharmacovigilance agreements (PVA) with business partners - Supports PV Clinical Specialists in tasks and projects as needed - Responsible for identifying and developing...
-
Pharmacovigilance Associate
1 month ago
Pune, India Refined Reports Data Full timeProvide medical and clinical guidance to managers before, throughout, and following clinical trials. - Maintain consistency of safety assessments. - Perform a variety of safety assessments. - Serve in cross-functional teams as a medical and scientific representative. - Ensure regulatory compliance and safety throughout trial. - Submit periodic reports to the...
-
Pharmacovigilance Associate
1 month ago
Wagholi, Pune, Maharashtra, India Statistical Pharma Full time**Job description** - Responsible for review of investigational new drug safety reports (INDSR) and submission to FDA (as applicable) - Responsible for negotiation and implementation of pharmacovigilance agreements (PVA) with business partners - Supports PV Clinical Specialists in tasks and projects as needed - Responsible for identifying and developing...
-
Drug Safety Associate
4 weeks ago
Kharadi, Pune, Maharashtra, India Vertex Solutions Pvt Ltd Full timeThe primary duty of a Drug Safety Associate involves the ongoing monitoring and evaluation of adverse effects and safety concerns associated with drugs and medical products following market approval. As a Drug Safety Associate, your responsibilities will include monitoring, assessing, and reporting adverse events related to pharmaceutical products. You will...
-
Drug Safety Associate
2 days ago
Pune, India Fusion Technology Solutions Full timeTo write an effective drug safety associate job description, begin by listing detailed duties, responsibilities and expectations. We have included drug safety associate job description templates that you can modify and use. Sample responsibilities for this position include: Identify out of scope activities in conjunction with the MSS Functional...
-
Pharmacovigilance Associate
1 month ago
Pune, India Refined Reports Data Full timePreparing reports of adverse drug reactions that may involve complex medical terminology, medical chart reviews, and statistical analyses - Responsible for monitoring potential side effects of drugs being marketed in the United States by reviewing case studies and medical literature - Assisting in processing insurance claims for drug products dispensed by...
-
Pharmacovigilance Associate
2 months ago
Pune, India Bitwise Solutions Full timePreparing reports of adverse drug reactions that may involve complex medical terminology, medical chart reviews, and statistical analyses - Responsible for monitoring potential side effects of drugs being marketed in the United States by reviewing case studies and medical literature - Assisting in processing insurance claims for drug products dispensed by...
-
Cdm and Pv Executive
4 weeks ago
Pune, India Deloite Software Pvt Ltd Full timePharmacovigilance is science and practises involved in the identification, evaluation, comprehension, and mitigation of side effects and other medical/vaccination-related issues are referred to as harmacovigilance. Before being approved for use, all medications and vaccines go through extensive clinical trials to test their safety and...
-
Drug Safety Associate
1 month ago
Pune, India Fusion Technology Solutions Full timeDrug safety experts have numerous responsibilities and this can vary from one company to another. The roles include activities like. - Processing and writing of adverse event program - Follow up on important case reports - Serving as a link between company and the patients or healthcare experts to provide valid information on product safety. - Conducting...
-
Executive Director, SERM Head
4 days ago
Pune, India 12371 GSK Vaccines S.r.l. Full timePosition summary The Executive Director, Safety Evaluation & Risk Management (SERM) Head is accountable to lead SERM (Safety Evaluation & Risk Management) medical and scientific staff and define and drive the strategy and vision of clinical safety and pharmacovigilance activities in alignment with Global Safety business strategies. Competencies ...
-
Pharmacovigilance Associate
1 month ago
Pune, India PrimeVigilance Full timeJob DescriptionResponsibilities include: Processing of Individual Case Safety Reports from all sources (post-marketing and clinical trials) in compliance with applicable regulations, PrimeVigilance procedures and in accordance with client specific requirements and timelines, focusing on triage, data entry, quality review and submissions workflow...
-
Pharmacovigilance Associate
4 weeks ago
pune, India PrimeVigilance Full timeJob DescriptionResponsibilities include: Processing of Individual Case Safety Reports from all sources (post-marketing and clinical trials) in compliance with applicable regulations, PrimeVigilance procedures and in accordance with client specific requirements and timelines, focusing on triage, data entry, quality review and submissions workflow steps. ...
-
Process Executive
2 days ago
Pune, Maharashtra, India Cognizant Full time**Team Lead - CDM/PV** **Qualification**: Graduate/Post Graduate/ Doctorate degree in life sciences/Pharmacy/Medical sciences/Registered Nurse ** Responsibility**: **Business/ Customer**: - Minimal Customer interaction under guidance. - Understands Domain Process/sub process, functions, terminologies (such as SOP, QC checklists). - For PV/Complaints...