skillindiajobs
Hyderabad Jobs
Banglore Jobs
Chennai Jobs
Delhi Jobs
Ahmedabad Jobs
Mumbai Jobs
Pune Jobs
Vijayawada Jobs
Gurgaon Jobs
Noida Jobs
Oil & Gas Jobs
Banking Jobs
Construction Jobs
Top Management Jobs
IT - Software Jobs
Medical Healthcare Jobs
Purchase / Logistics Jobs
Sales
Ajax Jobs
Designing Jobs
ASP .NET Jobs
Java Jobs
MySQL Jobs
Sap hr Jobs
Software Testing Jobs
Html Jobs
IT Jobs
Logistics Jobs
Customer Service Jobs
Airport Jobs
Banking Jobs
Driver Jobs
Part Time Jobs
Civil Engineering Jobs
Accountant Jobs
Safety Officer Jobs
Nursing Jobs
Civil Engineering Jobs
Hospitality Jobs
Part Time Jobs
Security Jobs
Finance Jobs
Marketing Jobs
Shipping Jobs
Real Estate Jobs
Telecom Jobs

Pharmacovigilance Associate

10.00 to 20.00 Years   Coimbatore   29 Dec, 2022
Job LocationCoimbatore
EducationNot Mentioned
SalaryRs 4.5 - 10 Lakh/Yr
IndustryMedical / Healthcare
Functional AreaPharmacist / Medical RepresentativeMedical Transcription
EmploymentTypeFull-time

Job Description

    Pharmacovigilance is the process of collecting, researching, monitoring, evaluating and assessing information derived directly or indirectly from patients to identify adverse effects of marketed medications and ensure drug safety. The aim of pharmacovigilance is to identify new hazards associated with medications and provide effectively safer medicines to the public.Advanced safety features and progression in medical technology have evoked interest in science graduates to apply for jobs associated with drug related issues. The unique and specialised nature of the job of pharmacovigilance associate attracts many degree holders to pursue a career in this line. A degree in medicine, nursing or life science is essential to become a pharmacovigilance associate. Working experience in a medical setting of a hospital or pharmacy provides a competitive edge for acquiring position of pharmacovigilance associate.Role and responsibilities
    • A 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 avoiding adverse effects or side effects of marketed pharmaceutical products among the general population in research trials and hospitals.
    • Pharmacovigilance associate aim at reducing the risks associated with administering and prescribing drugs along with improving safety and treatment outcome in patient care.
    • The role includes activities of important case report follow-up; processing and writing adverse event programs; serving link between the company, healthcare experts and patients for delivery of valid information on product safety;
    • Conducting and supervising regular pharmacovigilance processes; attending several product safety meetings and adding functionality to product safety.
    • A pharmacovigilance associate monitors all products and conducts post-market evaluations to ensure drug safety. These experts are actively involved in assessing adverse event writings, updating reports on safety, conducting quality and conveying drug related case reports to appropriate authorities.
    • Pharmacovigilance Associate plays an important role in research, development and testing of new medications in the pharmaceutical industry.
    • Responsible for global pharmacovigilance activities to support data safety and case tracking; perform document archiving; assist in the administration of pharmacovigilance meetings; support quality of review documents and initiate business liaison.
    • Other essential duties include drafting pharmacovigilance agendas and meeting minutes; accurately archiving pharmacovigilance documents; reviewing safety case data and other pharmacovigilance documents for completeness and accuracy; monitoring periodic safety reports through quality review of safety data and project management; assisting with tracking, submitting and distributing of periodic reports; assisting liaisons with the partners and cross-functional team members to ensure compliance; supporting various ad-hoc deliverables or pharmacovigilance projects; and conducting regulatory inspections.

Keyskills :
clinical chemistryclinical researchdrug safetyclinical trialsmedical writingpharmacovigilancepharmaceutical quality control

Pharmacovigilance Associate Related Jobs

© 2020 Skillindia All Rights Reserved