Pharmacovigilance Associate

**Job description** WHO defines Pharmacovigilance (PV) as the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other drug-related problem. Pharmacovigilance is also known as drug safety and it focuses on ADR (Adverse drug reaction).The main aim of Pharmacovigilance is to monitor approved...

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 training documents (i.e.,...

A Pharmacovigilance Associate plays a crucial role in ensuring adherence to relevant regulations and standard operating procedures. They oversee processes to ensure the effectiveness of drugs while minimizing adverse effects in both research trials and hospital settings. **Responsibilities**: - recording and reporting adverse reactions received from...

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 In summary, typical roles and responsibilities include...

We're seeking dedicated individuals to join our Drug Safety team as Entry-Level Drug Safety Associates. This role offers an exciting opportunity for recent graduates to kickstart their careers in pharmacovigilance and drug safety. **Responsibilities**: - Assist in collecting, processing, and evaluating adverse event reports and safety data. - Ensure...

Company Description We are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider initially established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory...

Full Time Mumbai Posted 10 hours ago To plan and Manage Medical Writing for Regulatory and Pharmacovigilance Verticals in compliance to applicable regulatory and Regulatory Guidelines Duties and responsibilities To plan and Manage Medical Writing for Regulatory and Pharmacovigilance Verticals in compliance to applicable regulatory and Regulatory...

**Site Name**: India - Maharashtra - Worli Mumbai **Posted Date**: May 13 2024 Medical Scientific Liaison - Adult Vaccines (Mumbai) - Develop and sustain credible networking with appropriate Health Care Practitioners (HCPs) - Plan, facilitate and conduct CMEs, symposia, trainings, workshops, scientific meetings, speaker tours, and other product specific...

Pune, India - DOP - 3054658 **Job Description**: **Role - Writer Role** **Location - Pune** **Education Qualification-** **Mpharm., Bpharm., pharmD **Experience-** **6 months-1 Yrs. **Notice Period-** **Immediate -30 Days Roles & Responsibilities: ** Role & Responsibility** - 1. Reviewing the published reports/biomedical literature to ascertain if they...

Medical Scientific Liaison – Adult Vaccines (Mumbai) Develop and sustain credible networking with appropriate Health Care Practitioners (HCPs) Plan, facilitate and conduct CMEs, symposia, trainings, workshops, scientific meetings, speaker tours, and other product specific campaigns and deliver scientific presentations with consistent messages for key...

Medical Scientific Liaison – Adult Vaccines (Mumbai) Develop and sustain credible networking with appropriate Health Care Practitioners (HCPs) Plan, facilitate and conduct CMEs, symposia, trainings, workshops, scientific meetings, speaker tours, and other product specific campaigns and deliver scientific presentations with consistent messages for key...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

**Working with Us** Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...

**Roles and Responsibilities in detail** **Area Business Planning**: - Plan for monthly and quarterly business. - Plan for Trade activation business and over all sales - Plan demand generation and fulfillment - Monitor actual Sales and mid course corrections and inputs to reduce variance against expectations - Prescription audit for Abbott brands and other...

105,000 people reimagining medicine for more than 766 million people globally. To provide country clinical strategic guidance and feasibility assessment for GDD trials. Your responsibilities include, but are not limited to - To provide clinical strategic and tactical leadership in the country to support GDD trials, clinical development plans which change the...