Pharmacovigilance Associate

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...

Pharmacovigilance is the process of collecting, monitoring, researching, assessing and evaluating information from healthcare providers and patients on the adverse effects of medications to ensure that drugs on the market are safe for patients and to identify new hazards associated with the medication. **Job Types**: Full-time, Regular /...

Pharmacovigilance is the process of collecting,monitoring resarching, assessing and evaluating information from healthcare providers and patients on the adverse effects of medications to ensure that drugs on the market are safe for patients and to identify new hazards associated with the medication. **Job Types**: Full-time, Regular / Permanent **Salary**:...

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...

A Drug Safety Associate is responsible for assessing the safety of pharmaceuticals drugs once they're on the market. Using standardised guidelines, they determine whether the medication causes any adverse reactions in patients and report their findings back to the pharmacovigilance department. **Job Types**: Full-time, Regular / Permanent,...

A Drug Safety Associate is responsible for assessing the safety of pharmaceuticals drugs once they're on the market. Using standardised guidelines, they determine whether the medication causes any adverse reactions in patients and report their findings back to the pharmacovigilance department. **Job Types**: Full-time, Regular / Permanent,...

A Drug Safety Associate is responsible for assessing the safety of pharmaceuticals drugs once they're on the market. Using standardised guidelines, they determine whether the medication causes any adverse reactions in patients and report their findings back to the pharmacovigilance department. **Job Types**: Permanent, Full-time, Fresher **Salary**:...

A career in pharmacovigilance provides good prospects with generation of new drugs every day. Pharmacovigilance is the process of collecting, researching, monitoring, evaluating and assessing information derived directly or indirectly from patients. **Job Types**: Full-time, Regular / Permanent, Fresher **Salary**: ₹15,000.00 - ₹25,000.00 per...

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 -...

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 medical literature - Assisting in processing insurance claims for drug products dispensed by...

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...

Manage the receipt and processing of all adverse event reports reported either spontaneously from any source or from a clinical trial. This includes, but is not limited to: - entry of safety data onto adverse event database(s) and tracking systems - review of adverse events for completeness, accuracy and appropriateness for expedited reporting - write...

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...