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 most precise way for evaluation of the relevancy of Clinical Research. In this the tests are conducted under observation whether a new innovative product performs as expected or not. There is ‘n’ number of innovative therapies generated in laboratories but very few of them survive & reach to the point of human testing. It...

As a Pharmacovigilance Associate you are part of the Pharmacovigilance Department (sometimes called the Drug Safety Department). Your role is one of reporting adverse effects (AEs) and side effects, in accordance with the current Dutch and European legislation for pharmacovigilance. You may also train colleagues in departments such as marketing and sales,...

As a Pharmacovigilance Associate you are part of the Pharmacovigilance Department (sometimes called the Drug Safety Department). Your role is one of reporting adverse effects (AEs) and side effects, in accordance with the current Dutch and European legislation for pharmacovigilance. You may also train colleagues in departments such as marketing and sales,...

**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. -...

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. - Ensure appropriate interpretation...

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. - Ensure appropriate interpretation...

A career in pharmacovigilance provides good prospects with generation of new drugs evey day. Pharmacovigilance is the process of collecting, reseraching, monotoring, evaluating and assessing information delivered directly or indirectly from patients. **Job Types**: Full-time, Fresher **Salary**: ₹15,000.00 - ₹25,000.00 per month **Benefits**: - Cell...

**Writing generic RMPs (data collection, Log of changes preparation, validation of finalised RMP)**: - **Coordinating simple generic RMPs** - **Drafting of responses to requests from regulatory agencies concerning RMP, as needed**: - **Ensuring that all tasks are performed in line with relevant predefined procedures**: - **Cooperation with other other...

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 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 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...

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...

Processing Individual Case Safety Reports (ICSRs) from all sources in compliance with applicable regulations, and in accordance with client specific requirements and timelines - Performing ICSR follow up - SAE/SUSAR Management (unblinding, clinical trial reconciliation, protocol review, Safety Management Plan review) - Reconciliation (clinical, partners) -...

**Job description** - 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...

**Job description** **Roles and Responsibilities** - In this role, you are required to solve routine problems, largely through precedent and referral to general guidelines - Your primary interaction is within your team and your direct supervisor - You will be given detailed instructions on all tasks that need to be carried out, and the decisions that you...

Job Description Skills: Clinical Research, Clinical, Research, CR, Pharmacovigilance, Regulatory Affairs, Clinical Trials, As a Senior CRA, you will participate in the preparation and execution of Phase I-IV clinical BA/BE studies with a particular focus on monitoring and site management activities to ensure timelines and deliverables are met at assigned...

About EVERSANAEVERSANA is a global company that delivers next-generation commercialization services to the life sciences industry. Our team of over 7,000 employees is dedicated to creating and delivering innovative solutions to bring therapies to market.The PositionThis role supports the client Pharmacovigilance Department as both a team member and...