Pharmacovigilance Associate

We are seeking a highly motivated and detail-oriented recent graduate to join our Pharmacovigilance team as an Entry-Level Pharmacovigilance Associate. This is a fantastic opportunity to begin your career in the pharmaceutical industry and contribute to the safety monitoring of our products. You will gain hands-on experience in various aspects of...

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...

Pharmacovigilance Responsibilities-Monitoring and documenting adverse events and product complaints.Collaborating with cross-functional teams to ensure compliance with safety regulations.Preparing and submitting safety reports to health authorities.Contributing to the development of pharmacovigilance processes and procedures.Staying up-to-date with evolving...

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. -...

**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...

Basic understanding of pharmacovigilance processes and regulatory requirements. - Strong attention to detail and accuracy in data entry and report preparation. - Ability to work in a team and follow instructions from senior professionals. - Proficiency in MS Office (Word, Excel, PowerPoint). - Good written and verbal communication skills. - Eagerness to...

Provide 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...

Collect, review, and process adverse event reports from clinical trials and post-marketing sources. - Perform data entry of case details into safety databases accurately and within timelines. - Assist in coding adverse events, medical history, and medications using MedDRA and WHO-DD. - Support literature screening for identification of safety signals. -...