Pharmacovigilance Associate Life Science Fresher

Excent Research is currently seeking to expand its Research and Development team for its Pharma Division. As part of this effort, we are actively recruiting for the positions of Pharmacovigilance Associates and Clinical Researchers. Eligibility: BSc, MSc, B Pharmacy, M Pharmacy, PharmD, Any UG / PG in Life Sciences **Job Types**: Full-time,...

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,...

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...

Clin Infotech is offering the internship opportunity for BDS MDS Dental GraduatesShould have Knowledge in Pharmacovigilance Should Have knowledge on Argus & MEDDRAApplicants Should Complete Certification in Pharmacovigilance Required Candidate profileB.Pharm / M.Pharm/Pharm D/Life sciences degree With Hands On Experience On Argus Safety Database and Med DRA...

TCS is hiring PharmacovigilanceJob Location: PuneExperience Range : 2 - 6 YearsEducational Qualification(s) Required: Any Life Science graduateRequired Skillsets:Ability to understand and analyses the complex data and performs the activities including accessing the case in Argus, code and enter data.Be fully competent to perform all steps within the...

**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. -...

Job description - Provide high quality, balanced and timely information to requests for medical information from both internal and external customers. - Maintain a database of Medical Information requests and responses. - Develop and maintain current knowledge of products and disease states. - Maintain references and other Medical Information resources. -...

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. -...

**Key Responsibilities** - Conduct training sessions on Individual Case Safety Reports (ICSR) and pharmacovigilance processes. - Develop and deliver presentations to enhance team knowledge. - Ensure compliance with Good Pharmacovigilance Practices (GVP) and regulatory requirements. - Mentor new joiners and assess trainee performance. - Provide expertise on...

Company Description We are PrimeVigilance (part of Ergomed Group), 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...