Pharmacovigilance Intern - Hyderabad

We are offering an exciting internship opportunity in the Pharmacovigilance department for individuals with experience in the Argus safety database. This role will provide hands-on experience in drug safety processes, case management, and regulatory reporting. · Manage assigned m ...

We are seeking a Pharmacovigilance Intern to join our team at ProPharma Group. As an intern, you will assist in managing mailboxes, performing duplicate searches and data entry into safety databases. · ...

We are offering an exciting internship opportunity in the Pharmacovigilance department for individuals with experience in the Argus safety database. · ...

This is a full-time on-site role for a Graduate Pharmacovigilance Associate located in Noida. The role involves monitoring collecting and evaluating data on the safety of pharmaceuticals. · Strong knowledge of pharmacovigilance principles adverse event reporting and safety data e ...

We are looking for a highly skilled and experienced Pharmacovigilance Analyst to join our team at a reputed Pharma Company. · ...

We are looking for a highly experienced Pharmacovigilance Director / VP to lead our team in ensuring the safe and effective development of pharmaceutical products. · ...

The Pharmacovigilance Operations Senior Manager provides strategic leadership and operational oversight of the global safety system and associated data mart to ensure accurate compliant timely safety data analytics and reporting. · This role is accountable for driving system perf ...

The Pharmacovigilance Operations Senior Manager provides strategic leadership and operational oversight of the global safety system and associated data mart to ensure accurate, compliant, and timely safety data analytics and reporting. · Deep expertise in pharmacovigilance safety ...

The Pharmacovigilance Operations Manager supports the global safety system and associated data mart to ensure accurate, compliant, and timely safety data analytics and reporting. This role plays a critical role in inspection readiness, regulatory compliance, · Maste's degree OR B ...

The Pharmacovigilance Operations Manager supports the global safety system and associated data mart to ensure accurate, compliant, and timely safety data analytics and reporting, · while advancing the use of automation, artificial intelligence (AI), and innovative technologies wh ...

The Pharmacovigilance Operations Manager supports the global safety system and associated data mart to ensure accurate, compliant, and timely safety data analytics and reporting while advancing the use of automation artificial intelligence AI and innovative technologies where app ...

I'm looking for a Regulatory Affairs Specialist to oversee the preparation and submission of regulatory dossiers ensuring compliance and timely approvals. · ...

The Drug Safety Associate approves and schedules reports in the Argus database for submission to respective Health Authorities as applicable. · ...

Quality Review and Submissions drug safety associate ICSR job for company involves approving scheduling reports in Argus database submission to Health Authorities as applicable submitting cases to Health Authorities Business Partners Affiliates required ensuring adherence interna ...

This individual will support interactions with business partners (license partners) and vendors for all case intake and processing activities. ...

Support interactions with business partners and vendors for all case intake and processing activities. · Ensure vendor compliance with approved processes and training requirements. · Act as US/EU local safety office and FDA/EMA point of contact for safety reporting. ...

The PC Triage and Intake Associate is responsible for global triage of Product Complaints and ensure proper Adverse Events and/or Other Safety Findings were captured. Ensure to capture the patient outcome because of the reported event. · ...

Drug Safety Physician provides medical review and analysis during case handling and reporting cycle for Individual Case Safety Reports and ADR reports. · ...

Enter information into PVG quality and tracking systems for receipt and tracking ICSR as required. Assists in the processing of ICSRs according to Standard Operating Procedures (SOPs) and project/program-specific safety plans as required. · B.Pharm/M.Pharm onlyOffice Location: Hy ...

Provide medical review analysis and guidance during the case handling and reporting cycle of Individual Case Safety Reports and ADR reports for investigational and marketed products. · MBBS , MD in Pharmacology · ...