Pharmacovigilance Intern - Hyderabad

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPha ...

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. · ...

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 motivated and detail-oriented individual to join our team as a Pharmacovigilance Intern. This internship provides an excellent opportunity to gain hands-on experience in the field of pharmacovigilance, contributing to the advancement of healthcare solu ...

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 skilled and experienced Associate Pharmacovigilance Specialist to join our team in the Pharmaceutical and Life Sciences industry. The ideal candidate will have a strong background in pharmacovigilance and excellent analytical skills. · Roles and Respon ...

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

We are looking for a highly skilled and experienced professional to fill the role of Executive Regulatory Affairs & Pharmacovigilance. The ideal candidate will have a strong background in regulatory affairs and pharmacovigilance, with excellent communication and analytical skills ...

The ICSRs Project Lead will manage post-marketed pharmacovigilance projects, ensuring compliance with client contracts and applicable Standard Operating Procedures (SOPs) and Work Instructions (WIs). · Key Responsibilities: · Perform as the ICSRs Project Lead for assigned pharmac ...

Career Category · Safety · Job Description · 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. ...

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 ...

Career Category · Safety · Job Description · 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 intell ...

Key Accountabilities · General · Maintain knowledge of safety profiles, labeling, and global regulations · Implementation of project-specific procedures and workflows · Support compliance with regulatory reporting timelines · Assist with audit and inspection preparation · Review ...

This position is responsible for the maintenance and oversight of the PV System, ensuring adherence to local, regional, and global processes. · ...

Project Leadership: Serve as the ICSRs Project Lead for post-marketing pharmacovigilance projects, adhering to client contracts and applicable Standard Operating Procedures (SOPs) and Work Instructions (WIs). · Adverse Event Management: Oversee the receipt and processing of all ...

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPha ...

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

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 ...

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