Drug Safety Associate

The Drug Safety Associate will process drug safety data, perform case processing, and contribute to safety signal detection and risk management activities.Roles & Responsibilities:Collect, review, and process Individual Case Safety Reports (ICSRs) from spontaneous reports, literature, and clinical trials.Enter safety data into pharmacovigilance databases...

Assist in development of project specific safety procedures, workflows and templates Assist in project specific safety database setup, development of data entry guidelines, and user acceptance testing Triage incoming reports for completeness, legibility and validity Electronic documentation and quality control of drug safety information Data entry of...

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.Each of us, no matter what we do at...

Job Title: Junior API R&D Chemist Company:Morepen Proprietary Drug Research Pvt. Ltd. (MPDRPL) Location:Gagillapur, Hyderabad. Apply at: About UsMorepen Proprietary Drug Research Pvt Ltd (MPDRPL)is a leading pharmaceutical research and development organization committed to innovation and the advancement of healthcare. We are dedicated to discovering and...

2600+ Aggregate Reports annually! Dynamic teams at Novartis are committed to scientifically evaluate benefit-risk profile of the marketed products and collaborate with Health Authorities towards the ultimate goal of Patient Safety. Your skills & experience will help us on our journey of re-imagining patient safety. - Your responsibilities include, but are...

**Responsibilities**: 3. Complete case entry including case narrative writing, coding from the MedDRA dictionary and WHO drug dictionary as per applicable SOPs and Client requirements. Perform Call handler/QC Reviewer activity as needed. Send the reviewed and signed TCFs/ CDRs to the Client’s point of contact (POC). 4. Responsible for adding/ updating new...

Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $2B in revenue in our last fiscal year with extensive growth potential ahead.At the heart of Veeva are our values: Do the Right Thing, Customer...

Job Description SummaryJoin Novartis as an Associate, Managed Access Programs (MAP) & Post-Study Drug Supply (PSDS) Operations and play a key role in supporting patient access to innovative therapies. You will contribute to the planning and execution of these programs, collaborating with global teams to ensure medicines reach those who need them -...

**Working with Us** Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...

Job Description Summary Join Novartis as a Senior Associate, Managed Access Programs (MAP) & Post-Study Drug Supply (PSDS) Operations and play a vital role in supporting patient access to innovative therapies. You will independently contribute to the planning and execution of these programs, collaborating with global teams to ensure medicines reach those who...