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hiring Pharmacovigilance Scientists for the ICSR & Aggregate Reporting process
about the company; Pro Pharma is a pharmaceutical company that specializes in providing innovative solutions to help healthcare organizations and insurance companies optimize their prescription drug benefit programs. The company was founded in 2001 and is headquartered in Chatsworth, California.
One of Pro Pharma’s primary goals is to help clients reduce their pharmacy benefit costs while still providing quality care to patients. They achieve this through a combination of advanced analytics, data mining, and clinical expertise. Pro Pharma’s team of experts analyzes claims data to identify trends and potential issues and then works with clients to develop customized strategies to address these issues.
Dear Applicant,
pro pharma is pleased to invite you for a walk-in interview at [ProPharma (ISaftey) on March 3 2023 at 10:30 AM IST.
hiring Pharmacovigilance Scientists for the ICSR & Aggregate Reporting process
Pharmacovigilance Scientists play a crucial role in the drug safety and risk management process by monitoring and evaluating the safety and effectiveness of medications throughout their lifecycle. One of the primary responsibilities of Pharmacovigilance Scientists is to oversee the collection, processing, and reporting of Individual Case Safety Reports (ICSRs) and Aggregate Reports.
ICSRs are reports of adverse events or other safety-related information associated with the use of a particular medication. Pharmacovigilance Scientists are responsible for reviewing and analyzing these reports to determine if any safety concerns exist and if any actions need to be taken to mitigate the risk.
Aggregate reports are summaries of safety data compiled from multiple sources, including clinical trials, post-marketing surveillance, and spontaneous reports. Pharmacovigilance Scientists are responsible for ensuring that these reports are accurate, complete, and up-to-date.
When hiring Pharmacovigilance Scientists for the ICSR and Aggregate Reporting process, it is important to look for candidates with a strong background in pharmacovigilance and drug safety, as well as experience in the collection, processing, and reporting of safety data. Candidates should also have a thorough understanding of regulatory requirements for safety reporting, including FDA and EMA guidelines.
Date & time; March 3 2023 at 10:30 AM IST.
VENUE; The interview will be held at our office located on the 07th floor, III blocks, MY HOME HUB, Hitech city, beside Hitech Metro station.
We believe that you possess the skills and qualifications that we are looking for in a candidate, and we are excited to meet you in person. During the interview, we will discuss your experience and qualifications, as well as the requirements of the position.
If you have any questions, please do not hesitate to contact us at [email protected]
We look forward to meeting you.
Best regards,
Ramya Sree
Talent Acquisition Manager
ProPharma.
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