Opportunity for M.Pharm, M.Sc as Analyst at IQVIA

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IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.

Post : Analyst

Job Description
• Analysis, case intake and processing of  adverse events from diverse therapy areas in to clients’ safety systems, ensuring 100% accuracy by conforming to the SOPs
• Lay strong emphasis on quality, ensuring zero errors during all steps of ICSR processing
• Proficient in end to end case processing . Activities include : Data verification , Data entry , coding of adverse events and drugs , causality assessments , case narratives and quality assessments
• Exposure and proficient in working in ARISg and IRT / Argus/ any other safety databases
• Lay strong emphasis on quality, ensuring zero errors during execution and/or review of comments while analyzing adverse events
• Coordinate effectively with team members and stakeholders
• Ability to train other team members on case processing concepts / practices
• Willing to work on public holidays/weekends on rotation basis (if required)

Candidate Profile :
• Bachelor of Medicine, Bachelor of Surgery (MBBS) / Bachelor of Dental Surgery (BDS) / BSc in Nursing / B.Pharm / M. Pharm or any other relevant degree from a reputed university with 1-3 years of work experience in clinical research organizations/regulatory affairs in the pharma industry
• Case processing experience is a must
• Familiarity with workflows in PV safety databases/tools
• Logical reasoning and sound clinical background
• Basic knowledge and understanding of the pharmaceutical regulations (FDA/EMA) and standards (ICH)
• Excellent reading comprehension skills and attention to detail to ensure pristine quality
• Good verbal/written communication and ability to understand/interpret clinical data
• Computer proficiency (MS Office)
• Hunger to learn and adapt to new processes and global environments

Additional Information
Experience : 1-3 years
Qualification : M.Pharm, B.Pharm, B.Sc, BDS, MBBS
Location : Bengaluru, Karnataka
Industry Type : Pharma/ Healthcare/ Clinical research
Job Code : R1126530
End Date : 30th July, 2020

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