IQVIA Career Opportunity: Join as PV Safety Aggregate Report Specialist-I – Elevate Your Impact in Healthcare

Welcome to a career opportunity that merges expertise with impact! IQVIA is thrilled to extend an invitation for talented professionals to join our team as PV Safety Aggregate Report Specialist-I. As a pivotal player in the field, IQVIA is at the forefront of driving innovation and excellence in pharmacovigilance.

If you are a dedicated individual with a passion for ensuring drug safety and a keen eye for detail, this role as PV Safety Aggregate Report Specialist-I is tailor-made for you. Join us in shaping the future of healthcare by contributing to the safety assessment and reporting processes.

Position: PV Safety Aggregate Report Specialist-I

Job Overview
Serve as principal owner of the SARA deliverable and have a responsibility to complete the deliverable in compliance with all applicable service level agreements.

Essential Functions
1. Act as primary author & or reviewer/QCer of SARA deliverables involving aggregate reports, signal management or literature review projects.
2. Lead, author and finalize small to medium aggregate reports, including but not limited to PBRERs/PSURs, DSURs, PADERs, ACOs, device reports, and line listings
3. Author. Responses to regulatory agency/ Pharmacovigilance Risk Assessment Committee (PRAC) inquiries, as required.
4. Act as literature lead, backup lead, and reviewer/QCers to contribute to conducting ongoing literature safety surveillance for marketed and investigational products with the identification of ICSRs from literature, evaluation of events of special interests, and aggregate data review. Author and/or contribute to literature deliverables for aggregate reports &/or signal management activities meeting strict regulatory timelines.
5. Act as Signal Management Specialist on post-marketing and clinical trial projects. Author all types of signal management deliverables. Conduct ongoing signal detection activities per agreed signalling strategies, perform signal validation and evaluation analyses for proactive and timely identification of signals and characterization of risks. Participate as a core member and present in safety management teams. Responsible for full documentation and tracking of movements.
6. In a PV support role, author safety responses to regulatory agencies/PRAC and justification documents to support labelling documents.
7. Interface with clients and other functional groups within Lifecycle Safety and other business units, such as Regulatory Reporting (RR), Real World Late Phase (RWLP), Medical Writing, Clinical Research, Quality, Knowledge Quality Management (KQM), Pharmacovigilance Support (PVS), Project Leads (PL), Medical Safety Advisors (MSA), Qualified Persons for Pharmacovigilance (QPPV) / Pharmacovigilance Contact at National Level (PCNL), Library Information Services (LIS), Safety Operations (SO), and Information Technology (IT), as needed.
8. Participate in internal and external audits and inspections, as required.
9. Contribute to achieving departmental goals, e.g. utilization realization and productivity metrics.
10. Read, acknowledge and adhere to all necessary IQVIA standard operating procedures (SOPs) and customer SOPs as required. Ensure all the essential training is executed promptly to maintain compliance and documentation.
11. Serve as the interface between the global project lead and the working team.
12. Conduct regular lessons learned with the operational teams to ensure all information from the customer is cascaded to the relevant team members.
13. Provide mentorship and training to less experienced resources.
14. Provide regular reports to the overall project manager and department management on project metrics, statement of work (SOW) changes, and client requests or concerns.
15. Participate in Project review meetings with management.
16. Communicate and document project issues to project team members and department management promptly.
17. Support and/or contribute to technology/innovation activities.

Qualifications
1. Bachelor’s Degree Bachelor’s Degree Req
2. 4+ years of relevant experience in drug safety, aggregate reporting, signal management, or literature surveillance. Pref
3. Equivalent combination of education, training and experience. Req
4. Good understanding of Standard Operating Procedures (SOPs) and work instructions applicable to the role. Intermediate
5. Good working knowledge of Microsoft Office and web-based applications (e.g., Word, Excel, Powerpoint). Intermediate
6. Good knowledge of medical terminology. Intermediate
7. Strong organizational skills and time management skills. Intermediate
8. Strong verbal/written communication skills. Intermediate
9. Self-motivated and flexible. Intermediate
10. Excellent attention to detail and accuracy. Intermediate
11. Ability to follow instructions/guidelines, utilize initiative and work independently. Intermediate
12. Proven ability to multi-task and manage competing priorities and deadlines. Intermediate
13. Willingness and aptitude for learning new skills across all Lifecycle Safety service lines. Intermediate

How to Apply
Interested may reach us at pavan.cm@iqvia.com

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