IQVIA looking for PV Scientist

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 : PV Scientist

Job description
Job Overview
Apply knowledge and expertise for Safety Aggregate Report and Analytics (SARA) Center deliverables including safety aggregate reports, literature surveillance, signal management activities and benefit risk management documents.

Essential Functions
• Serve as principal owner of the SARA deliverable and have responsibility for completion of the deliverable in compliance with all applicable service level agreements (SLA).
• Lead, author and finalize aggregate reports, including but not limited to PBRERs/PSUR, DSURs, PADERs, RMPs, ACOs, and line listings
• author responses to regulatory agency/ Pharmacovigilance Risk Assessment Committee (PRAC) inquiries, as required.
• Conduct/Lead ongoing literature safety surveillance for marketed and investigational products. Assist with the identification of ICSRs from literature, evaluation of events of special interests as well as aggregate data review.
• Act as Signal Management Lead on post-marketing and clinical trial projects. Set-up, implement, organize (including documentation) and lead safety management teams. Set-up and update products' signaling strategies. Author and/or QC review all types of signal management deliverables. Lead/ conduct ongoing signal detection activities as per agreed signaling strategies, perform signal validation and signal evaluation analyses for proactive and timely identification of signals and characterisation of risks . Responsible for full documentation and tracking of signals.
• In a PV support role, lead/author and/or QC review safety responses to regulatory agencies/PRAC and justification documents to support labelling documents.
• Interface with clients and other functional groups within Lifecycle Safety and other business units, such as Regulatory affairs 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.
• Participate in internal and external audits and inspections, as required.
• Contribute to achievement of departmental goals e.g. utilization realization and productivity metrics.
• Read, acknowledge and adhere to all necessary IQVIA standard operating procedures (SOPs) and customer SOPs as required. Ensure all required training is executed in a timely fashion and documented.
• Serve as the interface between the global project lead and the working team
• conduct regular lessons learned with the working teams to ensure all information from the customer is cascaded to the relevant team members.
• Provide mentorship and training to less experienced resources.
• Provide regular reports to overall project manager and department management on project metrics, SOW changes, client requests or concerns
• participate in project review meetings with management
• communicate and document project issues to project team members and department management in a timely manner. Ensure Good Documentation Practices (GDP).
• Support and/or contribute to technology / innovation activities.

Candidate Profile
• Bachelor's Degree Bachelor's Degree
• 2 - 3 years relevant work experience.
• Equivalent combination of education, training and experience.
• Excellent knowledge of Lifecycle Safety services and processes.
• willingness and aptitude to learn new skills across Lifecycle Safety service lines.
• In depth knowledge and understanding of applicable global, regional, local regulatory requirements.
• i.e. Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP) and International Conference of Harmonization (ICH) guidelines, SOPs.
• Proven ability to meet strict deadlines.
• manage competing priorities and ability to be flexible and receptive to changing demands.
• Excellent organizational skills and time management skills.
• Good working knowledge of Microsoft Office and web-based applications (e.g., Word, Excel, Powerpoint).
• Good knowledge of medical terminology.
• Proven ability to follow instructions/guidelines, work independently and on own initiative.
• Excellent attention to detail and accuracy maintaining consistently high quality standards.
• Excellent written/verbal communication and report writing skills.
• Sound judgment.
• independent thinking and decision making skills.
• Self-motivated and flexible.
• Ability to establish and maintain effective working relationships with coworkers, managers and clients.
• Effective mentoring and coaching skills.
• Good understanding of operational metrics, productivity and initiatives.
• Demonstrate effective project management and leadership skills.

Additional Information
Experience : 2 - 3 years
Qualification : Bachelor's Degree
Location : Bangalore
Industry Type : Pharma / Healthcare / Clinical research
Job ID : R1268004
End Date : 20th February, 2022