Safety Aggreg Report Mng /Senior PV Scientist

IQVIA; Bellville (TX); On-site; USD 55,000 - 79,000; Full time

Job summary

IQVIA seeks an experienced Safety Aggregate Report and Analytics (SARA) Center lead to drive global aggregate reports, signal management and literature surveillance. You will guide lifecycle safety processes, mentor teams, and ensure compliance with SOPs and regulatory expectations.

The role demands strong pharmacovigilance expertise, excellent communication, cross-functional leadership, and ability to deliver high-quality deliverables across projects and audits.

Qualifications

• 5-10 years of pharmacovigilance experience including drug safety and aggregate reports.
• Excellent communication (written and verbal) skills.
• Fluency in English (spoken and written).

Responsibilities

• Serve as stand-alone global lead for aggregate reporting, signal management, or literature surveillance projects.
• Lead, author and finalize reports (PBRERs/PSURs, DSURs, PADERs, RMPs, REMS, etc.).
• Author responses to regulatory inquiries as required.
• Mentor and coach SARA staff; provide training on deliverables.
• Oversee signaling strategies and data mining methodologies across projects.
• Ensure project documentation, compliance, and KPI reporting for audits.

Skills

Pharmacovigilance

Safety reporting

PBRER/PSUR

Regulatory liaison

Communication

Team leadership

English fluency

Education

Life science degree

Job description

Belgrade, Serbia
Budapest, Hungary
Bloemfontein, South Africa
Zagreb, Croatia
Athens, Greece
Centurion, South Africa
Sofia, Bulgaria
Bellville, South Africa
Evosmos, Greece
New Cairo, Egypt
Bucuresti, Romania

Full time
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Job Overview

Act as a stand-alone global functional lead at a project level applying experience, knowledge and expertise for Safety Aggregate Report and Analytics (SARA) Center deliverables including but not limited to safety aggregate reports, literature surveillance, signal management activities and benefit risk management documents. Actively contribute to Lifecycle Safety global process initiatives and work in close collaboration with the safety customer delivery management team regarding project/client initiatives. Ensure team is following standard best-in-class practices established by the SARA infrastructure.

Essential Functions

• Serve as a stand-alone global lead for aggregate reporting, signal management, or literature surveillance projects.
• Lead, author and finalize aggregate reports, including but not limited to PBRERs/PSURs, DSURs, PADERs, RMPs, REMS, ACOs, line listings
• and author responses to regulatory agency / Pharmacovigilance Risk Assessment Committee (PRAC) inquiries, as required.
• Act as literature lead, back-up lead, reviewer/QCers to conduct ongoing literature safety surveillance for marketed and investigational products. Assist with the identification of IC ...
• Act as Signal Management Lead on large and/or complex post-marketing and clinical trial projects. Set-up, implement, organize (including documentation) and lead safety management teams. Serve as subject matter expert across projects for complex data mining methodologies and algorithms on internal and external safety data sources. Oversee/set-up and update products' signaling strategies. Oversee/author and/or QC review all types of signal management deliverables.
• Oversee/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 . Accountable for full documentation and tracking of signals. At project level, maintain compliance, prepare metrics and KPI, present at audits and inspections.
• In a PV support role, act as functional lead and oversee/author and/or QC review safety responses to regulatory agencies/PRAC and justification documents to support labelling documents.
• Provide training to SARA staff for qualification on SARA deliverables
• May perform quality check of all assigned SARA deliverables
• be responsible for the quality of the final SARA deliverable to client regulatory, IQVIA regulatory reporting (RR), and regulatory authorities.
• Provide consultative guidance to internal and external stakeholders in the for all SARA deliverables.
• Act as mentor to and coach to project team staff and direct line reports.
• 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), Business development (BD) and Proposals, and Information Technology (IT), as needed
• Participate in internal and external audits, as required. Lead audit preparation activities in advance to audit and ensure audit readiness of project
• Review project files and contact lists on a regular basis to ensure compliance with SOPs
• Lead functional team and contribute to achievement of departmental goals e.g. utilization realization and productivity metrics.
• Read and acknowledge all necessary IQVIA standard operating procedures (SOPs) and customer SOPs as required. Ensure all required training is executed in a timely fashion and documented. Ensure Good Documentation Practices (GDP).
• Serve as the interface between the global project lead and the working team
• conduct regular lessons learnt 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, statement of work (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.
• Contribute to resource needs and resource allocation based on workload to ensure appropriate compliance with report submissions.
• Build a positive, collaborative team environment with SARA team members, lead by example and provide training and mentoring for local project leads and less experienced team members.
• Contribute and assist in global/local working groups as applicable in implementation of new operational initiatives, identification and implementation of process efficiencies.
• Participate in the review of existing standard operating procedures (SOPs).
• Proactively identify issues and propose solutions.
• Provide consultative guidance to internal and external stakeholders for all SARA deliverables.
• Suggest, drive, and implement continuous process improvements across all SARA center services.
• Collaborate with line managers to resolve project performance related issues of staff.

Qualifications

• Life science graduate/post-graduate, pharmacy, nursing, or other healthcare related qualification or experience in pharmacovigilance
• 5-10 years of relevant experience in Pharmacovigilance including hands-on experience of drug safety, aggregate reports, signal detection/signal management preferred
• Excellent communication (written and verbal) skills
• Strong organizational and time management skills. Proven ability to meet strict deadlines
• Manage competing priorities and ability to be flexible and receptive to changing demands
• English - fluent (spoken, written)

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

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