Pharmacovigilance Systems Lead

Insight Global
Wilmington, DE, United States
24 days ago
Apply on dejobs.org
Prepare application

Role details

Contract type
Permanent contract
Employment type
Full-time (> 32 hours)
Experience level
Expert
Experience required
8 years minimum
Working hours
Regular working hours
Job source

Tech stack

Software Code Optimization Oracle (Applications) Smartsheet Sap Finance Veeva

Job description

We are seeking a senior Pharmacovigilance Systems Lead to support a global biotechnology organization during a critical Oracle Argus to Veeva Safety transformation. This individual will serve as a key SME for drug safety technology initiatives while partnering with business and IT leaders to drive implementation activities, stakeholder alignment, and project financial oversight. This role requires 3 days onsite in Wilmington, DE.

Responsibilities

  • Serve as a subject matter expert for pharmacovigilance and drug safety systems.
  • Support and help lead the migration from Oracle Argus to Veeva Safety.
  • Partner with Drug Safety, Regulatory, IT, and business stakeholders to ensure successful project delivery.
  • Manage project financials, including budgets, invoices, purchase orders, vendor coordination, and spend tracking.
  • Identify risks, drive issue resolution, and support ongoing system optimization efforts.
  • Provide leadership and guidance across pharmacovigilance technology initiatives.

We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global’s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.

Requirements

  • 8+ years of experience supporting Pharmacovigilance or Drug Safety systems in a pharmaceutical, biotechnology, or life sciences environment.
  • Experience with Veeva Safety, Oracle Argus, ArisGlobal, or similar pharmacovigilance platforms.
  • Experience supporting system implementations, upgrades, or migrations.
  • Strong understanding of drug safety business processes and regulated environments.
  • Excellent stakeholder management and communication skills. - Direct experience with Veeva Safety implementations or migration projects.
  • Experience managing project budgets and vendor-related activities.
  • Exposure to SAP Finance, Smartsheet, or similar tools.

Apply for this position

This job is hosted externally. Click below to view the full posting and apply.

Apply on dejobs.org
Prepare application

Good distractions

Talks and stories from around this role — technically off-topic, practically not.

1:06 min

Developer experience and project variety at scale

Alexandra Petri · World Congress 2023

1:56 min

Delivering pharmaceutical compliance via the Swap monolith

Matthias Kauzmann Matthias Kauzmann · Europe 2026 Virtual

1:44 min

Background and career journey in regulated software systems

Martin Hynie · Coffee With Developers

Videos

See all

Related articles

See all