Project Manager, Drug Safety, MI, and Pharmacovigilance

Project Manager, Drug Safety, MI, and Pharmacovigilance

Contract Type:

Contract

Location:

San Francisco - CA

Industry:

Information Technology

Contact Name:

Contact Email:


Contact Phone:


Date Published:

09-19-2026

Salary:

$75 - $80 Per Hour

Job ID:

40028

Job Title: Project Manager, Drug Safety, MI, and Pharmacovigilance

Overview:
Join a dynamic, innovative life sciences organization as a Project Manager specializing in Drug Safety, Medical Information, and Pharmacovigilance. This pivotal role offers the opportunity to lead complex system implementations, facilitate vendor transitions, and drive multi-affiliate platform integrations. Perfect for a proactive, hands-on project management professional, you will work closely with senior leadership to ensure successful onboarding, milestone achievement, and regulatory compliance, supporting critical product launches and future growth initiatives.

Required Skills:

  • Proven success as a hands-on, execution-oriented Senior Project Manager capable of managing end-to-end project delivery.
  • Expertise in Waterfall project management methodologies within complex, structured environments.
  • Exceptional communication skills, with the ability to engage executive stakeholders and resolve issues proactively.
  • Strong background in managing cross-functional systems integration, ensuring operational interoperability.
  • Ability to independently track progress, identify risks, and manage project dependencies efficiently.

Nice to Have Skills:

  • Knowledge or experience within Life Sciences, Pharma, Biotech, or MedTech sectors.
  • Familiarity with Pharmacovigilance (PV), Medical Information (MI), or safety database platforms.
  • Experience with data migration, system validation, and regulatory compliance in drug safety environments.

Preferred Education and Experience:

  • Bachelor’s Degree in Life Sciences, Pharmacy, or related field; advanced degrees or relevant certifications are a plus.
  • Minimum 5+ years of project management experience, ideally in regulated healthcare or pharmaceutical settings.
  • Prior involvement with safety systems such as Argus, ArisG, or comparable PV platforms.

Other Requirements:

  • This position is remote, with the expectation to occasionally collaborate with global teams.
  • Excellent organizational skills and ability to meet tight deadlines, including critical regulatory milestones.
  • Willingness to adapt to evolving project needs and timelines, with a focus on quality and compliance.

This is an exceptional opportunity to impact the future of drug safety and pharmacovigilance processes within a forward-thinking organization.

DeWinter Group and Maris Consulting  is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. We post pay scales which are based on our client pay ranges. DeWinter, Maris, and our clients have the right to modify the requirements of the role which can impact the pay ranges posted.

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