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:

09-16-2026

Salary:

$75 - $80 Per Hour

Job ID:

40029

Project Manager, Drug Safety, MI, and Pharmacovigilance

Join a dynamic 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, vendor transitions, and multi-affiliate platform integrations, ensuring seamless operational readiness and compliance. If you are a proactive, hands-on project management expert with a proven track record in structured methodologies, this is your chance to make a significant impact on critical product launches and regulatory milestones.

Key Responsibilities:

  • Lead end-to-end project execution, utilizing Waterfall methodologies to manage schedules, dependencies, and risks.
  • Drive proactive stakeholder engagement across multiple business units to uncover untracked deliverables and requirements.
  • Develop and implement structured onboarding procedures and training pathways for future affiliate integration.
  • Oversee and coordinate system and data migrations, ensuring timely completion ahead of key deadlines.
  • Lay the groundwork in Q1 for upcoming product launches scheduled for April, ensuring smooth project transitions.

Required Skills:

  • Demonstrated success as a hands-on, execution-driven Senior Project Manager with a full ownership approach.
  • Extensive experience managing projects in complex, structured environments using Waterfall methodologies.
  • Exceptional communication skills with the ability to engage senior leadership and cross-functional teams.
  • Strong background in managing technical and business system integrations and establishing operational interoperability.

Nice to Have Skills:

  • Exposure to Life Sciences, Pharma, Biotech, or MedTech environments.
  • Familiarity with Pharmacovigilance (PV), Medical Information (MI), or safety database implementations.
  • Experience in legacy data transfers and system validation processes.

Preferred Education and Experience:

  • Bachelor’s degree in Life Sciences, Business, or related field; advanced degrees preferred.
  • Minimum of 5 years of project management experience within regulated environments, particularly in pharmacovigilance or medical information systems.

Other Requirements:

  • This position is remote, offering flexibility in working location.
  • Ability to manage multiple priorities with tight deadlines, including upcoming regulatory commitments.
  • Willingness to participate in project meetings across different time zones as needed.

Be a driving force behind critical system upgrades and launches, ensuring operational excellence in a fast-paced, high-growth environment.

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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