Director, US Medical Information & Medical Review

Your contribution:
- Medical Review Leadership: Lead medical review processes for promotional and non-promotional materials and scientific communications; set priorities aligned with regulatory requirements, ethical standards, and scientific excellence.
- Process Development and Optimization: Design, implement, and refine medical review frameworks and SOPs; modernize legacy systems into scalable processes.
- Workstream Management: Build and manage agile cross-functional workstreams; drive efficiency and accountability.
- Team Leadership: Mentor and lead a matrixed team of medical reviewers, information specialists, and project managers.
- Cross-Functional Collaboration: Partner with Regulatory, Legal, Compliance, Commercial, and Scientific Affairs.
- Medical Information Oversight: Deliver scientifically accurate medical information; lead inquiry response, content creation, and knowledge management.
- Quality Assurance & Compliance: Ensure audit readiness and risk mitigation.
- Change Management: Drive continuous improvement in medical review and information practices.
- Metrics & Reporting: Define and monitor KPIs; provide insights to executive leadership.

A good match:
- 8+ years pharmaceutical/biotech experience; 5+ years in medical affairs.
- PharmD/PhD/MD or equivalent strongly preferred.
- Experience developing medical review processes and multidisciplinary workstreams.
- Knowledge of regulatory/compliance requirements (e.g., EFPIA, FSA, PhRMA).
- Proven leadership in matrixed teams.
- Exceptional communication, negotiation, and stakeholder management.

Preferred qualifications:
- Experience with digital content review systems and project management tools.

Your benefits and remuneration:
- Expected pay range: $168,100/year to $268,700/year + benefits, annual bonus & equity (variable).

Apply now:
- Apply for the New Jersey, US location using the online form.