Overview
Associate Scientific Director in medical communications, guiding medical writers, overseeing quality control and partnering with clients and key opinion leaders on evidence-based scientific content for pharmaceutical and biotech clients.
What you'll do
- Ensure all deliverables are evidence-based, strategically aligned and executed to the highest quality.
- Partner with a Scientific Director and Strategic Account Directors to translate client objectives into scientific content and programs.
- Guide medical writers and oversee the quality-control process.
- Contribute to strategic planning across projects.
- Engage directly with clients, authors and key opinion leaders to shape scientific narratives across therapeutic areas.
- Contribute to content development, regulatory review and advisory board planning.
- Identify opportunities for innovation and business growth.
What you'll need
- Advanced life sciences degree (MD, PhD or PharmD).
- 2–3+ years of experience within a medical communications agency.
- Demonstrated expertise in medical/scientific writing and content development.
- Exceptional written and verbal communication skills.
- Proven ability to manage multiple projects and timelines in a fast-paced environment.
- Experience collaborating with clients, key opinion leaders and cross-functional teams.
Nice to have
- Prior experience mentoring or managing medical writers.
- Exposure to regulatory review processes and advisory board development.
- Familiarity with competitive intelligence and therapeutic landscape analysis.
- Experience supporting new business development or client growth initiatives.
Details
- Location: Remote, United States.
- Eligible for a discretionary annual bonus, health insurance, retirement savings, life and disability insurance, parental leave and paid time off.
- Must be legally authorized to work in the country of employment without employer sponsorship.
Read the full description and apply on the company’s own careers page.