As a Medical & Scientific Affairs Advisor, you will serve as a scientific and imaging expert, partnering across functions to support high-quality independent image review, regulatory readiness, and innovation in clinical research, helping bring life-changing therapies to patients faster.
What We Offer- Competitive compensation
- Comprehensive health, dental, and vision coverage
- Retirement savings plan with company contribution
- Paid time off and company holidays
- Flexible work arrangements (role dependent)
What You'll Be Doing- Serve as an imaging advisor supporting company operations and initiatives across assigned therapeutic areas.
- Provide scientific input on clinical trial design, image review methodology, and image data quality control.
- Manage and enhance processes for independent image review, ensuring consistency, quality, and regulatory readiness.
- Monitor, review, and communicate industry trends related to independent review to maintain service leadership.
- Implement training standards for new radiologists, study-specific needs, and emerging imaging criteria.
- Contribute to scientific publications, abstracts, editorials, and thought leadership initiatives.
- Identify and implement innovations to improve central read efficiency and interpretation techniques.
- Create, review, and maintain imaging documentation, including charters, imaging manuals, and study-specific rules.
- Develop operational strategies for new imaging criteria and modalities, including nuclear medicine (e.g., PET/CT).
- Support radiopharmaceutical trials, specialized client requests, CMO review processes, sponsor audits, and regulatory inspections.
- Partner with application development and business development teams to translate scientific requirements into operational and client-facing solutions.
- Lead, mentor, and develop team members through training, coaching, and performance guidance.
What We Look For- Bachelor's degree required; advanced degree preferred, or equivalent practical experience.
- 5+ years of experience in clinical trials and/or the pharmaceutical environment.
- Demonstrated expertise in multi-modality imaging projects; medical imaging software experience preferred.
- Strong understanding of imaging criteria, clinical trial operations, and regulatory expectations.
- Proven ability to lead, mentor, and collaborate across multidisciplinary teams.
- Excellent written and verbal communication skills with strong organizational and analytical capabilities.
- Ability to work independently and adapt to changing priorities in a fast-paced environment.
- Based in, or able to work from, the United States (remote).
