Director, Clinical Science

Responsibilities

• Design clinical study concepts with defined parameters and eligibility criteria
• Lead protocol design for oncology Signal Studies and portfolio development
• Author clinical study protocols and related documentation with cross-functional teams
• Deliver technical training on protocol validation to internal and external teams
• Create timelines and provide status updates on trial execution to senior leaders
• Conduct data reviews to ensure trial data integrity and compliance

Qualifications

• Advanced degree in Life Sciences (MD, PhD, PharmD, MS, RN, or equivalent scientific or clinical credential) required
• 10+ years of clinical development experience, particularly in oncology trials
• Expertise in oncology molecular diagnostics, including liquid biopsy metrics
• Demonstrated experience in clinical data review and trial protocol development
• In-depth knowledge of FDA regulations and Good Clinical Practice (GCP) guidelines
• Proven leadership in managing scientific personnel and cross-functional teams

Benefits

• Remote work flexibility within the USA
• Opportunity for international and domestic travel (up to 25%) for site management
• Access to collaborative work with cross-functional teams and leading experts
• Professional development and mentorship opportunities for junior staff
• Engagement in groundbreaking oncology diagnostics projects

Pay

$192,600 – $240,800 annually

Schedule

Remote work