Director, Clinical Science

Accountabilities:

• Lead the design and development of oncology clinical study concepts, including endpoints, eligibility criteria, schedules of assessments, and overall study structure

• Collaborate cross-functionally to develop protocols, informed consent forms, amendments, and other key clinical trial documents

• Provide scientific and operational input into clinical trial execution, ensuring alignment with study objectives, timelines, and regulatory standards

• Partner with clinical operations and data management to oversee real-time data review, quality control, and data cleaning processes

• Develop and maintain clinical project timelines, ensuring transparent communication of progress, risks, and milestones to senior leadership

• Engage with investigators, key opinion leaders, and external partners to support study design, site selection, and trial execution

• Contribute to clinical data interpretation, reporting, and preparation of study results for internal and external dissemination

• Support business and investigator-initiated research programs aligned with broader oncology strategy

• Participate in advisory boards, scientific meetings, and external collaborations to support clinical development efforts

• Ensure compliance with HIPAA, GCP, and applicable regulatory requirements across all clinical activities

• Provide mentorship and guidance to junior clinical scientists and contribute to team capability building when needed

Requirements:

• Advanced degree in Life Sciences required (MD, PhD, PharmD, MS, RN, or equivalent scientific discipline strongly preferred)

• 10+ years of experience in pharmaceutical, biotech, or clinical research environments with a focus on oncology clinical trials

• Strong expertise in clinical development, including protocol design, data review, and clinical trial execution

• Deep understanding of oncology, molecular diagnostics, or companion diagnostics; experience in early cancer detection strongly preferred

• Solid knowledge of FDA regulations, ICH-GCP guidelines, and global clinical research standards

• Experience working in cross-functional teams across clinical operations, data management, regulatory, and biostatistics

• Proven ability to interpret complex clinical data and translate insights into actionable development decisions

• Strong communication, presentation, and scientific writing skills

• Demonstrated ability to manage multiple priorities in fast-paced, matrixed environments

• Leadership experience, including mentoring or managing direct reports, is highly preferred

• Strong analytical thinking, attention to detail, and problem-solving capabilities

• Ability to build relationships with external stakeholders, including investigators and academic partners

Benefits:

• Competitive annual salary range: $192,600 – $240,800 USD, based on experience and qualifications

• Comprehensive medical, dental, and vision insurance coverage

• Life, disability, and retirement savings benefits

• Performance-based compensation opportunities where applicable

• Fertility, pregnancy, and family support benefits

• Paid time off, including vacation, sick leave, and parental bonding leave

• Remote-first work flexibility across the United States

• Opportunity to contribute to cutting-edge oncology and genetic innovation programs

• Career growth within a globally recognized leader in precision medicine

• Inclusive, science-driven culture focused on improving patient outcomes worldwide.

How Jobgether works:
We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team.
We appreciate your interest and wish you the best!
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