Associate Director, Clinical Science

About the role

This role will support clinical priorities focused on quality, patient-centered outcomes, and effective care delivery. You will collaborate with clinical leaders, operational teams, and cross-functional stakeholders to improve standards, workflows, and execution. The position offers the opportunity to strengthen care quality, team performance, and measurable outcomes within a life sciences environment.

Responsibilities

• Design clinical study protocols for oncology biobanking
• Lead protocol development and clinical activities for biospecimen studies
• Collaborate to author clinical study documents and technical amendments
• Conduct protocol validation training for internal teams and CROs
• Ensure study manuals align with protocol specifications
• Manage timelines and deliver status updates to senior leadership
• Lead data review processes for clinical datasets

Qualifications

• Advanced degree in Life Sciences (PhD, MD, PharmD, MS, RN, or equivalent) required
• 8+ years of clinical development experience in oncology trials
• Expertise in oncology molecular diagnostics and biospecimen repository frameworks
• Proven experience in clinical data review and protocol development
• Knowledge of FDA regulations, IVD standards, and GCP guidelines
• Experience managing scientific staff in a clinical trial environment

Benefits

• Mentoring opportunities for junior staff
• Potential for career growth within a dynamic clinical environment
• Participation in pioneering oncology diagnostic initiatives
• Flexible work environment enabling remote office capabilities
• Support for professional development and continuous learning