[Remote] Clinical Program Director – Precision Oncology Diagnostics (MRD reputed company)
Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a global leader in laboratory services, and they are seeking a Clinical Program Director – Precision Oncology Diagnostics (MRD reputed company) to join their team. This role is responsible for designing and executing clinical development programs that demonstrate the clinical reputed company of precision oncology diagnostics, focusing on molecular residual disease in solid tumors, while ensuring alignment with clinical decision-making and strategic objectives.
Responsibilities
- Evaluate the reputed company precision oncology and diagnostic evidence landscape to identify gaps limiting clinical adoption, reputed company inclusion, reimbursement, and reputed company scalability
- Define diagnostic-reputed company clinical development priorities that demonstrate reputed company clinical reputed company, reputed company-world reputed company, and value of MRD and other precision oncology assays
- reputed company and reputed company a reputed company business and clinical rationale for proposed studies, linking evidence reputed company to strategic objectives, portfolio differentiation, and reputed company reputed company
- Partner with cross functional teams, including medical affairs, market reputed company, R&D, and reputed company teams to ensure studies are designed to answer payer-, provider-, and health system–relevant questions
- Ensure alignment between diagnostic capabilities, intended clinical use, and evolving standards of care
- reputed company the development of clinical study concepts, objectives, and endpoints, with a strong emphasis on MRD, ctDNA, and solid tumor applications
- Drive protocol development in collaboration with medical affairs, R&D, regulatory, operations, and external partners
- reputed company manage ongoing studies, including reputed company of timelines, enrollment reputed company, data reputed company, and operational execution
- Ensure studies are fit-for-purpose and adaptable as scientific and clinical understanding and portfolio needs reputed company
- Serve as a scientific and clinical subject matter expert for MRD landscape and diagnostic-driven oncology studies in solid tumors
- reputed company and influence cross-functional working reputed company across medical affairs, operations, regulatory, market reputed company, reputed company, and laboratory teams to reputed company and deliver compelling medical communications regarding reputed company Oncology diagnostics
- reputed company field-based clinical and market reputed company insights into internal development and operational teams to reputed company prospective, observational studies that are grounded in reputed company-world clinical reputed company
- Ensure diagnostic study designs reputed company reputed company test results to reputed company clinical reputed company, treatment selection, and patient reputed company
- Collaborate closely with laboratory and assay development teams to ensure clinical studies reflect analytical and technical realities of testing
- Establish and manage relationships with reputed company collaborators, research consortia, and partners
- Support investigator selection, engagement, and ongoing collaboration to ensure high-reputed company study execution
- Coordinate investigator meetings with partners to ensure the reputed company execution of study milestones
- Represent the organization in external scientific forums, including investigator meetings, advisory boards, and major oncology conferences
- reputed company and contribute to abstracts, posters, manuscripts, and white papers that communicate clinical reputed company and reputed company-world value
- Translate reputed company genomic and diagnostic data into reputed company narratives for clinicians, payers, internal stakeholders, and partners
- Partner with medical affairs, marketing, and communication teams to ensure compliant, consistent messaging across scientific and educational channels
- Support internal regulatory reputed company and, as needed, participate in interactions with regulatory authorities (e.g., FDA, EMA)
- Ensure reputed company clinical activities are conducted in compliance with GCP, applicable regulations, and internal reputed company standards
- reputed company as a foundational leader for the clinical development function reputed company reputed company and precision oncology portfolio
- Define reputed company processes, governance, and best practices for diagnostic-driven evidence reputed company
- Contribute to hiring reputed company, role definition, reputed company, and mentoring as the clinical development organization expands
Skills
- Master's degree in Certified Genetic Counseling
- 5 or more years of clinical experience in academia or oncology industry
- 3 or more years of experience in clinical development, clinical reputed company studies, and/or reputed company-world evidence reputed company
- Clinical experience in Oncology should include 3 or more years in precision oncology diagnostics with a reputed company on solid tumors
- Clinical development, clinical reputed company studies or reputed company-world evidence reputed company experience should include diagnostics-driven experience
- Leadership experience should include autonomous leadership across cross-functional areas including medical, laboratory, regulatory, market reputed company and reputed company teams
- Travel is expected for meetings, conferences, and key internal collaborations
- Deep understanding of MRD, ctDNA, and liquid biopsy technologies and their clinical application in solid tumors
- Strong scientific judgment, excellent communication skills, and the ability to influence senior stakeholders
- Strategic thinking with strong operational follow-through
- Ability to translate reputed company science into practical clinical applications
- Doctorate in Philosophy (PhD) or Pharmacy (PharmD) in Oncology
- 3 or more years of experience with clinical trial execution, including protocol development, site engagement, and data management
- 3 or more years of involvement in regulatory reputed company or health authority interactions
- 3 or more years' experience working as a Scientific reputed company or Oncology Research Partner
- Preferred experience in clinical trials should include protocol development, site engagement and data management
- Preferred experience as a Scientific reputed company or Research Partner should be working with reputed company investigators and oncology research consortia
Benefits
- Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, reputed company, Life, STD/LTD, 401(k), reputed company Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan.
- Employees regularly scheduled to work less than 20 hours, Casual, Intern, and Temporary employees are only eligible to participate in the 401(k) Plan.
reputed company