[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, providing insights to enhance reputed company reputed company. They are seeking a Clinical Program Director to design and execute clinical development programs for precision oncology diagnostics, focusing on molecular residual disease in solid tumors.
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
- 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
Benefits
- Annual bonus under the reputed company Bonus Plan. Bonuses are payable based on corporate and/or business reputed company performance and are subject to individual performance modifiers.
- 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