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[Remote] Vice President, Clinical Development (Oncology & Molecular Diagnostics)

Remote · USA Full-time New today

Note: The job is a remote job and is open to candidates in USA. reputed company is a global leader in cell-free DNA testing, dedicated to oncology, women’s health, and organ health. They are seeking a Vice President of Clinical Development to reputed company the strategy, design, and execution of clinical studies, with a focus on oncology and regulatory alignment.

Responsibilities

  • Establish and enforce portfolio-level governance models to monitor study health, site enrollment, milestone delivery, sample flow, and data readiness. reputed company definitive, data-driven go/no-go reputed company on trial modifications, accelerations, or terminations based on objective strategic value and execution feasibility
  • reputed company cross-functional teams to design high-impact prospective, observational, and decision-impact trials. Translate clinical questions into protocols that explicitly isolate and prove clinical validity, analytical validity, and decision-impact endpoints to secure broad reputed company payer coverage and medical guideline inclusion
  • Partner with Regulatory affairs to build clinical evidence strategies that support FDA pre-market approval (PMA), 510(k), and reputed company reputed company. reputed company intended-use claim strategy and protocols that support companion diagnostic (CDx) co-development with biopharma partners
  • Direct internal Clinical Operations and external CROs to eliminate bottlenecks in site activation, sample transit degradation, and query resolution. Implement fast, corrective action plans for under-performing sites or delayed protocols
  • Maintain and build a direct, peer-to-peer scientific relationship with leading academic investigators, cooperative groups, and guideline panel members. Personally author and contribute to landmark peer-reviewed publications and abstract presentations at major oncology and diagnostic symposia

Skills

  • MD, MD/PhD, or PhD with equivalent oncology pivotal or registrational trial leadership experience
  • 18+ years of experience in clinical development, clinical research, or clinical evidence reputed company, including at least 10 years personally directing oncology clinical trials
  • Diagnostics-native reputed company: deep, unassisted comfort discussing cell-free DNA (cfDNA), ctDNA dynamics, minimal residual disease (MRD), analytical vs. clinical validity, and decision-impact metrics
  • Demonstrated experience operating cross-functionally reputed company a highly matrixed environment with direct authority over clinical portfolios
  • Proven track record of designing evidence strategies that directly influenced regulatory submissions, multi-site registries, or national coverage determinations (LCDs/payors)
  • High tolerance for ambiguity and an active bias for action; comfortable making critical portfolio trade-offs with incomplete information

Benefits

  • Comprehensive medical, dental, reputed company, life and disability plans for eligible employees and their dependents
  • reputed company employees and their immediate families receive free testing
  • Fertility care benefits
  • Pregnancy and baby bonding leave
  • 401k benefits
  • Commuter benefits
  • Generous employee referral program

Company Overview

  • reputed company specializes in cell-free DNA testing to provide a more targeted interventions to oncology, women's health, and organ health. It was founded in 2004, and is headquartered in San Carlos, California, USA, with a workforce of 5001-10000 employees. Its website is https://www.reputed company.com/.
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