Director, Clinical Science

1 hour, 18 minutes ago
Full-time
Lead
Project and Program Management
Natera

Natera

Natera specializes in cell-free DNA testing, providing advanced genetic testing services for oncology, women's health, and organ health to help families diagnose and manage genetic diseases.

Pharmaceuticals
1K-5K
Founded 2004

Description

  • Develop study concepts, including study design, schedule of assessments, objectives/endpoints, and eligibility criteria.
  • Collaborate cross-functionally to create protocols, informed consent documents, and amendments for governance and early clinical development review.
  • Provide protocol training and contribute to CRF design and study manual alignment.
  • Engage investigators, KOLs, consortiums, and sites to support study design, methodology, site selection, and execution.
  • Oversee real-time clinical data review, data cleaning, and CRO oversight when applicable.
  • Develop clinical project execution timelines and provide status updates to senior management on program milestones.
  • Work with Data Management and Programming to develop data review plans and ensure data collection aligns with the protocol.
  • Support advisory boards, internal/external meetings, and presentations.
  • Drive clinical research plans, including company-sponsored and investigator-initiated studies, and support registration-related activities.
  • Manage one or more direct reports, including hiring, training, developing, and retaining staff, as needed.

Requirements

  • Advanced degree in Life Sciences such as MD, PhD, PharmD, MS, RN, or a similar scientific field preferred.
  • 10+ years of pharma/biotech industry experience in clinical development within oncology clinical trials.
  • Deep understanding of oncology molecular diagnostics, oncology companion diagnostics, or early cancer detection, preferred.
  • Experience in data review, data cleaning, interpreting clinical trial results, and writing clinical trial protocols.
  • Sound foundational knowledge of FDA and other major country regulations, plus detailed knowledge of Good Clinical Practice and other clinical research regulations.
  • Experience managing direct reports and ensuring appropriate training and performance expectations are met.
  • Strong communication skills, both oral and written, with attention to detail.
  • Ability to work independently and collaboratively in a cross-functional environment.
  • Familiarity with Google and Microsoft suites.
  • Ability to travel up to 25% and work in an office or home-office setting with internet access.

Benefits

  • Remote USA pay range of $192,600 to $240,800 USD.
  • Comprehensive medical, dental, vision, life, and disability insurance for eligible employees and dependents.
  • Free testing for employees and their immediate families.
  • Fertility care benefits.
  • Pregnancy and baby bonding leave.
  • 401(k) benefits.
  • Commuter benefits.
  • Generous employee referral program.

Interested in this position?

Apply directly on the company website

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