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Associate Director, Clinical Development

2 days, 13 hours ago
United States
Full-time
Lead
Program Manager
Project and Program Management
HIPAA
Apply Now
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
View All Jobs 74

Description

  • Drive the design and timely execution of clinical research plans, including clinical studies, investigator-initiated studies, and research projects.
  • Build and maintain relationships with KOLs, consortiums, clinical site staff, and external partners to address data gaps.
  • Develop clinical project timelines and provide status updates to senior management on program milestones.
  • Lead contracting and budget approval activities with academic centers and community practices participating in research studies.
  • Participate in due diligence activities to evaluate external opportunities that support business objectives.
  • Collaborate with senior leaders across functions to support strategic planning and clinical development aligned with corporate objectives.
  • Lead project resource planning, reforecasting, and program milestone management.
  • Manage and develop a team of approximately 3-6 employees, including staffing, coaching, training, and hiring.
  • Ensure employees comply with study requirements, company policies, and applicable regulations.
  • Promote a positive, equitable, and collaborative work environment while driving goals and organizational change.

Requirements

  • B.S. degree in a relevant scientific discipline or related field; advanced degree preferred.
  • 8+ years of clinical research experience, including 3-5 years in a clinical research leadership role.
  • Established experience managing staff and setting department objectives.
  • Knowledge of applicable regulations and GCPs governing clinical trials.
  • Current training in Good Clinical Practice (GCP) is required.
  • Experience and knowledge of oncology is a plus.
  • Experience with regulated in vitro diagnostics is a plus.
  • Strong project management, organizational, and communication skills.
  • Proficiency in MS Word, Excel, PowerPoint, and clinical trial databases.
  • Ability and willingness to travel with minimal advance notice.
  • Must complete HIPAA/PHI, policy compliance, and security training within the first 30 days of hire.
  • Must pass a post-offer criminal background check.

Benefits

  • Remote USA role with a listed salary range of $144,900 to $181,100 USD.
  • Comprehensive medical, dental, vision, life, and disability coverage 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.
  • Employee referral program.

Interested in this position?

Apply directly on the company website

Apply Now

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