Senior Clinical Trial Design And Development Manager

Summary

Join Natera as a Senior Clinical Scientist/Clinical Development Manager and contribute to our innovative molecular therapeutics efforts. This role blends scientific expertise in clinical trials with strong program management skills to lead the development and execution of clinical studies. You will design clinical trial protocols, oversee implementation, collaborate with cross-functional teams, manage timelines and budgets, and ensure regulatory compliance. The position requires an advanced degree in a life science field (Ph.D. preferred) and proven experience in clinical trial design and management, particularly in oncology or personalized medicine. Natera offers a competitive salary, comprehensive benefits, and a collaborative work environment.

Requirements

• Advanced degree in a life sciences or related field (Ph.D. preferred)
• Proven experience in clinical trial design and management, particularly in oncology or personalized medicine
• Strong understanding of regulatory requirements and clinical development stages
• Excellent project management skills with a proven track record of leading cross-functional teams
• Ability to communicate effectively with a variety of stakeholders including scientific and non-scientific audiences
• Detail-oriented with strong analytical and problem-solving skills

Responsibilities

• Design clinical trial protocols
• Oversee the implementation of clinical trials, ensuring they adhere to scientific standards, regulatory requirements, and ethical guidelines
• Collaborate with biostatisticians to ensure appropriate data analysis methodologies are employed
• Monitor trial progress, analyze interim results, and prepare reports for regulatory submissions
• Contribute to core clinical documents: clinical development plan, target patient profile, site training materials
• Develop and maintain a comprehensive program plan that encompasses all aspects of the clinical trial lifecycle from inception through completion
• Coordinate cross-functional teams across clinical operations, regulatory affairs, and other departments to ensure alignment and effective execution of the program
• Manage timelines, resources, and budgets to ensure project milestones are met on schedule and within budget
• Identify risks and implement risk management strategies to mitigate potential impacts on the program
• Develop content and reports for advisory boards, steering committees, internal and external training decks
• Serve as the primary point of contact for all program-related communications, including updates to senior management and external partners
• Build and maintain relationships with clinical site teams, external CROs, and other stakeholders
• Ensure transparent communication across all levels of the project team and stakeholders
• Ensure all clinical trial activities comply with regulatory standards and ethical practices
• Prepare documentation and support regulatory submissions and interactions
• Stay updated with changes in regulatory requirements and industry standards

Preferred Qualifications

Ph.D

Benefits

• Comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents
• Natera employees and their immediate families receive free testing in addition to fertility care benefits
• Pregnancy and baby bonding leave
• 401k benefits
• Commuter benefits
• Generous employee referral program