Associate Director, Clinical Science US Remote

Natera is seeking a highly motivated and experienced Clinical Scientist to support the development and execution of our innovative Oncology programs. The Associate Director, Clinical Science will ensure the successful execution of clinical development programs and deliverables in partnership across the organization, with external vendors, and with external academicians and collaboration partners. The Associate Director, Clinical Science will be accountable to jointly develop clinical program strategy and work collaboratively with other functional representatives to assure that activities are executed within expected scope, compliance, budget, and timelines. Specifically, the candidate will work closely with colleagues cross‑functionally in clinical development, clinical operations, data management safety/pharmacovigilance, regulatory, biostatistics, translational medicine, and program leadership. Primary Responsibilities Develop study concepts, including study design, schedule of assessments, objectives/endpoints, and eligibility criteria Collaborate cross‑functionally to develop Protocol and ICF documents / amendments and present these to governance committee and early clinical development team meetings as required Provide protocol training and contribute to CRF design Ensure study manuals align with protocol and engage investigators in study design Seek input from key investigators on study design and methodology to ensure alignment with research objectives, and actively participate in pre‑site selection discussions, site initiation visits, and investigator meetings to support successful study execution Contribute to and oversee real‑time clinical data reviews (including oversight of CROs when applicable) Serve as a clinical science representative on internal and external meetings Develop clinical project execution timelines and provide status updates to senior management to ensure the timely delivery of program milestones In collaboration with Data Management will develop Data Review Plan, and monitor clinical data for specific trends, ensure CRF design adequately supports data collection in alignment with the protocol in collaboration with Data Management/Programming Support meetings (advisory boards, etc) and deliver presentations Drive clinical research plans, including company and investigator‑initiated studies Effectively interact with senior members in other functional areas for strategic planning to ensure optimized clinical development in accordance with corporate objectives Build relationships with KOLs, consortiums, and sites Provide scientific input into design & implementation of clinical trial(s), their delivery, clinical data review and data cleaning, interpretation of results, reporting successfully on time, and activities required for registration of the product As appropriate, participates in ongoing enhancements/development of team processes, structures, systems, tools, and other resources; As appropriate, coaches and guides less experienced Clinical Scientists Manage one or more direct reports including being responsible for hiring, training, developing, and retaining talent on staff, as needed As appropriate, participates in competitive intelligence and/or other market/industry assessment activities and projects Maintains scientific and clinical knowledge in the specific therapeutic and disease area(s) of assignment Ensure HIPAA/PHI compliance and maintain training requirements Perform other duties as assigned Qualifications Advanced degree in Life Sciences (MD, PhD, Pharm D, MS, RN or similar scientific field) preferred 8+ years pharma/biotech industry experience in clinical development in oncology clinical trials Deep understanding and preferably experience in oncology molecular diagnostics, oncology companion diagnostics or early cancer detection Experience in data review, data cleaning, managing and interpreting clinical trials results as well in writing clinical trial protocols Possesses sound foundational knowledge of FDA and other major country regulations and detailed knowledge of Good Clinical Practice other regulations governing clinical research Experience with managing direct reports, ensuring that roles are performed in accordance with job descriptions and that training is conducted and maintained appropriately Knowledge, Skills, and Abilities Problem‑solving skills and a fast learner Strong communication (oral and written) and attention to detail Ability to work independently and collaboratively Analytical and creative thinking Familiarity with Google and Microsoft suites Desire to work in a dynamic environment Hands‑on leadership and a strong work ethic Ability to apply business knowledge, exercise judgment, and elevate issues appropriately Strong project management, organizational, and interpersonal skills Adaptability, initiative, and team‑building skills Demonstrated success in working in a cross‑functional environment Successful and superior influencing skills across all levels of the organization and external collaborators Conflict resolution and follow‑through skills Results and goal‑oriented Strategic and flexible thinking Physical Demands & Work Environment Office or home office setting with internet access Ability to use a computer, phone, and read materials Flexibility to work with colleagues in a global setting Able to engage in work‑related travel up to 25% Our Opportunity Natera™ is a global leader in cell‑free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives. The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world‑class institutions, who care deeply for our work and each other. When you join Natera, you’ll work hard and grow quickly. Working alongside the elite of the industry, you’ll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management. Benefits Competitive Benefits – Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much more. We also offer a generous employee referral program! Remote USA $174,700 - $218,400 USD If you are based in California, we encourage you to read this important information for California residents. Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives. Inclusive collaboration benefits our employees, our community and our patients, and is critical to our mission of changing the management of disease worldwide. All qualified applicants are encouraged to apply, and will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, veteran status, disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories, consistent with applicable laws. #J-18808-Ljbffr