Jobs in the United States

25+ jobs

Save this search

Added 2 mins ago
Director of Event Planning
Marriott
HOUSTON, TX
…of responsibility is the event planning team, including the Senior Event Managers, Event Managers, Associate Event Managers and Administrative Assistants. Position oversees the…
Added 3 mins ago
Biomedical Technician
BPA USA Bio-Med Appl of Pennsylvania
Youngstown, OH
…Technician role as well as a leadership path from Area Technical Operations Manager, Regional Technical Operations Manager, and Senior Director Technical Services, overseen by a Vice…
Added 9 mins ago
Specialist, Project Management, Bergdorf Goodman
Saks
New York, NY
…overseeing creative requests for homepage, email, narratives, sales associate emails, print and omni projects. Part of a team of project managers, reporting to the Senior Project Manager,…
Added 9 mins ago
Sr. Manager, People Business Partner
Saks
Los Angeles, CA
The Senior Manager, People Business Partner – West Region serves as a strategic People partner to store and regional leadership across Neiman Marcus and Saks Fifth Avenue. This role…
Added 11 mins ago
Director, Sr. Counsel - Functional Support
RTX
United States
…problems. With our three market leading businesses, world-class operations and investments in research and development, we offer capabilities and opportunity no one else can. Together, we…
Added 18 mins ago
CF
Part-Time Clinical Leader - Gilroy
Center for Social Dynamics
Gilroy, CA
- $35 to $43 USD / hour
- Part-time
Career Compass: A clearly defined pathway supporting clinical mastery, BCBA progression, and leadership development
Added 19 mins ago
Industrial Engineer 2
Sysco Payroll, Division of Sysco Resources Services, LLC
United States
Responsible for managing the development and maintenance of engineered labor standards for the operations departments at Sysco Sites and other Functional/Business Units through engineered…
Added 20 mins ago
OC
Lieutenant - Corrections (Support Operations and Training)
Osceola County
Kissimmee, FL
- $39.96 USD / hour
…overseeing and ensuring the efficiency and effectiveness of facility operations. The employee works with considerable independence in the performance of regularly assigned duties; however,…
Added 24 mins ago
Associate Director (Scientific Data and Publications)
GlaxoSmithKline LLC
Upper Providence, PA
Added 24 mins ago
P
Associate Director, Group Lead, Data Management Reporting and Analytics
Pfizer
Collegeville, PA
- $111,900 to $207,400 USD / year
Understanding of the drug development process and data operations required for the reporting of clinical trial data
Added 42 mins ago
Senior Associate, Infrastructure Engineer
KPMG LLP
McLean, VA · Washington, DC
KPMG is currently seeking a Senior Associate, Infrastructure Engineer to join our Federal Services organization.
Added 43 mins ago
BAI – Senior Manager, US Forecasting, Oncology
Amgen USA Inc.
CA · Deerfield, IL
…insights crucial for driving commercial success. As a Forecasting Senior Manager, you will contribute significantly to our inline brand strategy, executing and managing discussions with…
Added 44 mins ago
Associate Deputy Chief, Marketing, Digital Strategy and Enrollment Growth
Dallas College
United States
Dallas College is seeking an accomplished, forward-thinking marketing executive to serve as Associate Deputy Chief, Marketing, Digital Strategy and Enrollment Growth.
Added 50 mins ago
NJ
Senior AI Technical System Analyst (Information Technology Analyst 3)
New Jersey Courts
Trenton, NJ
- $94,668.29 to $133,073.24 USD / year
The New Jersey Judiciary Information Technology Office, a recognized leader in the development of applications that improve the operations and efficiency of the courts and deliver…
Added 51 mins ago
Operations Support Senior Associate - El Segundo, CA
Military Spouse Jobs & VetJobs
United States
Provides basic technical and systems support under the direction of more senior level Operations Support Engineers, and identifies opportunities for basic process improvements. Assists in…
Added 54 mins ago
2027 Summer Intern: Associate Billing Solutions Analyst (Customer Operations)
Spectrum
Charlotte, NC
In addition to role-specific projects, you’ll take part in professional development sessions, networking opportunities, mentorship and experiences that help you grow personally and…
Added 59 mins ago
Senior Manager, Technical Operations
E.R. Squibb & Sons,L.L.C.
Princeton, NJ
The Senior Manager, Technical Operations manages the daily operations of one or more animal facilities and specialty areas, including areas supporting USDA-regulated species, infectious…
Added 59 mins ago
Senior Specialist, Manufacturing NPI & Clinical Readiness
JuN - Seattle Dexter
Bothell, WA
The Senior Specialist partners closely with Manufacturing Operations, MSAT, Quality, IT/MES, Engineering, and Supply Chain to support technical transfer, manufacturing readiness, and…
Added 1 hour ago
Sr. Manufacturing Associate, cGMP Manufacturing
Sumitomo Pharma America, Inc
Morrisville, NC
The Senior Manufacturing Associate (Sr. MA) is a key contributor within the cGMP Manufacturing organization and plays a critical role in supporting Sumitomo Pharma America (SMPA) by…
Added 1 hour ago
UO
Access Associate Senior - Children's
University of Virginia
Charlottesville, VA
- $19.5 to $33.94 USD / hour
Make a meaningful impact on the front line of patient access and experience. As an Access Associate Senior at UVA Health, you play a critical role in ensuring patients receive seamless,…
Added 1 hour ago
Academy Director $5,000 Sign-On Bonus + Excellent Benefits
Brightside Academy
Philadelphia, PA
Career Advancement Opportunities – Pathways to senior and regional leadership
Added 1 hour ago
HH
Senior Care Coordinator
Hinge Health
Remote, United States
- $36.32 to $54.48 USD / hour
Helping members navigate healthcare starts with clear guidance and support at each step of their care journey. As a Senior Flex Care Coordinator on Hinge Health’s Clinical Operations team,…
Added 1 hour ago
Biomedical Technician
Fresenius Medical Care
Youngstown, OH
…Technician role as well as a leadership path from Area Technical Operations Manager, Regional Technical Operations Manager, and Senior Director Technical Services, overseen by a Vice…
Added 1 hour ago
District Sales Manager - Dallas/Ft Worth SE, TX
Mattress Firm, Inc
Dallas, TX
Reviews performance and provides development of each associate
Added 1 hour ago
B57 Prep-Tank Technician
(2605) Sanofi Vaccines US Inc.
Swiftwater, PA
Works with senior technicians and managers to ensure continuous, adequately staffed operations

Natera

Associate Director, Strategic Program Management

Remote, United States

$150,300 - $195,150 USD

Apply About employer

Applications open in a new tab.

Job details

Pay: $150,300 - $195,150 USD
Experience: 10+ years of progressive program or project management experience in molecular diagnostics, in vitro diagnostics, medical devices, biotechnology, or a related regulated field.
Posting language: English
Posted: Nov 2, 2026

Original job description

Associate Director, Strategic Program Management, CDx/IVD

Position Overview

Natera is seeking an Associate Director of Strategic Program Management to lead IVD and companion diagnostic (CDx) programs from development planning through PMA submission. This leader will shape the development strategy with functional experts and own the integrated execution plan across assay development, software and bioinformatics, analytical and clinical validation, laboratory operations, Quality, and Regulatory Affairs.

The Associate Director will bring clarity to complex programs, connect decisions across workstreams, and drive teams toward critical development and submission milestones. This is a highly visible role requiring the ability to lead without direct authority, resolve competing priorities, and present clear recommendations to the Executive Leadership Team (ELT). The role focuses on internal CDx development and execution; dedicated partnership leaders own external pharmaceutical partner management.

Primary Responsibilities

Lead IVD/CDx program execution

Lead complex IVD/CDx programs through development, design transfer, validation, and PMA submission.
Build and maintain an integrated program plan covering deliverables, resources, dependencies, decision points, and regulatory milestones.
Partner with functional leaders to define objectives, development priorities, success criteria, and executable plans.
Anticipate risks, identify gaps and trade-offs, and drive timely decisions across functions.
Establish clear program governance, ownership, escalation paths, and accountability for commitments.

Drive development and submission readiness

Integrate assay development, design controls, software and bioinformatics, analytical validation, clinical validation, laboratory implementation, and submission activities.
Partner with Regulatory Affairs and Quality to align program execution with FDA interactions, applicable requirements, and PMA evidence needs.
Coordinate plans for assay changes, comparability or bridging studies, and transition to the final CDx configuration, as applicable.
Lead reviews at major development gates to confirm deliverables, readiness criteria, open risks, and decisions.
Track submission-critical evidence and documentation, and drive resolution of gaps that could affect PMA quality or timing.

Provide executive leadership and communication

Present program strategy, progress, risks, trade-offs, and recommendations to the ELT and other senior governance forums.
Translate complex scientific, operational, and regulatory issues into concise, data-backed options and decisions.
Build alignment among leaders with different priorities and hold teams accountable for agreed actions and milestones.
Escalate material issues early, with a clear assessment of their impact and a recommended path forward.
Provide the internal program status and decision support needed by colleagues who lead external pharmaceutical partner relationships.

Qualifications

Required

Bachelor’s degree in life sciences, engineering, or a related field, or equivalent relevant experience.
10+ years of progressive program or project management experience in molecular diagnostics, in vitro diagnostics, medical devices, biotechnology, or a related regulated field.
Direct experience leading CDx or IVD development programs involving design controls, validation planning, and FDA submission preparation.
Experience building and driving integrated plans across technical, clinical, regulatory, quality, software, and operations functions.
Demonstrated ability to lead senior cross-functional stakeholders, resolve competing priorities, and deliver results without direct reporting authority.
Experience presenting complex programs, risks, and recommendations to executive leadership.
Strong ability to connect technical decisions, resource needs, regulatory evidence, and timelines to the overall program strategy.

Preferred

Experience leading a CDx or IVD program through PMA submission or a major PMA milestone.
Experience with next generation sequencing, genomic diagnostics, or biomarker-defined patient populations.
Experience coordinating analytical and clinical validation strategies and managing changes between clinical trial and final commercial assay configurations.
Familiarity with pharmaceutical development timelines and the dependencies between a therapeutic program and its companion diagnostic.
Advanced degree or program management certification.

Leadership Expectations

The successful candidate will lead the program beyond milestone tracking. They will understand the science and regulatory strategy well enough to ask informed questions, recognize when a decision in one workstream creates risk elsewhere, and bring the right leaders together to resolve it. They will foster trust and open discussion, make ownership clear, and give executives an accurate view of progress and the decisions needed to deliver the program.

The pay range is listed and actual compensation packages are based on a wide array of factors unique to each candidate, including but not limited to skill set, years & depth of experience, certifications and specific office location. This may differ in other locations due to cost of labor considerations. Remote USA

$150,300 - $195,150 USD

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.

WHAT WE OFFER

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!

For more information, visit www.natera.com.

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.

If you are based in California, we encourage you to read this important information for California residents.

Link: https://www.natera.com/notice-of-data-collection-california-residents/

Please be advised that Natera will reach out to candidates with a @natera.com email domain ONLY. Email communications from all other domain names are not from Natera or its employees and are fraudulent. Natera does not request interviews via text messages and does not ask for personal information until a candidate has engaged with the company and has spoken to a recruiter and the hiring team. Natera takes cyber crimes seriously, and will collaborate with law enforcement authorities to prosecute any related cyber crimes.

For more information:

BBB announcement on job scams
FBI Cyber Crime resource page

Apply About employer

Report this job