Senior Scientist / Engineer: Advanced Oncology, Medical Devices, & Diagnost at Intertwine Associates

Mount Pleasant, South Carolina, United States -

Full Time

Start Date

Immediate

Expiry Date

03 Aug, 26

Salary

220000.0

Posted On

05 May, 26

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Oncology, Medical Device Development, Diagnostics, Biomedical Engineering, Nanotechnology, Artificial Intelligence, Complex Systems Modeling, Algorithm Development, Technical Writing, Data Analysis, Program Management, Regulatory Compliance, Cancer Biology, Biochemistry, Cell Biology, Mechanical Engineering

Industry

Business Consulting and Services

Description

Key Role Intertwine Associates is seeking a Senior Scientist / Engineer (Oncology / Medical Device Development) to support advanced research and development initiatives within the Advanced Research Projects Agency for Health (ARPA‑H). This role supports an ARPA‑H Program Manager leading ambitious, high‑risk, high‑reward programs focused on accelerating transformative health outcomes, particularly in oncology, diagnostics, and medical device innovation. In this role, you will collaborate closely with the Program Manager and broader government and performer teams to help design, evaluate, and execute complex R&D programs spanning medical device hardware and software, biomedical engineering, cancer biology, and translational diagnostics. The position is well suited for scientists and engineers who thrive in dynamic environments and enjoy translating deep technical insight into program‑level impact. Core Responsibilities Serve as a senior scientific and technical advisor to the Program Manager, supporting the development and execution of new and existing ARPA‑H R&D programs Conduct rigorous evaluations of the current scientific and technical landscape across oncology, diagnostics, and medical device development Identify gaps, risks, and opportunities within research portfolios aligned with ARPA‑H mission objectives Monitor and assess performer progress against defined technical milestones and quantitative performance metrics Critically review complex scientific, engineering, and technical data using strong logical and analytical reasoning Read, synthesize, and distill large volumes of information into concise, executive‑ready briefings for technical and non‑technical audiences Support program execution through documentation, internal reporting, and coordination across multidisciplinary teams Perform programmatic support tasks including data collection, analysis, and preparation of internal reports and briefings Operate effectively both independently and as part of an integrated team supporting ongoing ARPA‑H efforts Travel within CONUS (~10–35%) to support program reviews, meetings, and stakeholder engagements Basic Qualifications Minimum 8 years of industry, applied research, or medical‑institution experience (e.g., biotechnology, biopharmaceutical, medical device, or advanced technology organizations) Demonstrated experience spanning nanotechnology, advanced computation, algorithm development, artificial intelligence, or complex systems modeling Strong written and verbal communication skills, with the ability to clearly convey abstract or highly technical concepts Proven ability to synthesize large volumes of complex information into actionable, decision‑ready insights High level of professional curiosity and comfort operating in fast‑paced, high‑pressure R&D environments Proficiency with PowerPoint and Excel, including rapid development of materials during live discussions Ability to obtain and maintain a federal Public Trust Additional Qualifications (Preferred) PhD in biomedical sciences or engineering, with preference for oncology, cancer biology, biomedical engineering, biochemistry, cell biology, mechanical engineering, chemical engineering, or related fields Hands‑on experience with medical device and/or diagnostic development, including hardware and/or software components Familiarity with regulatory considerations in diagnostics or medical devices preferred Strong written and verbal communication skills, with the ability to convey complex concepts clearly and effectively Demonstrated ability to synthesize complex technical information into actionable insights Professional curiosity and a continuous drive to learn in fast‑paced, high‑impact R&D environments Proficiency with PowerPoint and Excel, including the ability to develop materials rapidly in high‑pressure meetings Ability to obtain and maintain a federal Public Trust Experience supporting senior leaders managing large or complex R&D portfolios Background spanning both basic and applied research Prior experience working with government agencies or federally funded R&D programs Experience bridging scientific discovery, product development, and program execution Intertwine Associates LLC – Equal Employment Opportunity Statement Intertwine Associates LLC is an Equal Opportunity Employer. We are committed to fostering a diverse and inclusive workplace where all individuals are treated with respect and dignity. Employment decisions are made without regard to race, color, religion, sex (including pregnancy, sexual orientation, and gender identity), national origin, age, disability, genetic information, veteran status, citizenship status, or any other characteristic protected by applicable law. Intertwine Associates LLC proudly supports U.S. Federal Government missions by providing exceptional technical talent and services. Certain roles may require U.S. citizenship or specific security clearances in accordance with federal contract requirements. The pay range for this role is: 90,000 - 220,000 USD per year (Remote (United States))

Responsibilities

Serve as a senior technical advisor to the ARPA-H Program Manager to design and execute high-risk R&D programs in oncology and medical devices. Responsibilities include evaluating the technical landscape, monitoring performer progress, and synthesizing complex data into executive briefings.