Clinical Scientist - Operations

About Signant Health

At Signant Health, we help bring life-changing treatments to patients faster. We are a global evidence generation company that supports clinical trials with smart technology, scientific expertise, and hands-on operational support — so better data leads to better decisions in healthcare. We embrace AI and advanced technologies to enhance every aspect of what we do, from data analysis to operational efficiency.

Our teams work at the intersection of science, technology, and patient experience, delivering digital solutions powered by AI innovation that make clinical trials more efficient, more accurate, and more accessible around the world. Trusted by leading pharmaceutical companies and CROs, our platforms and services support studies across more than 90 countries and have contributed to hundreds of new drug approvals.

If you are motivated by meaningful work, global impact, and innovation in clinical research and digital health — including the opportunity to work with cutting-edge AI technologies — you will find purpose and opportunity at Signant Health.

About the Role

The Clinical Scientist is a member of the Digital Health Sciences team and serves as a scientific resource for internal and external stakeholders on the use of eCOA and other digital health technologies — including eConsent and sensors/wearables — in clinical trials. This role supports the full lifecycle of commercial and scientific activity: reviewing study protocols to identify requirements, advising on solution design, contributing to pre-sales and bid defense meetings, and providing input to product development and marketing initiatives. The Clinical Scientist also drives thought leadership through research, industry participation, and client-facing scientific consultation.

Key Accountabilities

• -Support the commercial team by analyzing study protocols and relevant study documents, documenting requirements, and presenting scientific content in client meetings.
• -Advise technical, operations, and client teams on the development of eCOA solutions to ensure solution design meets clinical trial objectives.
• -Provide consultation services through special projects addressing client-specific scientific requests or external initiatives.
• -Maintain comprehensive knowledge of current industry best practices and regulatory requirements for clinical outcome assessments (COA).
• -Stay at the leading edge of eCOA and digital health technologies through participation in industry forums, working groups, and collaboration with clients and Key Opinion Leaders.
• -Develop thought leadership materials and scientific content that demonstrate the company's expertise internally and externally.
• -Represent Signant Health in the industry through active participation in forums, conferences, webinars, and publications.
• -Manage time effectively across multiple concurrent projects.
• -Develop training and marketing materials in support of organizational initiatives.

Knowledge, Skills & Attributes

Essential:

• -Advanced degree (PhD preferred) in biological science or a healthcare-related field.
• -1–3 years of experience in clinical trial technology or a related industry, preferably in a client-facing role.
• -In-depth understanding of clinical research and the drug development cycle.
• -Knowledge of clinical outcome assessments (COA) and related science, and/or eConsent, EDC, sensors, and wearables.
• -Proven ability to multitask, manage time effectively, and deliver in a fast-paced environment.
• -Business-driven mindset with an understanding of commercial growth.
• -Familiarity with the intersection of technology and science in digital health for clinical trials.
• -Proven ability to collaborate effectively across teams and in a matrix environment.
• -Ability to develop expertise in new fields through independent research and networking.
• -Excellent written and spoken English communication skills.

Desirable:

• -Prior experience in commercial pre-award activities such as capabilities presentations, bid defense meetings, and/or solution design and requirements gathering.
• -Experience in the development and use of ePRO or eCOA solutions for clinical trials.
• -Ability to communicate effectively with clients and across all levels of the organization.

Why Signant Health?

At Signant Health, your work has real impact. Everything we build, support, and deliver helps advance clinical research and bring new treatments to patients faster — improving lives around the world. Our teams combine science, technology, and operational expertise to solve complex clinical trial challenges, and every role contributes to that mission.

We offer a collaborative, global environment where you can grow your career while working alongside experts across clinical, technology, data, and operations, with opportunities to learn, take ownership, and drive meaningful innovation — not just maintain the status quo.

If you are looking for purpose-driven work, smart colleagues, and the opportunity to help shape the future of clinical research and digital health, Signant Health is the place to do it.

At Signant Health, accepting difference isn't enough — we celebrate it, we support it, and we nurture it for the benefit of our team members, our clients, and our community. We are proud to be an equal opportunity workplace and an affirmative action employer, committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, or veteran status. Prior to their start date, all new hires are required to be verified through a thorough background check and identity verification to confirm eligibility for employment.

Unsolicited resumes submitted by agencies or third-party recruiters directly to hiring managers or any Signant Health employee will not be considered and will not obligate Signant Health to any fees or terms associated with the submission.

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