Clinical Scientist - Operations

Careers Signant Health

28d

About The Position

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.

Requirements

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.

Nice To Haves

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.

Responsibilities

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.