The posting
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 Specialist in the Digital Health Sciences (DHS) team will provide scientific consultation to the commercial and project delivery teams. The Clinical Specialist will review clinical study protocols from prospective and current customers to identify the scientific and technological requirements of the clinical trial, and assist in identifying data collection methods and eCOA solution design based on best practices, patient and site preference, therapeutic area understanding, and regulatory guidance. The Clinical Specialist will also support senior DHS team members in preparing scientific content for pre-sales capabilities and bid defense presentations, while advising internal technical and operations teams to ensure clinical trials meet their objectives. This role offers the opportunity to develop deep expertise in COA/eCOA across multiple indications and stay at the forefront of industry trends and advances. KEY ACCOUNTABILITIES
Support the commercial team by analyzing study protocols and other relevant study documents and documenting study requirements Assist in the development of client-facing materials and content for strategic and commercial meetings Provide guidance on the development of eCOA solutions to internal study teams, ensuring solution design meets study objectives Understand product capabilities, functionalities, and suitability of solutions across different therapeutic indications Maintain knowledge of the most recent industry best practices and regulatory requirements for clinical outcome assessments (COA) Conduct literature searches and reviews to develop therapeutic area knowledge Participate in thought leadership efforts to demonstrate the company's scientific expertise internally and externally Manage time effectively across multiple concurrent projects
KNOWLEDGE, SKILLS & ATTRIBUTES Essential:
Advanced degree (MSc or PhD) in biological science or healthcare Good understanding of clinical research and the drug development cycle Proven ability to multitask, manage time effectively, and deliver in a fast-paced environment Business-driven mindset with an understanding of commercial drivers and growth objectives Experience presenting scientific content to diverse audiences Comfortable developing expertise in new fields through research and networking Proven ability to be an effective, positive team player who can work across teams and in a matrix environment Strong interpersonal and communication skills; ability to engage with stakeholders from a range of disciplines Excellent written and verbal English communication skills
Desirable:
Prior experience in clinical research, preferably across more than one therapeutic area or indication Ability to communicate effectively with clients and all levels within the organization Prior experience with patient-reported outcome measures (PROs) or Clinical Outcome Assessments (COAs)
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. #LI-SR1
