This could be the Opportunity of Your Life!
Signant Health is a global evidence generation company. We’re helping our customers digitally enable their clinical trial programs, meeting patients where they are, driving change through technology and innovations and reimagining the path to proof.
Working at Signant Health puts you in the very heart of the world’s most exciting sector - a high-growth, dynamic company in an extraordinary industry.
Where do you fit in?
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.
• Will assist in identifying the data collection methods and eCOA solution design based on best practices, patient/site preference, understanding of the therapeutic area, and regulatory guidance.
• Will also support senior DHS team members in preparing scientific content for pre-sales capabilities, and bid defense presentations.
• Will support the development of eCOA solutions, advising internal technical and operations teams, ensuring clinical trials meet their objectives. They will develop expertise in COA/eCOA across different indications, as well as an understanding of industry trends and advances.
As part of our team, your main responsibilities will be to:
• Support the commercial team by analyzing study protocols and other relevant study documents, 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 the 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 search and review to develop therapeutic area knowledge.
• Participate in thought leadership efforts to demonstrate the company’s scientific expertise internally and externally.
• Manage time across multiple concurrent projects.
What You'll Bring:
• Advanced degree (MSc) in biological science or healthcare.
• Good understanding of clinical research and the drug development cycle.
• Proven ability to multitasking, time management and task-oriented performance able to work in a fast-paced environment.
• Business driven and business growth savvy.
• Experience presenting scientific content to diverse audiences.
• Comfortable learning new roles and 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 understand and communicate with stakeholders from a range of disciplines.
• Ability to develop expertise in new fields through research and networking.
• Excellent knowledge of spoken and written English.
Desirable:
• Prior experience in clinical research, preferably in more than one therapeutic area or indication.
• Can easily communicate with clients and all levels within the organization.
• Prior experience with patient-reported outcome measures (PROs) or Clinical Outcome Assessments (COAs).
Does this sound like something you’d like to explore? Then we’d love to hear from you!
Please apply below. We review and respond to every application, keep an eye on your inbox for our reply.
Please note that Signant does not accept unsolicited resumes from Third Party vendors.


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. Signant Health is proud to be an equal opportunity workplace and is an affirmative action employer. We are 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.