Clinical Scientist - Digital Health Sciences at Signant Health

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. You will review clinical study protocols from prospective and current customers to identify the scientific and technological requirements of the clinical trial. You 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. You'll be involved in preparing and attending pre-sales, capabilities, and bid defense presentations, and present scientific content. Additionally, the you'll support the development of eCOA solutions, advising client and internal 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:

• Support the commercial team by analysing 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 client and internal study teams ensuring the solution design meets study objectives
• Understand product capabilities, functionalities, and suitability of solutions across different therapeutic indications
• Maintain comprehensive 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

Your influence:

• Considers all products and services in the context of providing the clinical trial study participant with an optimal clinical trial participation experience; provides feedback based on practice for areas of potential research; participates in patient centric research efforts.
• Maintains Signant Health's high regard for scientific expertise and industry leadership.

You’ll need to bring:

• Advanced degree (MSc or PhD) in biological science or related to clinical research
• some work experience in clinical trial technology or related industry
• U nderstanding of clinical research and the drug development cycle
• Familiar with the bridge between technology and science in digital health technologies for clinical trials
• Strong interpersonal and communication skills; ability to understand and communicate with stakeholders from a range of disciplines including clients
• Proven ability to multitasking, time management and task-oriented performance; able to work in a fast-paced environment
• Ability to develop expertise in new fields through research and networking
• Excellent knowledge of spoken and written English

We’d be thrilled to hear that you also have:

• Advanced degree (MSc or PhD) in Cancer/Oncology or Cardiology/Cardiovascular
• 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)