Job Description

Are you ready for the Most Impactful Work of Your Life?Signant Health is a global evidence-generation company. Were 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 worlds most exciting sector - a high-growth, dynamic company in an extraordinary industryWhere do you fit in?The Clinical Scientist in the Digital Health Sciences team will provide scientific consultation to internal and external stakeholders on the use of eCOA and other digital health technologies, including eConsent and sensors and wearables, in clinical trials. The Clinical Scientist will review clinical study protocols from prospective and current customers to identify scientific and technological requirements of the clinical trial and provide advice on solution design and development. The Clinical Scientist will support pre-sales, capabilities, bid defense, requirement gathering, and design meetings. Additionally, the Clinical Scientist will provide scientific input to product development to ensure that new capabilities address the scientific requirements of future implementations, and work on marketing initiatives. The Clinical Scientist will provide consultation services through special client or internal projects and research initiatives.Want to join the Best Team of Your Life?Were looking for people who are excited by the potential to make a difference in the world. You dont need to have a clinical background to thrive at Signant. You need to be decisive, open to celebrating mistakes, able to communicate transparently and inclusively, and someone your team can count on. Most of all you need to be yourself!As part of our team, your main responsibilities will:

• Support the commercial team by analysing study protocols and other relevant study documents, documenting study requirements and presenting scientific content in client meetings.
• Advise technical, operations, and client teams on the development of eCOA solutions to ensuring the solution design meets the clinical trial objectives.
• Provide consultation services in the form of special projects on client-specific scientific requests or external initiatives.
• Maintain comprehensive knowledge of the most recent industry best practices and regulatory requirements for clinical outcome assessments (COA).
• Stay on the leading edge of eCOA and digital health technologies through participation in industry forums and working groups, and through collaboration with clients, Key Opinion Leaders.
• Develop thought leadership materials and relevant scientific and research content to demonstrate the companys scientific expertise internally and externally.
• Present and promote Signant Health in the industry, including active participation in industry forums, conferences, presentations, webinars and publications on selected topics.
• Manage time across multiple concurrent projects.
• Develop training and marketing materials.

DECISION MAKING AND INFLUENCE

• Facilitates and maintains team and company culture of collegiality, respect, and professional support.
• Considers all products and services in the context of providing the clinical trial study participant with an optimal clinical trial participation experience; identifies and drives areas for product and service improvement; provides feedback based on practice for areas of potential research; participates in patient centric research efforts.
• Likewise considers all products and services in the context of the clinical trial research study sites.
• Maintains Signant Health as highly regarded for scientific expertise and industry leadership.

Youll need to bring:Essential:

• Advanced degree (PhD preferable) in biological science or healthcare.
• 1-3 years experience in clinical trial technology or related industry, preferably in 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/wearables.
• Proven ability to multitasking, time management and task-oriented performance; able to work in a fast-paced environment.
• Business driven and business growth savvy.
• Familiar with the bridge between technology and science in digital health technologies for clinical trials.
• Proven ability to be an effective, positive team player who can work across teams and in a matrix environment.
• Ability to develop expertise in new fields through research and networking
• Excellent knowledge of spoken and written English

Desirable:

• Prior experience in commercial pre-award activities, such as capabilities and bid-defense meetings, and/or solution design and requirement gathering
• Experience in the development and use of ePRO or eCOA solutions for clinical trials
• Can easily communicate with clients and all levels within the organization

Does this sound like youd like to explore? Then wed 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 isnt 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.

Signant Health