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(This is a remote role located in Mexico)*****Want to do the Best Work of Your Life?
**Working at Signant Health puts you at the very heart of the world's most exciting sector - a high-growth, dynamic company in an extraordinary industry.
We're radically changing the clinical trial landscape, driving change through the technology and innovations we create and the services we deliver to our customers.
**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 presenting scientific content.
Additionally, you'll support the development of eCOA solutions, advising client and internal teams and ensuring clinical trials meet their objectives.
You will develop expertise in COA/eCOA across different indications and an understanding of industry trends and advances.
*****As part of our team, your main responsibilities will be**:- Support the commercial team by analyzing study protocols and other relevant study documents and documenting study requirements.- Assist in developing 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 a 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 participation experience; provides feedback basedon practice for potential research areas; 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 Ph.D.) in biological science or related to clinical research.- One to three years of work experience in clinical trial technology or related industry.- Understanding of clinical research and the drug development cycle.- Familiar with the bridge between technology and science in digital health technologies for clinical trials