Clinical Research Associate

at  Amwell

COMPANY DESCRIPTION

Amwell digitally empowers payers, providers and innovators, enabling an ecosystem of care that spans across in-person, virtual and automated care.
Amwell provides a leading hybrid care enablement platform in the United States and globally, connecting and enabling providers, payers, patients, and innovators to deliver greater access to more affordable, higher quality care.
Amwell believes that hybrid care delivery will transform healthcare. The company offers a single, comprehensive platform to support all digital health needs from urgent to acute and post-acute care, as well as chronic care management and healthy living.
With nearly two decades of experience, Amwell powers the hybrid care of more than 55 health plans, which collectively represent more than 90 million covered lives, and many of the nation’s largest health systems, representing over 2,000 hospitals, have access to Amwell solutions.
For more information, please visit Amwell.com.

• To work under the direction of the Head of Research or a person designated by him.
• To provide assistance in conducting research activities, including planning, organizing, conducting, analyzing data and communicating research findings within the overall scope of a research project.
• To coordinate and perform a variety of independent and team activities involved in the design, preparation, implementation, analysis, and documentation of research.
• To lead project-related tasks including collecting and managing data (coordinating the development of forms, and questionnaires, conducting qualitative interviews), writing up research protocols, and carrying out data analysis with support from colleagues.
• To present information on research progress and outcomes to others responsible for the research project and those outside of the research team.
• To provide guidance as required to any support staff and/or research students assisting with the research project.
• To contribute to the preparation of manuscripts for publication, writing results, and discussions relevant to the literature. Handling the submission for publication process including responding to peer reviews and revising manuscripts
• To develop plans for research projects and to discuss the interpretation of results and the preparation of manuscripts for publication with the Chief Science Officer or person designated by him.
• To liaise with ethics committees regarding the submission of required documentation, patient rights, safety, and well-being of research participants.
• To ensure compliance with SOPs and local security guidelines.
• To perform other related duties incidental to the work described herein as well as occasionally supporting with the development of clinical content for online delivery.