Clinical Program Associate
RemoteUnited States
Job Summary
Track enrollment, study cohorts, and protocol amendments while creating one-page study summaries and circulating them to sites. Draft disease KOL lists, program-specific materials, and Open to Enrollment emails; distribute Therapeutic Development supported materials to the network. Coordinate interventional actions across teams for at-risk studies, assist with slide deck creation, and manage FDA approval communications. Provide materials in support of a SCRI Research Program with manager oversight, including drafting study summary emails and maintaining actions for team initiatives. This remote US-based role supports Clinical Program Scientists in advancing oncology treatments.
Required Qualifications
- Bachelor's Degree
- 3+ years of relevant experience
- Broad oncology OR clinical research (phase I – IV) knowledge
- Willingness to develop in-depth expertise required to support a SCRI Research Program
- Ability to work in cross-functional, multi-cultural teams
- Good verbal and written communication skills
- Good prioritization skills
- Strong ability to function in a dynamic environment and adapt to changing needs of program
- Practices and adheres to the 'Code of Conduct' philosophy and 'Mission and Value Statement'
- Will be routinely assigned training requirements
- Expected to complete any training assignments by the due date
- This is a remote position based in the United States
- Relocation and visa sponsorship are not available
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.