Clinical Program Associate

Sarah Cannon Research Institute•Work at Home - Tennessee, USA (WTNA), TN

3d•Remote

About The Position

The Clinical Program Associate role will provide administrative and overall support to a Clinical Program Scientist, and/or Associate Director, and/or Director in the support of a SCRI Research Program(s). Therapeutic Development provides centralized oversight of all projects which encompass a SCRI Research Program. These projects result in the execution of disease-specific and organizational research goals.

Requirements

Bachelor's Degree
3+ years of relevant experience, preferably in oncology or clinical research
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.”
Expected to complete any training assignments by the due date.

Responsibilities

Tracks enrollment and updates relevant documents
Tracks study cohorts
Tracks protocol amendments
Creates and updates one page study summaries; circulates to appropriate sites with oversight
In partnership with Disease Program Team, drafts and maintains list of disease KOLs by region/expertise/etc.
Drafts study summary emails for sites; drafts program-specific material for distribution
Distributes Therapeutic Development supported materials to network
Supervise and forward questions to appropriate stakeholders from shared department mailbox
Ad-hoc projects and related work as required
Tracks and maintains actions for Therapeutic Development team initiatives
Coordinate interventional actions across multiple teams for at risk studies
Supports partner enrollment targets that may be inclusive of diversity targets
Provides materials in support of a SCRI Research Program(s) with manager oversight, as appropriate. Includes but may not be limited to: Drafts Open to Enrollment (OTE) emails, One page summaries, Disease committee content, Drafts and sends FDA approval emails, Assists with slide deck creation