Clinical Program Support Associate

McKesson•Usa, TN

About The Position

It’s More Than a Career, It’s a Mission. Our people are the foundation of our success. By joining our growing team at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will have the opportunity to become part of one of the largest community-based cancer programs to advance oncology treatments and improve outcomes for cancer patients across the globe. We look for mission-driven candidates who have a desire to advance the fight against cancer and make a difference in the lives of patients diagnosed with cancer every day. Our Mission People who live with cancer – those who work to prevent it, fight it, and survive it – are at the heart of every decision we make. Bringing the most innovative medical minds together with the most passionate caregivers in their communities, we are transforming care and personalizing treatment. Through clinical excellence and cutting-edge research, SCRI is redefining cancer care around the world. 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. 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).

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

Responsibilities

General tasks in the support of a SCRI Research Program(s). Tasks can include but may not be limited to:
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.
Drafts Open to Enrollment (OTE) emails
One page summaries
Disease committee content
Drafts and sends FDA approval emails
Assists with slide deck creation
Practices and adheres to the “Code of Conduct” philosophy and “Mission and Value Statement.”
During your employment with SCRI, you will be routinely assigned training requirements. You are expected to complete any training assignments by the due date.