Clinical Trial Associate

Job Description
The Role:
We are seeking a Clinical Trial Associate (CTA) to assist and provide support to the members of the clinical operations project team in order to facilitate the management of the clinical trial processes, including planning and execution of clinical trials. The CTA assists in supporting the conduct of trials and may be responsible for managing specific study and operational tasks.
What You’ll Do:
Maintain study trackers and tools as directed by the CPM
Support site start-up activities
Assist study team with preparation for audits/inspections
Assist in creating, editing, and distributing informed consent templates, manuals and other study documents
Track 1572s and liase with Regulatory for IND submission as well as other essential documents as appropriate
Perform Trial Master File (TMF) QC
Perform quality control review of documents
Assist with sample management
May provide study-specific training and mentoring to CRAs and site staff
May develop and maintain study documents
May participate in review of study core documents (protocol, IB, CSR)
Demonstrates excitement around the Vison and Mission of Deciphera and the department
Other duties as assigned