Tnonc
Research Study Activation Specialist
TNO - GHCR Admin | Nashville, TN
Sponsorship not specifiedDetected 16 days ago
GCPClinical TrialsClinical ResearchFDA RegulatoryResearchCommunication
About the role
- Tennessee Oncology is committed to advancing both the science of detection and targeted treatments, and to making these advances available to every patient.
- We believe caring for cancer patients is a privilege.
- Job Description: The Clinical Research Study Activation Specialist plays a crucial role in initiating and managing the startup process for clinical research studies.
Requirements
- Physical Activity Required
Nice to have
- Schedule s, coordinate s, and/or participate s in pre-study and site initiation visits
- Facilitate s communications between the CRO/sponsor during study activation
- Ensure s activation activities comply with GCP, institutional policies, SOPs, and applicable regulatory requirements
- Ensure s required study documents are collected, reviewed, and approved prior to site initiation
- Coordinate s with regulatory, budget/contracting, pharmacy, lab, tissue, data, and clinical operations teams to ensure activation requirements are met
- Facilitate s activation meetings and ensure s clear communication of expectations, responsibilities, and timelines
- Serve s as the primary point of contact for sponsors and CROs for study start-up related activities
- Track s and report s activation metrics (e.g., time to activation, bottlenecks, workload distribution )
Company info
- We are looking for talented and highly-motivated individuals who demonstrate a natural desire to support the meaningful work of community oncologists and the patients we serve.
Visa & Work Authorization
- The specialist will work closely with the CRO/sponsor and appropriate internal staff to ensure st udy activation performance metrics are achieved
This listing is sourced directly from Tnonc's careers page and normalized into a canonical job model.