The Director of Clinical Research Operations will support the AVP of Clinical Research by driving successful implementation of all administration and operations, supporting all aspects and management of revenue generation & research compliance functions. Responsible for the Development and Central Operational Support for Clinical Research Studies. This position directs a team focused on Project Management, Resource Utilization, Financial Feasibility, CTMS Usage, Protocol Compliance, Research Participant Accrual as well as Safety and Data Quality. This position represents the Office of Clinical Research throughout the Institution, developing policies and programs related to the Administration of Clinical Research Programs. Supports the VP with ongoing development of departmental strategic research vision & mission. Collaborates with the Director of Regulatory Affairs, Investigator Support Research Unit, Director of Research Compliance, as well as the Manager Business Operations/Oncore team.
This position will include provision of support to the CTO Associate Vice President, CTO Medical Director, Director of Regulatory Affairs and Protocol Development and the Regulatory Staff, Quality Assurance team, and Business/Oncore team.
Masters Degree : in related field (Required)
5 Years experience as a Clinical Research Professional (Required)
7 Years experience in a management position (Required)
3 Years experience in oncology clinical trials (Required)
RN-LIC - PA Registered Nurse License (Preferred)
ONCC - Oncology Nursing Cert Corp (Preferred)
CCRC - Cert Clin Research Coordinator (Preferred) or CCRP - Cert Clin Research Prof (Preferred)
To apply, please go to https://tuhs.taleo.net/careersection/jobdetail.ftl?job=216734&lang=en