Manager of Hematology and Hospital Clinical Research

Sarah Cannon Research Institute•Nashville, TN

4d•Onsite

About The Position

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. As the Manager of Hematology and Hospital Research Operations you will provide oversight for day-to-day clinical operations of the Hematology/Hospital Research team. Oversee and manage day-to-day activities of the nurses and CRCs Oversee clinical trial-related activities completed/performed by the Research Nurse/CRC to assure completeness, accuracy, compliance, and adherence to federal and state guidelines Participate in trial feasibility, clinical operations review and supporting trial implementation. Lead slot management for monthly enrollment to ensure appropriate clinical trials are prioritized and accrued Assess the organizational processes associated with trial execution and identifies ways to improve and streamline internal procedures. Manage performance and professional development of the research nurses and CRCs including hiring, onboarding, and training. Problem-solve clinical situations along with research nurses as they arise. Assess the organizational processes associated with trial execution and identifies ways to improve and streamline internal procedures. Promote communication and accountability between colleagues and physicians as well as hospital and clinic leadership. Provide coverage and assistance with ongoing research as needed. Keep executive team abreast of issues, progress, and risks related to trial operations and the overall clinic and will meet frequently with all investigators. First point of escalation for MDs, Physicians, Sponsors, etc. Assist in developing and executing internal and external strategies in partnership with internal and external stakeholders. Represent the company vision at the clinics Responsible for individual site goals, financial performance, quality assurance, oversight and contracted patient enrollment. Assist senior leaders to ensure continuing education and training to investigators and coordinators. Ensure colleagues are compliant with applicable protocols throughout the screening, enrolling and following of study subjects.

Requirements

Working knowledge of medical terminology
Clinical knowledge and nursing skills as required by job responsibilities
Registered Nurse with active license in Tennessee
At least three years of experience in clinical research
Supervisory experience

Nice To Haves

OCN certification is preferred
CCRC, ACRP and SOCRA preferred

Responsibilities

Oversee and manage day-to-day activities of the nurses and CRCs
Oversee clinical trial-related activities completed/performed by the Research Nurse/CRC to assure completeness, accuracy, compliance, and adherence to federal and state guidelines
Participate in trial feasibility, clinical operations review and supporting trial implementation.
Lead slot management for monthly enrollment to ensure appropriate clinical trials are prioritized and accrued
Assess the organizational processes associated with trial execution and identifies ways to improve and streamline internal procedures.
Manage performance and professional development of the research nurses and CRCs including hiring, onboarding, and training.
Problem-solve clinical situations along with research nurses as they arise.
Promote communication and accountability between colleagues and physicians as well as hospital and clinic leadership.
Provide coverage and assistance with ongoing research as needed.
Keep executive team abreast of issues, progress, and risks related to trial operations and the overall clinic and will meet frequently with all investigators.
First point of escalation for MDs, Physicians, Sponsors, etc.
Assist in developing and executing internal and external strategies in partnership with internal and external stakeholders.
Represent the company vision at the clinics
Responsible for individual site goals, financial performance, quality assurance, oversight and contracted patient enrollment.
Assist senior leaders to ensure continuing education and training to investigators and coordinators.
Ensure colleagues are compliant with applicable protocols throughout the screening, enrolling and following of study subjects.