Start Date
Immediate
Expiry Date
29 Oct, 25
Salary
64.95
Posted On
29 Jul, 25
Experience
0 year(s) or above
Remote Job
Yes
Telecommute
Yes
Sponsor Visa
No
Skills
Protocol, Clinical Practices, Communication Skills, Clinical Research, New Hires
Industry
Hospital/Health Care
DEPARTMENT:
85296 Wake Forest University Health Sciences - WF Clinical Trial Methods Center of Excellence
Status:
Full time
JOB SUMMARY
The National Center for Clinical Trials (NCCT) is designed to serve as an innovative platform to revolutionize and catalyze the conduct of clinical trials greatly accelerating the translation of scientific findings into improvements in the prevention, diagnosis, and treatment of disease for our communities and patients. The NCCT will offer core services for patient recruitment and enrollment, trial administration and follow-up, and to gather real world data and evidence. The Clinical Trial Methods Center (CTMC) has been established within the Wake Forest University School of Medicine to provide the necessary tools and expertise that the NCCT will access and apply to deliver many of its core services.
This position will be primarily responsible for assessing and reviewing clinical trial sites across a region to ensure general readiness to conduct clinical trials and readiness to conduct specific clinical trials as they are presented. These responsibilities include evaluating and facilitating the development of site expertise and engagement, space to conduct trials, staff training, technology platforms and access, services available at sites to support trials, performance in conducting trials, etc. This position will also be responsible for working with NCCT and site leadership to develop capacity at sites through personnel and equipment purchases as necessary. In addition, this position will be responsible for assessing site readiness to conduct specific trials as needed. This position will work with business development and study coordination teams to streamline communications between all functional groups and facilitate research.
The role also involves coordinating with site leadership and research staff to address any issues that may arise and providing ongoing support to maintain the highest standards of trial conduct. Effective communication and collaboration with various stakeholders are essential to ensure the successful execution of clinical trials.
This position is a hybrid position that requires frequent travel to sites across a specific region (either 1) Wisconsin and Illinois, or 2) North Carolina, South Carolina and Georgia) for evaluation, assessment and relationship building.
EDUCATION/EXPERIENCE
Master’s degree in a relevant discipline such as Health Administration, Nursing, Business, or Basic Science with three years of relevant management experience; or, an equivalent combination of education and experience. Significant experience in managing clinical trial teams at a service line, therapeutic area or at a site level.
SKILLS/QUALIFICATIONS
Excellent verbal and written communication skills. Ability to work independently to develop processes. Ability to travel to affiliate sites and central offices as needed. Familiar with institutional/governmental regulations and guidelines related to clinical research including the elements of Good Clinical Practices.
III. Strategic Infrastructure Development
IV. Reporting
V. Performs other related duties incidental to the work described herein.
SKILLS/QUALIFICATIONS
Excellent verbal and written communication skills. Ability to work independently to develop processes. Ability to travel to affiliate sites and central offices as needed. Familiar with institutional/governmental regulations and guidelines related to clinical research including the elements of Good Clinical Practices.
I. General Site Readiness Assessment
II. Per-Trial Readiness Assessment
III. Strategic Infrastructure Development
IV. Reporting
V. Performs other related duties incidental to the work described herein.
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