About the position
Current UC employees must apply internally via
SuccessFactors
Next Lives at the University of
Cincinnati
Founded in 1819, the University of Cincinnati ranks among
the nation’s best urban public research universities. Home to more
than 53,600 students, 12,000 faculty and staff, and over 360,000
living alumni, UC, a Carnegie 1 institution, combines research
prowess with a physical setting The New York Times has called “the
most ambitious campus design program in the country." UC's momentum
has never been stronger as the anchor of the Cincinnati Innovation
District, the oldest cooperative education (co-op) program in the
country with students earning $94 million annually through paid
experiences, an academic health system, and as a member of the Big
12 Conference. The university contributes $10.6 billion in economic
impact to the city and $22.7 billion to the state of Ohio. At UC,
next is all of us. Learn more at uc.edu.
UC is a mission-driven organization where we are committed
to student success and positively transforming the community
through scholarship and service. We thrive on innovation, making an
impact, and fostering an environment where staff and faculty are
key contributors to UC’s success.
Job Overview
As one of the oldest medical schools in the country, the
University of Cincinnati College of Medicine (COM) has a reputation
for training best-in-class health care professionals and developing
cutting-edge procedures and research that improves the health and
clinical care of patients. In partnership with the UC Health
academic healthcare system and Cincinnati Children’s Hospital
Medical Center, College of Medicine’s faculty are transforming the
world of medicine every day.
A full-time Clinical Research Manager position is
available in the UC Cancer Center at the University of Cincinnati
College of Medicine. The University of Cincinnati Cancer Center
(UCCC) Clinical Trials Office (CTO) is an institutional resource
within the University of Cincinnati College of Medicine and UC
Health that provides administrative, operational, and data
management support for cancer clinical trials conducted by UC
Investigators. The Clinical Research Manager (Education) leads the
development, implementation, and evaluation of education and
training programs for CTO personnel and other professionals engaged
in human-subjects research, including clinical research
coordinators, data personnel, regulatory and quality assurance
staff, investigators, and other clinical staff. The position
applies expert knowledge of clinical research practices and
regulations to promote compliant, consistent, and safe
implementation of Phase I-IV oncology clinical trials across
disease sites. The incumbent will work under the direct supervision
of the UCCC CTO Quality Assurance Manager and works collaboratively
with the UCCC CTO Administrative Director and CTO Medical Director,
Clinical Research Managers, QA team members, and other departmental
and institutional stakeholders.
Essential Functions
- Develop, implement, and evaluate oncology research orientation
& training programs for CTO personnel promoting the use of
hands-on simulations, team-based multidisciplinary practices and
utilizing multiple adult-learner focused strategies.
- Independently design, coordinate, implement and evaluate a
variety of formal continuing education programs for research
personnel based on identified learning needs, emerging trends in
research, regulatory changes, quality findings, and new or revised
processes and practices, etc.
- Design, implement, maintain, and evaluate educational platforms
and metric-capture systems including Canvas and REDCap to meet CTO
educational and training needs and initiatives.
- Prepare and present reports on educational initiatives, learner
outcomes, and training metrics for internal and external
stakeholders.
- Coordinate the CTO Process Improvement Committee (PIC) ensuring
all proposed changes or new policies, workflows, SOPs or other
procedural documents are reviewed per the PIC Charter.
- Develop, implement and maintain repositories for all internal
CTO policies, workflows and SOPs, including processes for routine
review, accuracy verification, staff training, acknowledgment, and
renewal.
- Provide in-person instruction in clinical settings on research
best practices and departmental expectations for research staff and
clinicians.
- Provide training and guidance to CTO Preceptors and evaluate
effectiveness of Preceptors (adjusting assignments as needed) in
collaboration with Clinical Research Managers.
- Mentor and assist new employees in assimilating successfully
into the CTO, ensuring timely communication of any issues to the
employee’s direct supervisor and providing required/directed
continuing education as applicable in collaboration with the direct
supervisor.
- Provide research role-specific training to researcher
physicians and APPs external to the department as needed. Includes
coordination of Fellows and/or Resident research rotations within
the CTO.
- Coordinate obtaining continuing education credits for
continuing education offerings through professional societies
(e.g., SOCRA, ACRP, RAPS, etc.)
- Oversee adherence and provide guidance related to all relevant
internal/external SOPs, policies, and workflows, Good Clinical
Practice, and FDA regulations.
- Holds leadership roles in Departmental or Institutional
committees relating to clinical research compliance and/or
education.
- Provides daily management/supervision to the clinical research
education team.
- Assists CTO leadership and QA Manager in developing strategic
planning goals and initiatives for clinical research education,
quality, compliance, and workforce development.
- Other job duties as needed to support the education and
training initiatives of the CTO.
Required Education
- Bachelor’s Degree
- Nine (9) years of relevant work experience and/or other
specialized training can be used in lieu of education
requirement.
Required Trainings/Certifications
- N/A
Required Experience
- Five (5) years related experience.
Additional Qualifications Considered
- Experience in an academic or clinical setting in the area
of clinical specialization.
- SoCRA or ACRP certification.
- Experience in oncology clinical research.
- Strong written, verbal, and interpersonal communication
skills with ability to maintain effective communication with
internal employees, managers, investigators, and stakeholders as
needed.
- Strong analysis and independent problem-solving
skills.
- Ability to integrate and apply feedback in a professional
manner.
- Ability to prioritize tasks and drive results with a high
emphasis on quality.
- Ability to work independently and as part of a
team.
- Previous supervisory or management
experience.
Physical Requirements/Work Environment
- Sitting - Continuously
Compensation and Benefits
UC offers an exceptional benefits package designed to
support your well-being, financial security, and work-life
balance. (UC
Benefits) Eligibility may vary by position and FTE
status. Highlights include:
Comprehensive Tuition
Remission
UC provides tuition remission for you and your eligible
dependents, covering tuition costs for nearly all undergraduate and
graduate programs offered by the university.
Robust Retirement Plans
As a UC employee, you won’t contribute to Social Security
(except Medicare). Instead, you’ll choose between state pension
plans (OPERS, STRS) or an Alternative Retirement Plan (ARP), with
UC contributing 14–18% of your salary based on position.
Real Work-Life Balance
UC prioritizes work-life balance with a generous time-off
policy, including:
Vacation and sick time
11 paid holidays and additional end-of-year paid time off
(Winter Season Days)
6 weeks of paid parental leave for new parents
Additional Benefits Include:
- Competitive salary based on experience
- Comprehensive health coverage (medical, dental, vision,
prescription)
- Flexible spending accounts & wellness
programs
- Professional development & mentorship
opportunities
To learn more about why UC is a great place to work,
please visit our Careers
Page.
UC is an E-Verify employer. If hired into this position,
you will be required to provide satisfactory proof of employment
eligibility by providing acceptable, original forms of
identification for employment verification via the Federal I-9
employment verification process. Click here
for a list of acceptable documents.
Important: To apply you must
create a profile and submit a complete job application through the
UC applicant portal. We
are unable to consider “easy apply” applications submitted via
other websites. For questions about the UC recruiting process or to
request accommodations with the application, please contact UC HR
at jobs@uc.edu.
Equal Opportunity Employer. Building a workplace
where all qualified applicants will receive consideration for
employment, including Individuals with Disabilities and Protected
Veterans.
REQ: 104455
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