
Manager, Research
Louisville, KYFull-timeSeen 1w agoSeen in employer's feed 2 days ago
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At a glance
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Job overview
The University of Louisville’s Department of Neurology seeks a Manager of Research to lead clinical and translational research initiatives, primarily focused on stroke and cerebrovascular disease. The role oversees clinical trials, studies, registries, collaborations, and funded research, coordinating teams and managing implementation, budgets, resources, timelines, quality, and regulatory compliance. The manager also supports investigators and helps strengthen the department’s research infrastructure.
Skills & qualifications
Skills
Qualifications
Full job description
Compensation
$
Hours Per Week
37.5
Number Of Positions
1
Job Description
Minimum Requirements:
Bachelor's degree in a related field and four (4) years of relevant experience or an equivalent combination of education and experience. Grade 7 (Salaried)
Position Description:
The Department of Neurology at the University of Louisville is seeking an experienced, highly organized, and collaborative Manager of Research to oversee clinical and translational research initiatives, with a primary focus on stroke and cerebrovascular disease.
This position provides operational and project management leadership for clinical trials, investigator-initiated studies, registries, multicenter collaborations, and federally funded research. The Manager will coordinate multidisciplinary teams, oversee project implementation, monitor budgets and resources, and ensure research activities meet established timelines, quality standards, and regulatory requirements.
Working closely with faculty investigators, clinical teams, research personnel, institutional offices, sponsors, and external collaborators, the Manager will strengthen the department's research infrastructure, support faculty investigators, and facilitate the growth of its clinical and translational research portfolio.
Primary Responsibilities
Provide project management and operational oversight for assigned clinical and translational research initiatives, including clinical trials, investigator-initiated studies, registries, and federally funded projects.
Develop and maintain project plans, timelines, milestones, enrollment goals, and performance tracking systems to ensure timely completion of research activities.
Coordinate regulatory submissions, study documentation, monitoring visits, and quality assurance activities to ensure compliance with institutional policies, sponsor requirements, and applicable regulations.
Oversee patient recruitment, enrollment, study visits, and follow-up activities in collaboration with clinical teams and research personnel.
Monitor research data collection, documentation, quality, and reporting; prepare project updates and progress reports for investigators, sponsors, and departmental leadership.
Provide operational leadership and oversight to assigned research personnel, including coordinating workloads, training, staffing needs, and project responsibilities.
Coordinate research budgets, resources, contracts, and study start-up activities in collaboration with faculty investigators and institutional offices.
Support the development and implementation of new research initiatives, standardized workflows, and opportunities to expand research collaborations and improve operational efficiency.
Preferred Qualifications
Master's degree in clinical research, public health, neuroscience, healthcare administration, project management, or a related field.
Four or more years of experience managing clinical research projects, research operations, or complex healthcare initiatives.
Experience coordinating clinical trials, including study start-up, patient recruitment, regulatory submissions, monitoring, and study closeout.
Experience with IRB processes, Good Clinical Practice, human subjects research protections, and regulatory documentation.
Experience managing multiple projects, timelines, deliverables, and competing priorities.
Experience supervising, training, or coordinating research personnel and multidisciplinary teams.
Experience with research budgets, resource planning, sponsor communications, and institutional research administration.
Proficiency with REDCap, electronic medical records, clinical research databases, and project management tools.
Experience in academic medicine, neurology, stroke, cerebrovascular disease, or another clinical specialty.
Experience supporting investigator-initiated, multicenter, industry-sponsored, or federally funded research.
Clinical Research Coordinator (CCRC), Certified Clinical Research Professional (CCRP), Project Management Professional (PMP), or other relevant certification preferred.
Compensation will be commensurate to candidate experience.
Equal Employment Opportunity
The University of Louisville is an Equal Employment Opportunity employer. The University strives to provide equal employment opportunity on the basis of merit and without unlawful discrimination on the basis of race, sex, age, color, national origin, ethnicity, creed, religion, disability, genetic information, sexual orientation, gender, gender identity or expression, veteran status, marital status, or pregnancy. In accordance with the Rehabilitation Act of 1973 and the Vietnam Era Veteran Readjustment Act of 1974, the University prohibits job discrimination of individuals with disabilities, Vietnam era veterans, qualified special disabled veterans, recently separated veterans, and other protected veterans. The University acknowledges its obligations to ensure affirmative steps are taken to ensure equal employment opportunities for all employees and applicants for employment. It is the policy of the University that no employee or applicant for employment be subject to unlawful discrimination in terms of recruitment, hiring, promotion, contract, contract renewal, tenure, compensation, benefits, and/or working conditions. No employee or applicant for employment is required to endorse or condemn a specific ideology, political viewpoint, or social viewpoint to be eligible for hiring, contract renewal, tenure, or promotion.
Consistent with applicable law, demographic information is collected for aggregate reporting requirements. Demographic information provided through this application is not available to hiring managers/committees and is not considered in hiring or employment decisions.
Assistance and Accommodations
Computers are available for application submission at the Human Resources Department located at 2315 South First Street Walk, Room 02C - Louisville, Kentucky 40292.
If you require assistance or accommodation with our online application process, please contact us by email at [email protected] or by phone 502-852-6258.
Equal Employment Opportunity (EEO) Employer
Yes
Americans with Disabilities Act (ADA) compliant
Yes
Background Check Required
Yes
Place of Work
On-site
Requisition ID
R109624
How this job compares
Set against the 1,452 open Clinical Research jobs on Olive Jobs, counted November 13, 2026.
- Pay
- This postingNot listed
- US median$129–198K/yr737 salary ranges
- US median$26–36/hr192 hourly ranges
- Openings
- Olive Jobs lists 20 open Clinical Research jobs in Kentucky and 1,452 across the US. 12% of them nationwide are listed as remote or flexible.
- Hiring the most in Kentucky
- Syneos Health/ inVentiv Health Commercial LLC8 open
- Baptist Health4 open
- IQVIA2 open
- Experience
- This posting asks for at least 4 years of experience; Clinical Research postings that state a minimum ask for 3 years at the median (1,098 postings).
- Education
- 573 of the 1,452 open Clinical Research jobs (39%) ask for a bachelor's degree or higher.
Counted across the open, public US postings on Olive Jobs on November 13, 2026. Figures based on too few postings are left out.
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