Clinical Research Supervisor Alzheimer's Disease Center
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Job Location:
Kansas City, KS - USA
Monthly Salary:
$ 75000 - 115000
Posted on:
2 days ago
Vacancies:
1 Vacancy
Job Summary
Department:
SOM KC The Alzheimers Disease Center (ADC)-----
CRO - StaffPosition Title:
Clinical Research Supervisor - Alzheimers Disease CenterJob Family Group:
Professional StaffJob Description Summary:
The University of Kansas Alzheimers Disease Research Center (KU ADRC) is a National Institute of Aging P30-designated national leader in AD research with the vision to impact the lives of every patient and family dealing with Alzheimers in the region and across the state of Kansas through our research education and clinical care. We are a comprehensive center at the forefront of clinical trials lifestyle intervention trials drug and translational research and basic science research. Our research enables us to also provide leading edge clinical care and support for dementia addition we provide a wide variety of both public education and training opportunities for the workforce of tomorrow.The primary function of the Clinical Research Operations Supervisor is to oversee the clinical research staff in day-to-day research operations. This position serves as a mentor and team leader for the clinical research staff. Supervisor duties include setting goals assessing performance and ensuring all staff are meeting or exceeding expectations regarding the conduct of addition to supervising staff this position is responsible for the coordination of assigned research studies.
Job Description:
Job Duties Outlined
- Provide information to assist in the development of internal grant project proposals and budgets.
- Assess workloads and assists in determination of staffing needs and hiring decisions. Facilitates the orientation and training of staff.
- Supervise clinical research staff. Provide feedback on employee performance through annual employee evaluation and regular meetings throughout the year.
- Provide guidance and mentorship in complying with all Federal sponsor KUMC regulatory and other appropriate policies and approved practices.
- Guide and mentor study staff in completing and maintaining all study data source and regulatory documents necessary in appropriate participant and investigator site files.
- Collaborate with study coordinators and manager to ensure study recruitment needs are met.
- Assist in the preparation and conduct of internal and external research audits and inspections.
- Serve as a clinical research coordinator on assigned studies.
This job description is not designed to cover or contain a comprehensive listing of activities duties or responsibilities that are required of the employee for this job. It is only a summary of the typical functions of the job not an exhaustive list of all possible job responsibilities tasks duties and assignments. Furthermore job duties responsibilities and activities may change at any time with or without notice.
Work Environment
This is a hybrid position; therefore the role will require you to complete job duties both onsite at KUMC and virtually from a secure at-home work location as determined by the supervisor.
Required Qualifications
Certification: Research certification such as:
- Certified clinical research professional (CCRP) through Society of Clinical Research Associates (SoCRA).
- Certified clinical research coordinator (CCRC)
- Other applicable certification through the Association of Clinical Research Professionals (ACRP).
Work Experience:
- Eight (8) years of experience in clinical research or related field. Education may be substituted for experience on a year for year basis.
- Experience with FDA regulations and ICH-GCP guidelines.
- Mentorship experience.
Preferred Qualifications
Education: Bachelors degree.
Work Experience:
- Supervisory experience.
Skills
- Computer skills: MS Office Suite
- Communication
- Interpersonal skills
- Attention to detail
- Organization
- Time management
Comprehensive Benefits Package:
Coverage begins on day one for health dental and vision insurance and includes health expense accounts with generous employer contributions if the employee participates in a qualifying health plan. Employer-paid life insurance long-term disability insurance and various additional voluntary insurance plans are available. Paid time off including vacation and sick begins accruing upon hire plus ten paid holidays. One paid discretionary day is available after six months of employment and paid time off for bereavement jury duty military service and parental leave is available after 12 months of employment. A retirement program with a generous employer contribution and additional voluntary retirement programs (457 or 403b) are available. Type: Regular Compensation Statement: The pay range listed for this position is determined by our compensation program using market data and salary benchmarking. A combination of factors is considered in making compensation decisions including but not limited to education experience and training qualifications relative to the requirements of the position and funding. At the University of Kansas Medical Center a reasonable estimate for the starting pay range will be the minimum to midpoint of the posted range taking into account the combination of factors listed above. Minimum Midpoint MaximumTime Type:
Full timeRate Type:
SalaryPay Range:
$75000.00 - $115000.00
Required Experience:
Manager
Key Skills
- CSS
- Cloud Computing
- Health Education
- Actuary
- Building Electrician
About Company
The University of Kansas Medical Center (KUMC), a campus of the University of Kansas located in Kansas City, Kansas, offers educational programs and clinical training through its schools of Health Professions, Medicine, Nursing, and Graduate Studies.
