at University of Kansas Medical Center in Kansas City, Kansas, United States
Job Description
Clinical Research Assistant - Alzheimers Disease Research Center
Department:
SOM KC The Alzheimer's Disease Center (ADC)
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CRO - Staff
Position Title:
Clinical Research Assistant - Alzheimer's Disease Research Center
Job Family Group:
Professional Staff
Job Description Summary:
The Clinical Research Assistant assists in entry level clinical research activities. Under general supervision, the Clinical Research Assistant works with multidisciplinary teams including patients/study participants, families, physicians, administrative staff, and sponsor and CRO representatives to assist in coordination of all aspects of clinical research. This encompasses study recruitment, pre-screening for eligibility, data entry, maintenance of regulatory files, study visit scheduling, and collection data within scope of role.
The University of Kansas Alzheimer's 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 Alzheimer's 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 caregivers. In addition, we provide a wide variety of both public education and training opportunities for the workforce of tomorrow.
Job Description:
Job Duties Outlined
- Recruit and educate potential research participants and evaluate potential eligibility for investigator-initiated and/or industry sponsored studies. Consults with the study coordinator and /or the principal investigator regarding potential eligibility as appropriate.
- Conduct Informed Consent Interviews with participants and study partners as delegated by the PI based on level of training and experience. Follow ADRC Standard Operating Procedures (SOP) for obtaining consent from cognitively normal and cognitively impaired individuals. Assess capacity to provide consent and utilizes surrogate consent form when appropriate.
- Obtain medical records when appropriate following all institutional policies.
- Collect, process, handle, and ship biological specimens as outlined in the protocol and following KUMC policy. Maintain KUMC certification in biological specimen handling, shipping, and phlebotomy as appropriate.
- Assist in collection of study data within scope of role and experience under the supervision of the study coordinator.
- Track and document study related activities in a timely and accurate manner as directed.
- Assist with maintaining adequate study supply inventory for the conduct of study visits.
- Assist with study visit activities including scheduling visits and procedures within protocol specified parameters.
- Assist the study coordinator in entering the collected data into sponsors' electronic databases within required timeframes. Respond to database queries in a timely manner and consults with the study coordinator as needed.
- Assist with timely and thorough filing of regulatory documents in Investigator Site Files.
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
Work Experience:
- Two (2) years of relevant work experience. Education may be substituted for experience on a year for year basis.
Preferred Qualifications
Education:
- Bachelor's Degree.
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:
- Health care and/or clinical research experience.
- Experience with medical terminology, common medical conditions, and medications.
Skills
- Computer skills
- Communication
- Attention to detail
- Organization
- Time management
Required Documents
- Resume/CV
- Cover Letter
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. https://www.kumc.edu/human-resources/benefits.html
Employee Type:
Regular
Time Type:
Full time
Rate Type:
Hourly
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.
Pay Range:
$22.66 - $32.85
Minimum
$22.66
Midpoint
$27.75
Maximum
$32.85
Application Instructions:
To learn more and apply online, please visit https://kumc.wd5.myworkdayjobs.com/en-US/kumc-jobs/job/Kansas-City-Metro-Area/Clinical-Research-Assistant---Alzheimer-s-Disease-Research-Center_JR009323 or go to https://careers.kumc.edu/ and search for position number JR009323.
Applications must be submitted directly through the KU Medical Center website to be considered for this position. Any applications submitted via email or this website will NOT be reviewed or considered.
About KU Medical Center:
The University of Kansas Medical Centers mission is to educate exceptional health care professionals through a full range of undergraduate, graduate, professional, postdoctoral and continuing education programs in the schools of Medicine, Nursing and Health Professions. KU Medical Center also advances the health sciences through world-class research programs; provides compassionate and state-of-the-art patient care in an academic medical center environment; and works with communities in every Kansas county to improve the health of Kansans. Learn more at www.kumc.edu.
Benefits:
KUMC offers a range of great benefits that support employees and eligible family members. Our health insurance benefits begin on hire date and KUMC offers other exciting benefits such as paid parental leave, generous employer retirement contributions and other resources to improve health and well-being. For more information, please visit https://www.kumc.edu/human-resources/benefits.html
Equal Employment Opportunity Statement
The University of Kansas Medical Center is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, national origin, ethnicity, ancestry, age, protected veteran or disability status, marital status, parental status, or genetic information. http://policy.ku.edu/IOA/nondiscrimination
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