Clinical Research Assistant - Alzheimers Disease Center

Department:

SOM KC The Alzheimers Disease Center (ADC)

CRO Staff

Position Title:

Clinical Research Assistant Alzheimers Disease Center

Job Family Group:

Professional Staff

Job Description Summary:

The University of Kansas Alzheimers Disease Research Center (KU ADRC) is a National Institute of Aging P30designated 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 caregivers. In addition we provide a wide variety of both public education and training opportunities for the workforce of tomorrow.

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 prescreening for eligibility data entry maintenance of regulatory files study visit scheduling and collection data within scope of role.

This is a hybrid position therefore the role will require you to complete job duties both onsite at KUMC and virtually from a secure athome work location as determined by the supervisor.

Job Description:

Job Duties Outlined:

• Recruits and educates potential research participants and evaluate potential eligibility for investigatorinitiated and/or industry sponsored studies. Consults with the study coordinator and /or the principal investigator regarding potential eligibility as appropriate.
• May conduct Informed Consent Interviews with participants and study partners as delegated by the PI based on level of training and ADRC Standard Operating Procedures (SOP) for obtaining consent from cognitively normal and cognitively impaired individuals. Assesses capacity to provide consent and utilizes surrogate consent form when appropriate.
• Obtains medical records when appropriate following all institutional policies
• Collects processes handles and ships biological specimens as outlined in the protocol and following KUMC policy. Maintains KUMC certification in biological specimen handling shipping and phlebotomy as appropriate.
• Assists in collection of study data within scope of role and experience under the supervision of the study coordinator.
• Tracks and documents study related activities in a timely and accurate manner as directed.
• Assists with maintaining adequate study supply inventory for the conduct of study visits.
• Assists with study visit activities including scheduling visits and procedures within protocol specified parameters.
• Assists the study coordinator in entering the collected data into sponsors electronic databases within required timeframes. Responds to database queries in a timely manner and consults with the study coordinator as needed.
• Assists with timely and thorough filing of regulatory documents in Investigator Site Files.
• Other duties as requested by supervisor

Required Qualifications

Education: Associates degree. A combination of education and relevant work experience may substitute for degree on a yearforyear basis.

Preferred Qualifications

Education:/Certification:

• Bachelors Degree. A combination of education and relevant work experience may substitute for degree on a yearforyear basis
• Research certification preferred such as certified clinical research professional (CCRP) through Society of Clinical Research Associates (SoCRA) or as a certified clinical research coordinator(CCRC) or other applicable certification through the Association of Clinical Research Professionals (ACRP).

Work Experience:

• Prior health care and/or clinical research experience.
• Working knowledge of medical terminology common medical conditions and medications.

Skills:

• Computer skills: MS Office Suite.
• Excellent communication skills both orally and written.
• Excellent attention to detail organizational skills and time management.

Required Documents:

• Resume/CV
• Cover Letter

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.

Comprehensive Benefits Package: