Clinical Study Coordinator

Job Summary:

Responsible for the organization, implementation and administration of clinical research for the Department of Neurological Sciences. Provides coordination of research activities while planning, organizing and executing related daily clinical research activities (e.g. coordinator would: help evaluate research protocols for feasibility, help organize research team working on research project, assist in subject recruitment, know all details of study protocol and implements study procedures as specified, coordinate subject study visits, enter all required information into Nebraska Medicine EMR, participate in data collection and completion of clinical research documents, including electronic data entry, assist in tracking all study visits, which may include assisting in IRB continuing renewal applications and assisting in the tracking and reconciling of research study budgets). Complies with all regulations regarding studies that involve human research participants.

Additional Info

About Us:

To learn more about the University of Nebraska, visit the sites below.

University of Nebraska Strategic Plan â??Odyssey to Extraordinaryâ? https://nebraska.edu/strategic-plan

Get to know Nebraska https://nebraska.edu/get-to-know-nebraska

University of Nebraska Medical Center Campus https://www.unmc.edu/aboutus/index.html and https://www.unmc.edu/aboutus/facts.html

University of Nebraska Faculty & Staff Benefits https://nebraska.edu/faculty-and-staff

Required Qualifications:

• Bachelor's degree
• 2 years clinical experience and/or research experience in a clinical or laboratory setting. 
• Microsoft Word, Microsoft Suite

 

Will consider six years education and/or related experience combined of which two years must include post high school education.

 

• Ability to be certified to collect, prepare and ship biological specimens.
• Working knowledge of clinical trial design.Skill in interviewing subjects and family members.
• Ability to work independently and under competing deadlines.
• Ability to work effectively with people of varying educational and experiential backgrounds.
• Excellent oral and written communication.
• Strong critical thinking, problem solving, and attentiveness to detail skills.

Preferred Qualifications:

• Bachelor's degree in Health Science field/Social Sciences with concentration in research
• Clinical research experience in an academic institution setting
• Certification/maintenance of certification as a Clinical Research Professional (SOCRA) or Clinical Research Coordinator (ACRP)
• Epic One Chart

Compliance Requirements:

• Physical Exam
• Drug Screen
• Background Check
• Child & Adult Sexual Abuse Registry Request and Check
• Education Crednetials Check