Clinical Research Assessment Specialist

# Careers With Purpose Clinical Research Assessment Specialist page is loaded## Clinical Research Assessment Specialist locations:
ND, Fargotime type:
Full time posted on:
Posted Yesterday job requisition :
R-0246937
** Sanford Health is one of the largest and fastest-growing not-for-profit health systems in the United States. We’re proud to offer many development and advancement opportunities to our nearly 50,000 members of the Sanford Family who are dedicated to the work of health and healing across our broad footprint.
*
* Work Shift:

Day (United States of America)
Scheduled Weekly

Hours:

40

Salary Range: $24.00 - $38.50
** Union Position:
** No
* * Department Details
** Sanford Research is searching for a new team member to help conduct assessments and research studies in the areas of eating disorders and bariatric surgery.
Sanford Research - Division of Biobehavioral Research is a clinical research and education facility that is committed to working closely with our clinical colleagues to collaborate on scientific projects aimed at improving the lives of our patients and their families. Individuals in the role of Clinical Research Assessment Specialist primarily conduct psychological assessments and interviews with participants enrolled in our research studies.

Other duties include assisting scientists with successfully running research protocols and interacting closely with participants. As such, competitive candidates for this position will possess strong interpersonal and communication skills, and be motivated to work within a collaborative team environment.
For more information about Sanford Research - Division of Biobehavioral Research, please visit our website at: (Use the "Apply for this Job" box below).-research
** Summary
* * An advanced research position that requires the coordination of, and psychological assessment on, multiple clinical research studies in the areas of bariatric surgery, obesity and eating disorders.
** Job Description
** Must be able to organize complex components of various research projects and clinical trials, including the coordination of study required testing and procedures. Collaborate with principal investigators to ensure safe and compliant investigational treatment or intervention and follow-up per the established research protocol.

Review inclusion/exclusion criteria and source documents to confirm study eligibility. Prepare case report forms and collects source documents for sponsor or audit review. Abstract data from medical records, clinic, consultation and referral notes for preparation of study forms and flow sheets. Review protocol requirements and collaborate with ancillary departments, to include clinic nursing, infusion nursing, pharmacy, radiology, pathology, nurse navigators, dieticians and laboratory personnel to ensure subject safety and protocol compliance.

Responsible for assessment for a number of study protocols, primarily with patients with eating disorders, obesity or have had/will have bariatric surgery. Responsible for dealings with regulatory boards associated with conducting clinical research, such as the Institutional Review Board (IRB).Must be enthusiastic about learning and participating in the education of patients, physicians, nurses and other personnel in the research process, and be a self-motivated, self-directed and autonomous critical thinker to accomplish the daily tasks of the position in partnership with the principal investigators and other members of the research team.
** Qualifications
* * Master's degree in clinically relevant field, to include clinical or counseling psychology required.

** Sanford is an EEO/AA Employer M/F/Disability/Vet.
**** If you are an individual with a disability and would like to request an accommodation for help with your online application, please call or send an email to talent.*
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