Research Associate Clinical I



The MCC-Clinical Research Organization seeks to hire a Research Associate Clinical I.

The primary responsibilities for this position include: obtain, abstract and collate data, reports, etc. related to studies. Maintain and submit all reports, forms and updated records to groups required by study. Assist in designing a system for organizing, planning and controlling workflow related to the conduct of clinical studies and protocols.

Coordinate flow of patient through clinical study or protocol, monitoring all events related to patient and communicating any pertinent information to PO and appropriate health professionals.

Learn basics of Good Clinical Practice (GCP) and standard operating procedures (SOP); monitor safety and general well-being of all patients by exercising independent clinical judgment regarding patient care issues and protocol adherence.

Assist investigators with identification and recruitment of patients; ensure that pre-study and eligibility requirements of the protocol have been met for patients, maintain cooperative and professional relationships with all Clinical Research participants; collaborate and consult with other health professionals in planning care for study participation and to ensure protocol compliance; and other duties as assigned.




Job Title
Research Associate Clinical I

Requisition Number
RE12534

Working Title
CRA I Clinical

Department Name
7H024:MCC - CLINICAL RESEARCH ORG

Work Location
Lexington, KY

Grade Level
41

Salary Range
$14.77-23.63/hour

Type of Position
Staff

Position Time Status
Full-Time

Required Education

BS



Click here for more information about equivalencies:
http://www.uky.edu/hr/employment/working-uk/equivalencies

Required Related Experience

1 yr



Required License/ Registration/Certification

None



Physical Requirements

Requires handling of light-weight objects up to 10 pounds, sitting for long periods of time, some standing or walking.



Shift

Monday-Friday 8:00am-4:30pm (40 hrs/wk)



Skills/Knowledge/Abilities

MS windows, Outlook, Excel, and Word.
Experience in research, administrative experience, data management.



Does this position have supervisory responsibilities?
No

Preferred Education/Experience

Bachelor's degree plus one or more years related experience and SoCRA or ACRP certification preferred.



Deadline to Apply
01/28/2018

University Community of Inclusion

The University of Kentucky is committed to a diverse and inclusive workforce by ensuring all our students, faculty, and staff work in an environment of openness and acceptance. We strive to foster a community where people of all backgrounds, identities, and perspectives can feel secure and welcome. We also value the well-being of each of our employees and are dedicated to creating a healthy place to work, learn and live. In the interest of maintaining a safe and healthy environment for our students, employees, patients and visitors the University of Kentucky is a Tobacco & Drug Free campus.

As an Equal Opportunity Employer, we strongly encourage veterans, individuals with disabilities, women, and all minorities to consider our employment opportunities.

Any candidate offered a position may be required to pass pre-employment screenings as mandated by University of Kentucky Human Resources. These screenings may include a national background check and/or drug screen.



Posting Specific Questions

Required fields are indicated with an asterisk (*).

  1. * University of Kentucky HealthCare recognizes a set of values that guide us in our daily interactions. By applying for a position within UK Healthcare, you are indicating your commitment and expressing your agreement to our five values. These values are diversity, innovation, respect, compassion, and teamwork. Please choose one of the UK Healthcare values and give a specific example when you exhibited this quality in your professional experience.

    (Open Ended Question)

  2. * Please select the answer that best describes your years of paid, full-time experience in clinical research.
    • none
    • more than 0, up through 1 year
    • more than 1 year, up through 3 years
    • more than 3 years, up through 5 years
    • more than 5 years
  3. * Please choose the answer that best describes your amount of paid, full-time experience working with IRBs, protocol submissions, and patient consents.
    • None
    • More than 0, up through 1 year
    • More than 1 year, up through 2 years
    • More than 2 years, up through 3 years
    • More than 3 years
  4. * Please select which of the following best represents your educational training.
    • Less than high school diploma or GED
    • High school diploma or GED
    • Associate's degree
    • Bachelor's degree
    • Master's degree
    • PhD
    • Other
  5. * Please select the response that best represents your amount of paid, full-time employment experience working with clinical research studies and/or administering or monitoring research protocols.
    • None
    • More than 0, up through 1 year
    • More than 1 year, up through 2 years
    • More than 2 years, up through 3 years
    • More than 3 years
  6. * Please describe your experience working with clinical research - data management, study coordination, patient care, patient recruitment and/or enrollment.

    (Open Ended Question)

  7. * Where did you first see this position advertised other than on UK's online employment system?
    • InsideHigherEd.com
    • HigherEdJobs.com
    • Diverseeducation.com (Diverse Issues in Higher Education)
    • HERCjobs.org (Higher Education Recruitment Consortium)
    • InsightIntoDiversity.com
    • Latinosinhighered.com
    • HospitalCareers.com
    • Indeed.com
    • LinkedIn.com
    • Institute for Diversity in Health Management
    • A Colleague, Friend and/or Family Member
    • None of the Above


Applicant Documents

Required Documents
  1. Resume
Optional Documents
  1. Cover Letter

PI101556039