Clinical Research Coor-Multidisciplinary

Job Description:

Clinical Research Coor-Multidisciplinary

Description

Clinical Research Coor-Multidisciplinary
41158BR
41158BR

Position Description
Coordinates daily operations of clinical research studies in assigned department(s). This includes but is not limited to overall clinic conduct, marketing, and data management of all clinical research activities in assigned department(s). Carries out supervisory responsibilities in accordance with policies and applicable laws. Responsibilities may include training new employees; assisting with planning, assigning, and directing work; addressing complaints and resolving problems. The employee is frequently exposed to fumes or airborne particles. The employee is occasionally exposed to toxic or caustic chemicals and dangerous bodily fluids. The noise level in the work environment is usually moderate. Approximately 5-15% travel (often long-distance) is required.

Major/Essential Functions

• Develop and maintain relationships with faculty members interested in or currently conducting clinical research.
• Develop and maintain relationships with assigned pharmaceutical, medical device, and other medical manufacturers considering clinical trials.
• Actively market the Clinical Research Institute.
• Facilitate IRB application and submission via iRIS system.
• Facilitate ongoing and timely communication with the IRB via iRIS system.
• Recruit and enroll human subject while protecting subjects and subjects' rights.
• Maintain Study files/documents on all assigned studies.
• Facilitates data quality and integrity.
• Assist with development and management of research study budget.
• Assist faculty/staff with development of research protocols.
• Assist with clinical research education and training of volunteers, students, new employees.
• Attend affiliated clinical research meetings and professional meetings where research and compliance training may occur.
• Obtain SoCRA (CCRP) or ACRP (CCRC) certification when eligible.
• Maintain CPR certification.
• Maintain IATA training/certification.
• Maintain required institutional training to be able to participate in Clinical Research activities (i.e. CITI and HIPAA research training).
• Maintain Texas nursing or other healthcare provider licensure.
• Facilitates data quality and integrity.
• Participate in the Clinical Research call schedule rotation as needed.
• Obtain and maintain appropriate credentialing approval from University Medical Center Medical Staff office.

Required Qualifications
Healthcare-related training with current licensure/certification in their field .OR Bachelor's degree from an accredited university with a major in the area of research being conducted.
Certification:
Certified Clinical Research Professional as defined by The Society of Clinical Research Associates or Certified Clinical Research Coordinator as defined by the Association of Clinical Research Professionals.
OR
Ability to obtain certification as a Clinical Research Professional/Coordinator within two years from date of hire or upon eligibility.

To apply, please visit: https://sjobs.brassring.com/TGnewUI/Search/home/HomeWithPreLoad?partnerid=25898&siteid=5283&PageType=JobDetails&jobid=890621

All qualified applicants will be considered for employment without regard to sex, race, color, national origin, religion, age, disability, protected veteran status, or genetic information.

The Jeanne Clery Disclosure of Campus Security Policy and Campus Crime Statistics Act is a federal statute requiring colleges and universities participating in federal financial aid programs to maintain and disclose campus crime statistics and security information. By October 1 of each year, institutions must publish and distribute their Annual Campus Security Policy & Crime Statistics Report (ASR) to current and prospective students and employees. You can locate this report through our website at: https://www.ttuhsc.edu/emergency/clery-report.aspx.








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