CLINICAL RESEARCH COORDINATOR I

Updated: 2 months ago
Location: Rio Grande City, TEXAS
Deadline: ;

Posting Details
Position Information


Posting Number SRGV7356
Working Title CLINICAL RESEARCH COORDINATOR I
Number of Vacancies 1
Location Harlingen, Texas
Department School of Medicine / Neuro & Behavioral Health ISU
FTE 1.0
FLSA Non-Exempt
Scope of Job
To provide general/entry-level administrative and technical assistance to a research team in all aspects of clinical research operations and ongoing research projects.
Description of Duties
  • Schedules, coordinates, and participates in pre-site visits and site initiation visits, and coordinates study initiation.
  • Maintains data pertaining to research projects and completes source documents/case report forms.
  • Completes data entry into electronic data capture systems (sponsor/study specific).
  • Assists with scheduling to ensure in-window completion of study specific requirements.
  • Develops and maintains working relationship with study monitor.
  • Attends and participates in campus coordinator workshops.
  • Responds to monitor findings.
  • Assists with collection and maintenance of regulatory binder items (CAPs, CLIAs, CVs, etc.).
  • If appropriately trained and tested for competency, obtains Vital Signs and performs phlebotomy.
  • Monitors participant labs and notifies Principal Investigator (PI) of laboratory findings.
  • Assists in processing and shipping lab specimens efficiently, cost effectively and accurately.
  • Develops working relationships with all relevant clinical stakeholders.
  • Attends and presents relevant updates at weekly research team meetings.
  • Maintains supply inventory and equipment; maintains regulatory standards.
  • Performs other duties as assigned.
Supervision Received
General supervision from assigned supervisor.
Supervision Given
None.
Required Education
High School Diploma or equivalent.
Preferred Education
Associate degree from an accredited university or degree in Neuroscience,  Psychology, Biology.
Licenses/Certifications
Preferred: Certified Clinical Research Professional (CCRP) through The Society of Clinical Research Associates.
Required Experience
  • One (1) year of experience in clinical research working with human subjects research, or
  • Two (2) years of work experience in a healthcare setting.
Preferred Experience
Experience obtained in healthcare setting/environment. Experience in phlebotomy.  Experience in conducting recruitment, eligibility screening and scheduling of research participants.  Experience in IRB standards, protocols, data collection, statistical analysis and research.  Experience in lab management for clinical research.  Experience in REDCap and Stata.  English and Spanish.
Equipment
Use of standard medical/office/research equipment.
Working Conditions
Needs to be able to successfully perform all required duties. Healthcare/Clinic/Research/ Office environment; some travel and weekend work may be required. Exerting up to 20 pounds of force frequently, and/or a negligible amount of force constantly to move objects. UTRGV is a distributed institution, which requires presence at multiple locations throughout the Rio Grande Valley.
Other
Excellent communication and written skills, attention to detail and willingness to learn. Ability to organize a variety of data and coordinate multiple concurrent projects.
Physical Capabilities
N/A
Employment Category Full-Time
Minimum Salary Commensurate with Experience
Posted Salary Commensurate with Experience
Position Available Date 02/19/2024
Grant Funded Position Yes
If Yes, Provide Grant Expiration Date 06/30/2026

Posting Detail Information


EEO Statement
It is the policy of The University of Texas Rio Grande Valley to promote and ensure equal employment opportunities for all individuals without regard to race, color, national origin, sex, age, religion, disability, sexual orientation, gender identity or expression, genetic information or protected veteran status. In accordance with the requirements of Title VII of the Civil Rights Act of 1964, the Title IX of the Education Amendments of 1972, Section 504 of the Rehabilitation Act of 1973, and the Americans with Disabilities Act of 1990, as amended, our University is committed to comply with all government requirements and ensures non-discrimination in its education programs and activities, including employment. We encourage women, minorities and differently abled persons to apply for employment positions of interest.
Special Instructions to Applicants
Dear Applicant,
Human Resources will not be held responsible for redacting any confidential information from the documents you attach with your application. The confidential information includes the following:
Date of Birth
Social Security Number
Gender
Ethnicity/Race
Please make sure that you omit this information prior to submission. We are advising that Human Resources will be forwarding your application to the department as per your submission.
If you have any questions, please do not hesitate to contact us at (956)665-8880 and/or [email protected].
Additional Information
UTRGV is a distributed location institution and working location is subject to change based on need.
All UTRGV employees are required to have a criminal background check (CBC). Incomplete applications will not be considered.
Substitutions to the above requirements must have prior approval from the VP of HR & Talent Development .
Quick Link https://careers.utrgv.edu/postings/41837