CLINICAL RESEARCH COORDINATOR III
Posting Details
Position Information
Posting Number
SRGV9237
Working Title
CLINICAL RESEARCH COORDINATOR III
Number of Vacancies
1
Location
McAllen, Texas
Department
School of Medicine / MDOISU Oncology
FTE
1.0
FLSA
Exempt
Scope of Job
Manages clinical research projects for Principal Investigators (PI) by coordinating and gathering patient data via methods specified in the study protocol, and to provide complex research administrative duties in support of the study to ensure compliance with regulations.
Description of Duties
- Ensures and maintains accurate source documentation and appropriate forms as per protocol including participant records, drug documentation, and reconciling study drug accountability, monitors documentation for quality and accuracy.
- Identifies and recruits clinical research subjects; monitors enrollment goals and modifies recruitment strategies, as necessary; mentors all clinical research personnel regarding enrollment/recruitment.
- Under the direction of the PI, supervises and assists with the preparation and submission of all Institutional Review Board (IRB) and Regulatory Documents to obtain final approval and may draft various communications with sponsor.
- Conducts reviews of ongoing studies and oversees quality assurance of current protocols; maintains a productive working relationship with the study monitor.
- Provides team coordination, communication, training, and quality control. Develops standard operating procedures, compliance forms, and tracking documents.
- Attends and participates in Investigator meetings.
- Applies knowledge in contributing to Good Clinical Practice (GCP) activities and/or other regulatory activities.
- Plans and reviews goals and requirements of any new protocols and coordinates study initiation.
- Develops and provides education materials and training to patients, family members, and clinical staff to assure patient safety and adherence controls.
- Assesses staffing needs based upon current research activity and implements changes in staffing as needed.
- Coordinates with other clinical research staff to plan and design source documentation for protocol.
- Develops and ensures proper procedures for study specific laboratory collection and storage.
- Precepts new clinical research staff and educates research staff regarding scientific aspects or studies.
- Elicits relevant data from sources outside of the hospital or clinic.
- Monitors participants labs and notifies the PI of laboratory findings.
- Assists PI in budget development/invoicing; may monitor accounts.
- Performs other duties as assigned.
Supervision Received
General supervision from assigned supervisor.
Supervision Given
Direct supervision of assigned staff.
Required Education
Bachelor's degree from an accredited university.
Preferred Education
N/A
Licenses/Certifications
Certified Clinical Research Professional (CCRP) through The Society of Clinical Research Associates (SOCRA) or Association of Clinical Research Professionals (ACRP), or eligible to test.
Required Experience
Two (2) years of job-related clinical research experience in a relevant specialty clinical research area or other closely related clinical experience.
Preferred Experience
Experience obtained in a healthcare setting.
Equipment
Use of standard medical/office/research equipment.
Working Conditions
Needs to be able to successfully perform all required duties. Healthcare/research 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 may require presence at multiple locations throughout the Rio Grande Valley.
As part of their essential duties, employees in these roles are expected to maintain a consistent, in-person presence on campus at their assigned locations. Limited exceptions may apply for positions that are approved as hybrid or fully remote in accordance with UTRGV policies.
Other
Excellent communication skills, attention to detail, and ability to work in a highly matrixed environment with multiple departments and stakeholders. Extensive knowledge of best clinical research practices, techniques, and standards.
Physical Capabilities
N/A
Employment Category
Full-Time
Minimum Salary
Commensurate with Experience
Posted Salary
Commensurate with Experience
Position Available Date
12/07/2026
Grant Funded Position
Yes
If Yes, Provide Grant Expiration Date
05/31/2029
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,
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Date of BirthSocial Security Number
GenderEthnicity/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.
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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 Human Resources.
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