University of Texas Rio Grande Valley logo

CLINICAL RESEARCH COORDINATOR III

University of Texas Rio Grande Valley

McAllen, TXFull-timeSeen todaySeen in employer's feed today

Most applications go out cold — see where you stand first. No sign-up to start.

You apply on the employer's site, with no Olive account needed.

Watch jobs like this.

Don't just apply. Show up ready.

Olive works from this exact posting.

At a glance

Compensation
No compensation found
Location
McAllen, TX
Schedule
Full-time
Work Authorization
Not specified

Olive lists jobs from US employers, including remote roles you can work from the United States.

Requirements

Credentials this posting asks for.

Bachelor's degree

Job overview

The Clinical Research Coordinator III manages clinical research projects for Principal Investigators by coordinating patient data collection according to study protocols and supporting regulatory compliance. The role oversees study documentation, recruitment, regulatory submissions, quality assurance, study initiation, staff coordination and training, laboratory procedures, and budget-related tasks. It directly supervises assigned staff and maintains an in-person presence at assigned campus locations.

Skills & qualifications

RequiredNice to have

Skills

Clinical Research CoordinationClinical Research PracticesCommunicationAttention to DetailMatrixed Collaboration

Qualifications

Bachelor's DegreeCCRP or ACRP Certification or Eligible to Test2 Years Clinical Research ExperienceHealthcare Setting Experience

Full job description

Position Information

Posting NumberSRGV9237

Working TitleCLINICAL RESEARCH COORDINATOR III

Number of Vacancies1

LocationMcAllen, Texas

DepartmentSchool of Medicine / MDOISU Oncology

FTE1.0

FLSAExempt

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 CategoryFull-Time

Minimum SalaryCommensurate with Experience

Posted SalaryCommensurate with Experience

Position Available Date12/07/2026

Grant Funded PositionYes

If Yes, Provide Grant Expiration Date05/31/2029

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,

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 Human Resources.

Quick Linkhttps://careers.utrgv.edu/postings/53060

Posting Supplemental Questions

Required fields are indicated with an asterisk (*).

    • Are you now, or previously, employed by The University of Texas System or any of its institutions?
  • Yes - I currently am employed by the UT System or its institutions

  • Yes - I have previously been employed by the UT System or its institutions

  • No - I have never been employed by the UT System or its institutions

    • Are you a current UTRGV employee?
  • Yes

  • No

    • Please select your highest level of completed education.
  • 6th grade education

  • 10th grade education

  • High School Diploma or GED

  • Associates Degree, Technical, or Trade School Degree/Certification or 60 Hours of College Hours

  • Bachelors Degree from an accredited university

  • Masters Degree from an accredited university

  • Ph. D. or other terminal degree from an accredited university

  • None of the above

    • Please provide the field of study for your education:

(Open Ended Question)

    • Please indicate the number of years of work experience you have directly related to the position in which you are applying for:
  • Less than 1 year

  • 1 year

  • 2 years

  • 3 years

  • 4 years

  • 5 years

  • 6 years

  • 7 years

  • 8 years

  • 9 years

  • 10 years

  • Over 10 years

    • Do you meet the minimum requirements for this position?
  • Yes

  • No

Applicant Documents

Required Documents

  • Resume

  • Unofficial Transcripts

  • Certifications and Licenses

Optional Documents

  • Cover Letter/Letter of Application

  • Reference Letter 1

  • Reference Letter 2

  • Reference Letter 3

  • Training Certificates

  • Other Document

  • List of 3 References

  • Unofficial Transcripts 2

  • Unofficial Transcripts 3

  • Letter of Interest

  • Unofficial Graduate Transcripts

  • Additional Document

How this job compares

Set against the 641 open Clinical Research Coordinator jobs on Olive Jobs, counted November 8, 2026.

Pay
  • This postingNot listed
  • US median$56–74K/yr162 salary ranges
  • US median$24–36/hr201 hourly ranges
Openings
Olive Jobs lists 42 open Clinical Research Coordinator jobs in Texas and 641 across the US. 2% of them nationwide are listed as remote or flexible.
Hiring the most in Texas
Experience
This posting asks for at least 2 years of experience; Clinical Research Coordinator postings that state a minimum ask for 2 years at the median (420 postings).
Education
This posting asks for a bachelor's degree; 191 of the 641 open Clinical Research Coordinator jobs (30%) ask for a bachelor's degree or higher.

Counted across the open, public US postings on Olive Jobs on November 8, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.

Prepare for this role

You've read the whole posting — now see how you match it.