Student Veterans of America Jobs

Welcome to SVA’s jobs portal, your one-stop shop for finding the most up to date source of employment opportunities. We have partnered with the National Labor Exchange to provide you this information. You may be looking for part-time employment to supplement your income while you are in school. You might be looking for an internship to add experience to your resume. And you may be completing your training ready to start a new career. This site has all of those types of jobs.

Here are a few things you should know:
  • This site is mobile friendly. You do not need a log-in or password to access information.
  • Jobs on this site are original and unduplicated and come from three sources: the Federal government, state workforce agency job banks, and corporate career websites. All jobs are vetted to ensure there are no scams, training schemes, or phishing.
  • The site is refreshed daily to remove out-of-date content.
  • The newest jobs are listed first, so use the search features to match your interests. You can look for jobs in a specific geographical location, by title or keyword, or you can use the military crosswalk. You may want to do something different from your military career, but you undoubtedly have skills from that occupation that match to a civilian job.

Job Information

UTMB Health Coord, Clinical Research - IntMed-Cardiovascular Medicine in Galveston, Texas

Coord, Clinical Research - IntMed-Cardiovascular Medicine

Galveston, Texas, United States

Research Academic & Clinical

UTMB Health

Requisition # 2400262

JOB SUMMARY:

The Clinical Research Coordinator obtains human subject data for clinical research activities via methods specified in the study protocol and performs general administrative duties supporting the study.

ESSENTIAL JOB FUNCTIONS:

  • Applies knowledge in contributing to Good Clinical Practice (GCP) activities and/or other regulatory activities.

  • Schedules, coordinates, and participates in the pre-site visit and site initiation visits; coordinates study initiation.

  • Maintains and monitors source documentation and appropriate forms as per protocol for quality and accuracy, including participant records; assists with the quality assurance process.

  • Incorporates directions from other health care disciplines into clinical research protocols when reviewing patient eligibility; assists in eliciting relevant data from sources outside of the hospital.

  • Reconciles study drug accountability; maintains temperature and QC logs per protocol compliance.

  • Develops and maintains productive working relationship with the study monitor; attends and participates in campus coordinator workshops.

  • Identifies and recruits clinical research subjects for participation of studies, collects data, and monitors enrollment goals.

  • Mentors new clinical research coordinators and assistant clinical research coordinators.

  • Assists with grant/protocol preparation and submission to IRB, OCR or OSP under direction of research coordinator under the direction of the PI and with answering IRB stipulations to obtain final approval; documents IRB approval and contract approval.

  • Under direction of PI may draft various communications with Sponsor and/or regulatory documents to be sent to the Sponsor.

  • May assist PI and/or research nurse coordinator in the planning and design of source documents for protocol.

  • Assists in developing procedures for laboratory collection and storage.

  • Assists in processing and shipping lab specimens; retrieves and/or sends identified research specimens certified if indicated as per regulations.

  • Assists in precepting new clinical research staff and educating other research staff regarding scientific aspects of studies.

  • Assists in processing and shipping lab specimens efficiently and cost effectively; maintains supply inventory and equipment; maintains regulatory standards.

  • Assists with the budget development; may monitor ledgers.

  • Adheres to internal controls established for department.

  • May assist PI in obtaining Informed Consent from study participant and documents appropriately.

  • Adheres to internal controls and reporting structure.

MARGINAL OR PERIODIC JOB FUNCTIONS:

  • If appropriately trained and tested for competency, obtains Vital Signs and performs phlebotomy; monitors participants’ labs and notifies the PI of laboratory findings.

  • May attend and participate in the Investigator meeting

  • Performs related duties as required.

REQUIRED EDUCATION / EXPERIENCE:

Bachelor’s degree or equivalent, and two years of directly related experience.

Salary Range:

$44,320-$55,400 Commensurate with Experience.

EQUIPMENT:

Standard office equipment.

WORKING ENVIRONMENT/LOCATION OF POSITION:

Standard hospital, clinical, laboratory and/or office environments.

Equal Employment Opportunity

UTMB Health strives to provide equal opportunity employment without regard to race, color, religion, age, national origin, sex, gender, sexual orientation, gender identity/expression, genetic information, disability, veteran status, or any other basis protected by institutional policy or by federal, state or local laws unless such distinction is required by law. As a VEVRAA Federal Contractor, UTMB Health takes affirmative action to hire and advance women, minorities, protected veterans and individuals with disabilities.

Compensation

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