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Clinical Research Coordinator, Ob/Gyn Research Support Unit (Galveston)

Job Description - Clinical Research Coordinator, Ob/Gyn Research Support Unit (Galveston)

Minimum Qualifications\: 

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

 

 

  • Preferred Qualifications\: 
     
  • Bilingual (Spanish/English) 
     
  • At least two (2) years of Medical Assistant experience, with hands-on experience performing phlebotomy.

 

 

Job Description:

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.

 

 

Job Duties\: 

The duties of this role will include but are not limited to the following:

  • 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 Process and ship lab specimens efficiently and cost effectively; maintains supply inventory and equipment; maintains regulatory standards. 
  • 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
  • Travel as needed to other clinics to administer consent to study participants, recruit participants or complete follow-up visits. 
  • May attend and participate in the Investigator meetings.
  • Performs related duties as required. 

 

 

Salary Range:
Commensurate with experience 
 


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 Federal Contractor, UTMB Health takes affirmative action to hire and advance protected veterans and individuals with disabilities.

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