Clinical Research Coordinator, Sealy Center on Aging (Partial Remote, Onsite As Needed)

Clinical Research Coordinator, Sealy Center on Aging (Partial Remote, Onsite As Needed)

Galveston, Texas, United States

Clerical & Administrative Support

UTMB Health

Requisition # 2402330

Minimum Qualifications:

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

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:

• 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.

• Conducts behavioral intervention visits in the clinic setting.

• 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.

• Work with research databases to collect milestone research visits and develop reports. RED Cap database knowledge a plus.

• 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

• Knowledgeable of IRB practices e.g., submitting a protocol amendment, protocol deviation, and continuing review.

• 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 data collection and storage.

• Assists in processing and sharing data per data use agreements or if indicated asper regulations.Experience working with outside reporting agencies such as CROMS ~~~ a plus.

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

• 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.

• 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.

Salary Range:

$44,320 - $55,400.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 VEVRAA Federal Contractor, UTMB Health takes affirmative action to hire and advance women, minorities, protected veterans and individuals with disabilities.

Compensation