Clinical Research Coordinator I

Apply now (https://secure.dc4.pageuppeople.com/apply/674/gateway/default.aspx?c=apply&lJobID=533135&lJobSourceTypeID=796&sLanguage=en-us) Job no: 533135

Work type: Staff Full-Time

Location: Jacksonville Campus

Categories: Grant or Research Administration, Health Care Administration/Support

Department: 30010100 - JX-DEAN-ADMINISTRATION

Classification Title:

Clinical Research Coordinator I

Job Description:

Submission of protocol, and consent documents for IRB approval and assist in preparing regulatory submissions as requested Obtain informed consent; communicate with potential study participants through community lectures, health fairs, etc.; and participant retention as needed. Work closely with the department leadership and other study staff to determine study participant eligibility. Review eligibility and recruitment material; provide and explain enrollment information to research participants. Conduct study visits for multiple protocols and follow-ups including functions necessary for successful completion. Follow-up with study Principal Investigator and Clinical Research Manager on any participant adverse events (AEs) and serious adverse events (SAEs).

Work at UF research locations prescreening, consenting, and enrolling participants in research studies

Coordinates and implements enrollment and follow-up procedures to collect data from patient charts, medical records, interviews, questionnaires, and other sources.

Perform blood draws as needed at various time points in clinical trials. Assess and report patient reactions to clinical staff and PI. Perform vitals, collect specimens, and provide patient care per study protocol. Manages tests, procedures, and equipment per protocol requirements. Process blood samples in the biomedical lab

Package and ship biospecimens to the appropriate site

Help Investigators with progress reports, regulatory paperwork, and study files.

Serve as a backup for master research participant schedule coordination, notification of necessary parties, greeting, and check-in/check-out participants. Perform phone screening and documentation, data entry and IRB-related clerical duties. May make reminder calls and send reminder letters to study participants.

Update participant tracking logs as needed. Serve as back-up to answer the main phone line and assist with front desk duties.

Other duties as assigned by CRO/ORA leadership

Expected Salary:

$43,888- $50,000

Minimum Requirements:

Associates degree or an allied health professional degree in an appropriate area and one year of relevant experience; or an equivalent combination of education and experience.

Preferred Qualifications:

Bachelor’s degree or an allied health professional degree in an appropriate area and one year of relevant experience; or an equivalent combination of education and experience.

Experience in phlebotomy and clinical research is preferred.

Excellent interpersonal skills and the ability to prioritize and effectively communicate verbally

and in writing. Bilingual (English and Spanish) ability.

Coordinates multiple tasks and works independently and productively in a fast-paced, deadline-oriented environment.

This position requires proficiency in data management and superior organizational skills.

Integrity, careful attention to detail; ability to maintain confidentiality, demonstrate professionalism and respect for subjects’ rights and individual needs; willingness to learn and maintain skills per HIPAA regulations and Good Clinical Practice guidelines.

Special Instructions to Applicants:

In order to be considered, you must upload your cover letter and resume.

Application must be submitted by 11:55 p.m. (ET) of the posting end date.

Health Assessment Required:Yes

Advertised: 13 Sep 2024 Eastern Daylight Time

Applications close: 27 Sep 2024 Eastern Daylight Time