Clinical Research Coord III Position Available In Alachua, Florida

Clinical Research Coord III

JOB NO:

536186

WORK TYPE:

Staff Full-Time

LOCATION

Main Campus (Gainesville, FL)

CATEGORIES

Office/Administrative/Fiscal Support, Grant or Research Administration, Health Care Administration/Support

DEPARTMENT

29050903

• MD-PULMONARY-OTHER

CLASSIFICATION TITLE:

Clinical Research Coordinator III
CLASSIFICATION

MINIMUM REQUIREMENTS

Bachelor’s degree in an appropriate area and three years of relevant experience; or an equivalent combination of education and experience.

JOB DESCRIPTION

The Department of Medicine, Division of Pulmonary is seeking a full time Clinical Research Coordinator III. This position will function independently in a clinical research setting and will be responsible for the complete coordination of assigned clinical research activities. The incumbent may have supervisory responsibilities and must demonstrate effective problem solving, writing and communication skills. The incumbent will lead clinical trials/clinical research within the Division of Pulmonary, Critical Care & Sleep Medicine and ensure compliance with federal, state and university policies.
Essential Functions;

• Clinical Trial Project Management
  Support the Alpha-1 Research Laboratory under the direction of Dr.

Karina Serban with industry sponsored clinical trials or internally funded clinical research. Screen daily/weekly to enroll patients into clinical trials. Coordinate with Clinical Research Center, inpatient unit or inpatient auxiliaries to schedule patients for study visits. Visit frequently with the study monitor to ensure compliance with industry protocol guidelines. Process patient stipends. Assist the Associate Program Director with any internal/external audits. Attend industry sponsored investigator meetings to gather updates on protocol changes, upcoming amendments, etc. Respond to any new industry sponsored solicitations. Regularly review research study billing to ensure compliance.

• Clinical trial regulatory management
  Prepare all CRH paperwork needed for study startup approval. Prepare IRB paperwork needed for study startup. Obtain CRH or IRB approval related to amendments, protocol changes, etc. Comply with all institutional, federal, state, sponsor and Divisional policies. Retain records/archive documents after study close out
• Clinical Trials budget
  Assist Dr. Serban with industry sponsored budget proposals. Obtain cost of services for all procedures, study visits, etc. related to trial.
• This position will perform ad hoc assignments as assigned by the Supervisor

EXPECTED SALARY

$53,000

• $76,500 Annually

REQUIRED QUALIFICATIONS

Bachelor’s degree in an appropriate area and three years of relevant experience; or an equivalent combination of education and experience.

PREFERRED

Five years of relevant Pulmonary clinical trial experience. Certified in Spirometry. Regulatory IRB and/or nursing degree a plus.

SPECIAL INSTRUCTIONS TO APPLICANTS

In order to be considered, you must upload your resume.
Application must be submitted by 11:55 p.m. (ET) of the posting end date.

HEALTH ASSESSMENT REQUIRED

Yes

ADVERTISED

16 Jun 2025

APPLICATIONS CLOSE:

23 Jun 2025 Whatsapp Facebook LinkedIn Email App