Clinical Research Coordinator (Masked)

Medix; Florida; On-site; USD 60,000 - 68,000; Full time

Benefits offered by this job

Full benefits

Job summary

Medix in Florida is seeking a Clinical Research Coordinator to support phase 2 and 3 trials at a Wildwood site. You will coordinate subject visits, prepare documentation, ensure data accuracy in electronic CRFs, and assist with ECGs and adverse event reporting, among other duties.

The role offers a strong team culture, growth opportunities within a national organization, and a comprehensive benefits package.

Job description

Clinical Research Coordinator (Masked) (257288) Wildwood, Florida

Salary: USD60000 - USD68000 per year + Full benefits

We are looking for a talented research focused individual to join our growing team. As part of a larger national organization, we have a great local site level culture with the opportunity for tons of growth throughout your career. If you are looking to join an organization with a lot of upward mobility, strong company culture, and a great work life balance, this role is for you.

Duties:

• Coordinate and schedule subject visits within study/subject specific windows per protocol guidelines.
• Prepare visit-specific documentation and charts for Clinical Research Coordinator
• Observe Coordinator in patient care and management
• Assist Coordinator in monitoring subject flow and assist in subject care and management
• Observe, assist, collect and record all necessary data for follow up (e.g. adverse events, concomitant medications, etc.) study visits (Phase 2 & 3; NO Gene Therapy)
• Transcribe subject study information from source documents to the Electronic Case Report Forms
• Administer all mandatory questionnaires to study subjects
• Set up, prepare subject, and conduct electrocardiograms (ECG) on subjects as required per study protocol
• Promptly request all necessary medical records for Serious Adverse Event Reporting
• Process and ship laboratory biological samples for analysis
• Perform intraocular pressure checks after injections
• Perform trial frame refraction and ETDRS visual acuity testing (For ISTs only, at selected sites)
• Inform subjects and obtain written re-consents in regard to ICF’s
• Perform other duties as assigned
• Obtain any applicable additional/required sponsor training and/or certifications