Clinical Research Coordinator | Four-Day Week & Impact

ADP, Inc.; Florida; On-site; USD 50,000 - 70,000; Full time

Benefits offered by this job

4-day work week

Competitive benefits

401(k) with employer match

Paid time off

Job summary

K2 Medical Research is seeking Clinical Research Coordinators to support our Orlando (Maitland), FL clinic as part of evergreen opportunities. We prioritize patient-centered, compliant conduct of multi-phasic trials across therapeutic areas and seek mission-driven professionals to join our team.

As a fast-growing CRO, you will ensure quality data collection, follow GCP guidelines, and collaborate with investigators, sponsors, and site staff to advance clinical trials.

Qualifications

• Direct experience working at a clinical research site.
• Bachelor’s degree strongly preferred; HS Diploma or GED required.

Responsibilities

• Understand assigned studies by reading protocols and coordinating with Principal Investigator.
• Adhere to study protocol and obtain exemptions when appropriate.
• Communicate protocol issues to CRO/Sponsor and study staff.
• Collect initial psychiatric and medical information by interviewing patients.
• Maintain source documentation and sponsor data.
• Dispense and manage study medication records.

Skills

Clinical research experience

Communication skills

Interpersonal skills

Mentoring relationships

Education

HS Diploma or GED

Bachelor’s degree preferred

Job description

K2 Medical Research is seeking Clinical Research Coordinators to support our Orlando (Maitland), FL clinic as part of evergreen opportunities. We prioritize patient-centered, compliant conduct of multi-phasic trials across therapeutic areas and seek mission-driven professionals to join our team.

As a fast-growing CRO, you will ensure quality data collection, follow GCP guidelines, and collaborate with investigators, sponsors, and site staff to advance clinical trials.