Clinical Research Coordinator II - Onsite Study Lead

1459 Illingworth Research Group (USA) Inc.

Miami (FL)

On-site

USD 65,000 - 90,000

Full time

7 days ago
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Benefits offered by this job

Company car or car allowance
Health benefits
401k match
Employee Stock Purchase Plan
Bonus eligibility
Flexible PTO and sick time

Job summary

1459 Illingworth Research Group (USA) Inc. in Miami, FL is seeking a Clinical Research Coordinator to support multi-site trials.

The role covers start-up activities, regulatory documentation, site files, patient scheduling, data entry, and coordination with the PI. Travel up to 100% and flexible schedules may be required.

You will ensure GCP compliance, manage Case Report Forms, monitor AE/SAE, and assist with audits while maintaining TMF and study files.

Qualifications

  • Registered Nurse and/or University Degree such as Bachelor of Science Degree required.
  • Clinical Research certification preferred.
  • A minimum of 1 year experience in clinical research required, 2+ years preferred.
  • Knowledge of regulations, ICH GCP, privacy, and applicable guidelines.
  • Problem solving, planning, and evaluation skills.
  • Good time management, detail-oriented, and able to multi-task.
  • Good interpersonal and communication skills with a team focus.
  • Knowledge of SOP writing.
  • Ability to anticipate problems and provide timely solutions.
  • Ability to coordinate multiple clinical research projects with competing deadlines.
  • Proficiency in Word, Excel, PowerPoint.
  • Proficiency in use of various clinical trial EDC software preferred.
  • CRC II onsite support one day per week for 6–8 weeks, then 1–2 visits per month.

Responsibilities

  • Review and prepare trial documents and TMF for the study.
  • Coordinate start-up activities including clinic logistics and training.
  • Monitor regulatory documentation and communicate with auditors.
  • Support PI with delegation log, scheduling, and monitor visits.
  • Manage daily tasks and visit calendars; enrollment and follow-up.
  • Travel up to 100% as required.

Skills

Registered Nurse
Coordination
GCP Knowledge
Multitasking

Education

RN License
BSN preferred

Tools

EDC Software
MS Word/Excel/PP

Job description

1459 Illingworth Research Group (USA) Inc. in Miami, FL is seeking a Clinical Research Coordinator to support multi-site trials.

The role covers start-up activities, regulatory documentation, site files, patient scheduling, data entry, and coordination with the PI. Travel up to 100% and flexible schedules may be required.

You will ensure GCP compliance, manage Case Report Forms, monitor AE/SAE, and assist with audits while maintaining TMF and study files.

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