Top 22 Assistant clinical research coordinator Jobs in Orlando Fl

Clinical Research Coordinator
ClinTrial Research, INC —Orlando, FL
- $55,000 - $75,000 a year
- Full-time
- HIPAA
- Office
- Continuous improvement
- Health savings account
- Health insurance
Quick Apply
Clinical Research Coordinator
Cardiovascular Associates of America —Orlando, FL
- Full-time
- Mid-level
- Office
- Bachelor's degree
- Flexible schedule
Quick Apply
10d
Clinical Research Nurse Practitioner (APRN) or Physician Associate (PA-C)
Conquest Research —Winter Park, FL
- $100,000 - $120,000 a year
- Full-time
- Spanish
- Writing skills
- English
- Health insurance
- Dental insurance
Quick Apply
Pediatric Psychologist
Nemours —Orlando, FL
- Full-time
- Experience working with individuals with developmental disabilities
- Outpatient experience
- Doctor of Philosophy
- 403(b) matching
- Dental insurance
Clinical Research Coordinator II RN Oncology
AdventHealth Orlando Support —Altamonte Springs, FL
- $65,582.40 - $108,646.85 a year
- Full-time
- 18 years or older
- Spanish
- CPR Certification
- Paid parental leave
- Disability insurance
Research Nurse - Enrollment
Sarah Cannon Research Institute —Orlando, FL
- Full-time
- Nursing
- Vital signs
- RN License
9d
Clinical Assistant Nurse Manager-Neuro Trauma
Orlando Health —Orlando, FL
- Full-time
- Acute care
- Nursing
- Patient monitoring
Research Nurse - Enrollment
McKesson —Orlando, FL
- Nursing
- Vital signs
- RN License
- Wellness program
- Employee stock purchase plan
9d
Clinical Assistant Nurse Manager - Intensive Care Unit (Nights)
Orlando Health —Orlando, FL
- 12 hour shift
- Nursing
- Patient monitoring
- RN License
- Paid parental leave
- Loan repayment program
Clinical Assistant Nurse Manager - Progressive Care Unit / PCU
Orlando Health —Orlando, FL
- 12 hour shift
- Acute care
- Nursing
- Patient monitoring
- Paid parental leave
- Loan repayment program
Medical Assistant & Research Scheduler (CRC Support)
CENTRAL FLORIDA MEDICAL & CHIROPRACTIC CENTER, INC. —Winter Park, FL
- Full-time
- Background check
- Patient care
- 1 year
Quick Apply
Clinical Assistant Nurse Manager - Intermediate Critical Care / Multisystem PCU
Orlando Health —Orlando, FL
- 12 hour shift
- Acute care
- Nursing
- Patient monitoring
- Paid parental leave
- Loan repayment program
Clinical Assistant Nurse Manager - Eustis Freestanding Emergency Department
Orlando Health —Ocoee, FL
- 12 hour shift
- Nursing
- Patient monitoring
- RN License
Clin Assistant Nurse Mgr - Health Central ICU- Nights
Orlando Health —Ocoee, FL
- Full-time
- Nursing
- Surgery
- Patient monitoring
- Benefits from day one
7d
Lecturer, Health Sciences – Nutrition and Dietetics
University of Central Florida —Orlando, FL
- Online Application
- 5 years
- University
- Doctor of Philosophy
- Paid holidays
- Health insurance
5d
Clinical Assistant Nurse Manager - Post Anesthesia Care Unit at Lake Mary Hospital
Orlando Health —Lake Mary, FL
- Full-time
- Acute care
- Nursing
- Patient monitoring
- Tuition reimbursement
- Opportunities for advancement
8d
Clinical Assistant Nurse Manager - ED Unit - Day - VFT - Reunion Standalone ED
Orlando Health —Davenport, FL
- Full-time
- Nursing
- Patient monitoring
- RN License
Clinical Assistant Nurse Manager - REGISTERED NURSE - ORMC
Orlando Health —Orlando, FL
- Full-time
- Acute care
- Nursing
- Patient monitoring
Clinical Assistant Nurse Manager (RN) - ORMC Endoscopy - Full Time / First Shift
Orlando Health —Orlando, FL
- Full-time
- Acute care
- Nursing
- Patient monitoring
- Benefits from day one
5d
Charge Nurse RN - ORMC
Orlando Health —Orlando, FL
- Full-time
- Acute care
- Nursing
- Patient monitoring

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assistant clinical research coordinator jobs near orlando fl

Clinical Research Coordinator

ClinTrial Research, INC
Orlando, FL

Quick Apply

Job Details

Full-time
$55,000 - $75,000 a year

Benefits

Health savings account
Health insurance
Dental insurance
401(k)
Flexible spending account
Paid time off
Parental leave
Vision insurance
401(k) matching
Life insurance

Qualifications

HIPAA
Filing
Medical scheduling
Team development
Continuous improvement

Full Job Description

Position Summary:

The Clinical Research Coordinator (CRC) is an experienced, independent clinical execution role responsible for managing complex study activities, ensuring protocol compliance and data integrity, and serving as a senior resource within the site team. Reporting to the Site Manager and working closely with the Associate Director, Site Development, the CRC leads the full lifecycle of clinical trial conduct across multiple concurrent studies — from site activation and patient enrollment through study close-out. This role will operate out of one of two office locations: CTR Oakwater (Orlando, FL) and CTR Clermont (Clermont, FL). The CRC II serves as a mentor and functional lead for Junior staff, and partners with Regulatory, Patient Engagement, Commercial Strategy, and Site Operations teams to ensure CTR executes studies with precision and in full compliance with GCP, IRB, and sponsor requirements.

Key Responsibilities:

Patient Enrollment & Study Conduct

Lead patient screening, eligibility assessment, and enrollment activities across multiple concurrent protocols, exercising independent clinical judgment on complex eligibility determinations.
Oversee informed consent processes, ensuring full compliance with IRB-approved consent procedures and documenting exceptions or deviations appropriately.
Perform and/or supervise all study visit activities including dosing, drug administration, drug accountability, specimen collection and shipping, CTMS data entry, and patient record maintenance.
Monitor study activities for ongoing compliance with protocols, ICH-GCP standards, and applicable regulatory requirements; proactively identify and escalate compliance risks.
Track and manage enrollment status across assigned studies; document patient dropouts; record, report, and follow up on adverse events and protocol deviations in accordance with sponsor and regulatory requirements.
Serve as the primary site contact for sponsor representatives and CROs during monitoring visits and routine study communications.

Data Quality & Regulatory Compliance

Create, maintain, and quality-review source documents and study records in accordance with GCP, CTR SOPs, and sponsor requirements.
Build, manage, and audit study data in CTMS (RealTime), ensuring timely, accurate, and complete data entry across all active studies; identify and resolve data discrepancies prior to monitoring visits.
Adhere to all applicable SOPs, ICH-GCP guidelines, HIPAA requirements, and privacy regulations at all times.
Lead preparation for internal audits, sponsor monitoring visits, and regulatory inspections; serve as the primary point of contact for on-site monitors and ensure inspection-ready study files are maintained continuously.
Review and contribute to the development and revision of CTR SOPs and study-specific procedures as requested by the Site Manager or Quality team.

Study Start-Up & Business Development Support

Lead or co-lead site activation activities including IRB submissions, protocol training, system setup in CTMS, and regulatory document collection.
Complete feasibility questionnaires and support pre-award site visits, drawing on protocol-level expertise to provide accurate and competitive assessments.
Provide clinical and protocol intelligence to the Commercial Strategy and Site Development teams to support feasibility submissions and sponsor engagement.
Assist with budget and contract review by identifying protocol-driven visit and procedure requirements; escalate scope discrepancies to the Site Manager or CBO.

Team Leadership & Site Operations

Serve as a mentor and day-to-day resource for CRC I staff and Research Assistants; provide protocol-specific training, answer procedural questions, and escalate performance concerns to the Site Manager.
Coordinate with Patient Engagement, Regulatory & Quality, and Site Operations teams to ensure seamless patient scheduling, visit preparation, and study execution.
Support study close-out activities including final data reconciliation, regulatory binder completion, and sponsor communication.
Contribute to a culture of quality, accountability, and continuous improvement within the site team.

Pay: $55,000.00 - $75,000.00 per year

Benefits:

401(k)
401(k) matching
Dental insurance
Flexible spending account
Health insurance
Health savings account
Life insurance
Paid time off
Parental leave
Vision insurance

Work Location: In person

Quick Apply

Refine Your Search

assistant clinical research coordinator jobs in orlando fl

Clinical Research Coordinator

Clinical Research Coordinator

Clinical Research Nurse Practitioner (APRN) or Physician Associate (PA-C)

Pediatric Psychologist

Clinical Research Coordinator II RN Oncology

Research Nurse - Enrollment

Clinical Assistant Nurse Manager-Neuro Trauma

Research Nurse - Enrollment

Clinical Assistant Nurse Manager - Intensive Care Unit (Nights)

Clinical Assistant Nurse Manager - Progressive Care Unit / PCU

Medical Assistant & Research Scheduler (CRC Support)

Clinical Assistant Nurse Manager - Intermediate Critical Care / Multisystem PCU

Clinical Assistant Nurse Manager - Eustis Freestanding Emergency Department

Clin Assistant Nurse Mgr - Health Central ICU- Nights

Lecturer, Health Sciences – Nutrition and Dietetics

Clinical Assistant Nurse Manager - Post Anesthesia Care Unit at Lake Mary Hospital

Clinical Assistant Nurse Manager - ED Unit - Day - VFT - Reunion Standalone ED

Clinical Assistant Nurse Manager - REGISTERED NURSE - ORMC

Clinical Assistant Nurse Manager (RN) - ORMC Endoscopy - Full Time / First Shift

Charge Nurse RN - ORMC

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