Top 79 Clinical research coordinator Jobs in Tampa, Fl

Clinical Research Coordinator
Comprehensive Hematology Oncology —Saint Petersburg, FL
- $20 - $23 an hour
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Computer literacy
- Health insurance
- Dental insurance
Quick Apply
Clinical Research Coordinator
BayCare —Tampa, FL
- Full-time
- Hospital
- 5 years
- HIPAA
- Health insurance
- Dental insurance
8d
Clinical Research Coordinator I - Heme | Myeloid
Moffitt Cancer Center —Tampa, FL
- $26.32 - $40.14 an hour
- Full-time
- Hybrid work
- Psychology
- Business Administration
- Business
- Paid training
- Relocation assistance
4d
CLINICAL RESEARCH COORDINATOR I
Moffitt Cancer Center —Tampa, FL
- Full-time
- Hybrid work
- Psychology
- Business Administration
- Social Work
- Paid training
- Relocation assistance
CLINICAL RESEARCH COORDINATOR ASSOCIATE
Moffitt Cancer Center —Tampa, FL
- $21.12 - $32.24 an hour
- Full-time
- Hybrid work
- Word processing
- High school diploma or GED
- Business Administration
11d
Clinical Research Coordinator II
Johns Hopkins All Children's Hospital —Saint Petersburg, FL
- Full-time
- Nursing
- Mid-level
- Bachelor's degree
Clinical Research Regulatory Coordinator (Brandon, Florida)
Cardiovascular Associates of America —Brandon, FL
- Full-time
- Remote
- Mid-level
- Continuous improvement
- Associate's degree
Quick Apply
Clinical Research Coordinator
United Digestive —Tampa, FL
- Full-time
- BLS Certification
- Pass drug screening
- HIPAA
Quick Apply
Clinical Research Coordinator
Alcanza Clinical Research —Clearwater, FL
- Full-time
- Spanish
- LVN
- HIPAA
- Health savings account
- Disability insurance
Quick Apply
Clinical Research Assistant/Research Support Specialist
University of South Florida —Tampa, FL
- Full-time
- Background check
- Vital signs
- Mid-level
- Health insurance
- Dental insurance
12d
Clinical Research Associate
University of South Florida —Tampa, FL
- Full-time
- HIPAA
- Mid-level
- Master's degree
- Health insurance
- Dental insurance
7d
CLINICAL TRIALS SCREENING COORDINATOR I
Moffitt Cancer Center —Tampa, FL
- Full-time
- Hybrid work
- Clinic
- 2 years
- Entry level
- Paid training
- Relocation assistance
NTRO RESEARCH COORDINATOR II
Moffitt Cancer Center —Tampa, FL
- $22.74 - $34.68 an hour
- Full-time
- Hybrid work
- No experience needed
- Mid-level
- Master's degree
- Dental insurance
- Paid time off
7d
MYEOMA & LYMPHOMA RESEARCH DATA COORDINATOR III
Moffitt Cancer Center —Tampa, FL
- $24.45 - $37.31 an hour
- Full-time
- Mid-level
- High school diploma or GED
- Associate's degree
12d
RESEARCH DATA COORDINATOR II - CUTANEOUS
Moffitt Cancer Center —Tampa, FL
- $22.74 - $34.68 an hour
- Full-time
- Word processing
- Mid-level
- 3 years
5d
Research Data Coordinator II - Immune Cell Therapy
Moffitt Cancer Center —Tampa, FL
- $22.74 - $34.68 an hour
- Full-time
- Word processing
- Mid-level
- 3 years
6d
Clinical Research Infusion Rn I
Moffitt Cancer Center —Tampa, FL
- $35.05 - $52.56 an hour
- Full-time
- Nursing
- Patient monitoring
- RN License
13d
EPIC RESEARCH TOOLS CLINICAL APPLICATIONS ANALYST II
Moffitt Cancer Center —Tampa, FL
- $87,092.20 - $132,717.00 a year
- Full-time
- Remote
- System design
- Mid-level
- 3 years
Clinical Nurse Coordinator RN Med Surg
HCA Florida St. Petersburg Hospital —Saint Petersburg, FL
- Full-time
- Surgery
- Mid-level
- Medical-Surgical
- Employee stock purchase plan
- Disability insurance
Quick Apply
RN Clinical Nurse Coordinator Operating Room
HCA Florida Largo Hospital —Largo, FL
- Full-time
- Surgery
- Mid-level
- Employee stock purchase plan
- Disability insurance
Quick Apply

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Clinical Research Coordinator

Comprehensive Hematology Oncology
Saint Petersburg, FL

Quick Apply

Job Details

Full-time
$20 - $23 an hour

Benefits

Health insurance
Dental insurance
401(k)
Tuition reimbursement
Paid time off
Vision insurance
401(k) matching
Life insurance

Qualifications

Computer operation
Teamwork
Microsoft Excel
Microsoft Outlook
Computer literacy
High school diploma or GED
Attention to detail
Data entry

Full Job Description

Position Summary

The Clinical Research Coordinator plays a vital role in supporting oncology and hematology clinical trials by ensuring accurate, timely, and compliant entry of clinical research data. This position is responsible for abstracting data from electronic medical records (EMR) and source documents and entering it into Electronic Data Capture (EDC) systems for multiple research studies. All activities are conducted under the supervision of the Principal Investigator (PI) and in accordance with federal regulations, sponsor requirements, and organizational policies.

Essential Duties and Responsibilities

Data Management & Entry

· Accurately enter clinical trial data into assigned EDC systems for multiple oncology and hematology research studies.

· Collect and abstract data from Electronic Medical Records (EMR), source documents, labs, imaging reports, and provider notes.

· Enter all study visit data into EDC systems within 48 hours of the participant visit.

· Organize, analyze, cross‑check, and validate data to ensure accuracy and completeness.

· Respond to sponsor queries and data clarification requests in a timely and professional manner.

Protocol & Compliance

· Review, understand, and adhere to study protocols, study schedules, and case report form requirements.

· Ensure research activities are conducted in compliance with federal regulations, Good Clinical Practice (GCP), sponsor guidelines, and internal SOPs.

· Support monitoring visits, audits, and inspections by maintaining organized and accurate data documentation.

· Report identified protocol deviations or potential non‑compliance issues to appropriate leadership.

Adverse Event & Safety Reporting

· Grade adverse events using the CTCAE (Common Terminology Criteria for Adverse Events) system.

· Identify and report qualifying Serious Adverse Events (SAEs) to the Regulatory Department for timely submission.

· Assist with maintaining accurate safety documentation within study records.

Communication & Collaboration

· Communicate with physicians, nurses, hospitals, and outside clinics to obtain missing data or verify information accuracy.

· Collaborate closely with research coordinators, regulatory staff, and clinical teams to support study operations.

· Maintain patient confidentiality and data integrity at all times.

Additional Responsibilities

· Adhere to research workflows, timelines, and productivity expectations.

· Participate in research team meetings, training, and ongoing education.

· Perform other research‑related duties as assigned.

Required Qualifications

· High school diploma or equivalent required

· Strong computer skills and attention to detail

· Proficiency with Microsoft Office (Excel, Word, Outlook/Email)

· Excellent written and verbal communication skills

· Ability to manage multiple tasks and meet deadlines in a fast‑paced environment

· Professionalism, reliability, and ability to work independently and as part of a team

Preferred Qualifications

· Prior experience in clinical research, oncology, hematology, or healthcare

· Experience working with EMR systems

· Experience with Electronic Data Capture (EDC) systems

· Familiarity with clinical trial processes, GCP, or regulatory standards

Work Environment

· Clinical research and medical office setting

· Frequent computer use and data entry

· Interaction with clinical staff, providers, and research sponsors

· May require sitting, standing, and occasional lifting of files or supplies

Why Join Comprehensive Hematology Oncology Group?

· Be part of meaningful cancer research that directly impacts patient care

· Support innovative treatments and clinical trials

· Work in a collaborative, mission‑driven, and supportive environment

· Opportunities for growth within clinical research operations

Job Type: Full-time

Pay: $20.00 - $23.00 per hour

Benefits:

401(k)
401(k) matching
Dental insurance
Health insurance
Life insurance
Paid time off
Tuition reimbursement
Vision insurance

Education:

High school or equivalent (Preferred)

Work Location: In person

Quick Apply

Refine Your Search

clinical research coordinator jobs in tampa, fl

Clinical Research Coordinator

Clinical Research Coordinator

Clinical Research Coordinator I - Heme | Myeloid

CLINICAL RESEARCH COORDINATOR I

CLINICAL RESEARCH COORDINATOR ASSOCIATE

Clinical Research Coordinator II

Clinical Research Regulatory Coordinator (Brandon, Florida)

Clinical Research Coordinator

Clinical Research Coordinator

Clinical Research Assistant/Research Support Specialist

Clinical Research Associate

CLINICAL TRIALS SCREENING COORDINATOR I

NTRO RESEARCH COORDINATOR II

MYEOMA & LYMPHOMA RESEARCH DATA COORDINATOR III

RESEARCH DATA COORDINATOR II - CUTANEOUS

Research Data Coordinator II - Immune Cell Therapy

Clinical Research Infusion Rn I

EPIC RESEARCH TOOLS CLINICAL APPLICATIONS ANALYST II

Clinical Nurse Coordinator RN Med Surg

RN Clinical Nurse Coordinator Operating Room

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