Top 48 Clinical research coordinator Jobs in Boca Raton Fl

Clinical Research Coordinator-FT
Evolution Research Group —Delray Beach, FL
- Full-time
- Mid-level
- High school diploma or GED
- Neurology
- Health insurance
- Dental insurance
Quick Apply
Quality Assurance Coordinator (Clinical Research)
Research Centers of America —Hollywood, FL
- Full-time
- Background check
- Spanish
- Psychiatry
- Health savings account
- Health insurance
Quick Apply
Clinical Research Coordinator
Segal Institute for Clinical Research —Boynton Beach, FL
- Full-time
- Vital signs
- Research
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
Clinical Research Coordinator (Phlebotomy)
Segal Institute for Clinical Research —Lauderhill, FL
- Full-time
- Vital signs
- Psychiatry
- Addiction Medicine
- Health insurance
- Dental insurance
Quick Apply
Clinical Research Coordinator I/II/III Opportunities – Multiple Locations Nationwide
Headlands Research —Lake Worth, FL
- $45,000 - $100,000 a year
- Bachelor's degree
- Psychology
- Communication skills
Quick Apply
Clinical Research Coordinator 1
University of Miami —Boca Raton, FL
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Bachelor's degree
- Health insurance
- Dental insurance
Clinical Research Coordinator
BRCR Global —Plantation, FL
- Full-time
- Background check
- English
- In-person
- 401(k)
- Paid time off
Quick Apply
11h
Clinical Mental Health Counseling Clinical Coordinator - FT40 (remote)
Keiser University —Fort Lauderdale, FL
- Weekends as needed
- Remote
- Master's degree
- Senior level
- 4 years
Quick Apply
Clinical Support Coordinator - FT Nights
Holy Cross Hospital —Fort Lauderdale, FL
- 12 hour shift
- High school diploma or GED
- Computer skills
- Communication skills
1d
Clinical Research Coordinator
Atlas Essentials —Delray Beach, FL
- Full-time
- Background check
- Microsoft Excel
- Vital signs
Quick Apply
15h
Clinical Research Coordinator
Headlands Research —Lake Worth, FL
- Full-time
- Spanish
- Laboratory experience
- English
- Health savings account
- Paid holidays
Clinical Intake Coordinator/scheduler
Reliance Home Health Care —West Palm Beach, FL
- $20 - $25 an hour
- Full-time
- HIPAA
- Administrative experience
- Organizational skills
- Health insurance
- 401(k)
Quick Apply
11h
Medical Assistant (Clinical Research)
Research Centers of America —Hollywood, FL
- Spanish
- Computer literacy
- Writing skills
- Health insurance
- Dental insurance
Quick Apply
Regional Travel, Clinical Research Coordinator
Care Access —Tamarac, FL
- $75,000 - $105,000 a year
- Microsoft Word
- Vital signs
- Computer literacy
- Health savings account
- Paid holidays
10d
Clinical Research Associate III - 991369
Nova Southeastern University —Fort Lauderdale, FL
- Full-time
- Background check
- 5 years
- Writing skills
- Health insurance
- Dental insurance
Clinical Support Coordinator (Unit Secretary) - ER Deerfield Beach
Holy Cross Hospital —Fort Lauderdale, FL
- 12 hour shift
- High school diploma or GED
- Computer skills
- ER
- Health insurance
- Dental insurance
Site Manager – Clinical Research (Neuroscience & Psychedelics)
Segal Trials —Lauderhill, FL
- Full-time
- Psychiatry
- 3 years
- Supervising experience
- Health insurance
- Dental insurance
Quick Apply
Clinical Research Assistant / Medical Assistant
CenExel Clinical Research —Hollywood, FL
- Full-time
- Background check
- Spanish
- Vital signs
- Health savings account
- Health insurance
Quick Apply
Physical Therapist Rehab Clinical Coordinator
Revival Home Health Care —Margate, FL
- Full-time
- Background check
- Physical & Rehabilitation Medicine
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
3d
Patient Recruitment Manager (Clinical Research)
CenExel Clinical Research —Hollywood, FL
- Full-time
- Background check
- Spanish
- Management
- Health savings account
- Health insurance
Quick Apply

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Clinical Research Coordinator-FT

Evolution Research Group -
Delray Beach, FL

Quick Apply

Job Details

Full-time

Benefits

Health insurance
Dental insurance
Paid time off
401(k) matching

Qualifications

Computer operation
High school diploma or GED
ICH guidelines
Research regulatory compliance
Clinical quality assurance standards
FDA regulations

Full Job Description

About Company:

Evolution Research Group (ERG) is dedicated to delivering high-quality Phase I–IV clinical trial execution to help sponsors bring lifesaving and life-enhancing therapies to market quickly and safely. Founded in 2014, ERG has grown into a leading neuroscience clinical development company, with affiliate sites across the U.S. and deep expertise in clinical pharmacology, psychiatry, neurology, acute pain, and metabolic disorders. ERG has completed over 5,000 trials and continues to expand into high-need therapeutic areas in the U.S. and globally.

Why join us? We offer a supportive culture, meaningful work, and the opportunity to contribute to cutting-edge research alongside industry leaders. Plus, we offer competitive benefits include medical and dental coverage, a matching 401(k), and paid time off to recharge.

Job Description:

The Clinical Research Coordinator is responsible for the overall coordination, organization, management, and efficient implementation of clinical trials. The CRC completes all study related procedures and distributes study medication and instructions to research subjects under the direction of the Principal Investigator and the Site Director. They maintain accurate, confidential files and documentation of study participants. In executing these position responsibilities, the Clinical Research Coordinator is guided by FDA regulations, Good Clinical Practice (GCP), and company standard operating procedures and policies.

Responsibilities:

General

Obtain detailed knowledge of all components of each study protocol through review and analysis of study information with Principal Investigator and Site Director prior to the effective date of the study.
Assist to develop draft source documents and review the documents for accuracy and clarity prior to study start up.
Review with Principal Investigator and Site Director, any components of the study for which additional information or clarification are required prior to the initiation of the study.
Manage studies with direct oversight from Site Director, and Principal Investigator to ensure compliance with protocol requirements.
Manage studies with Principal Investigator, Site Director, and Recruitment Manager to develop effective programs for study enrollment.
Contribute to the SOP review and development as delegated by the Site Director.

Study Management

Perform study activities as delegated by the Principal Investigator and under the supervision of the Site Director.
Attend the investigator meeting for each assigned protocol, as appropriate with directive from Site Director.
In conjunction with Site Director and Principal Investigator, ensure adherence to the protocols and document breaches or violations with sponsors and appropriate Institutional Review Boards (IRBs) and other outside regulatory organizations, as required.
Screen, enroll subjects and schedule subject visits in conjunction with Principal Investigator
Review and obtain informed consent from with potential study volunteer
Document all written and phone correspondences with sponsor, labs, IRB other regulatory organizations
Maintain organized, accurate and complete study records
Assist Principal Investigator in conducting studies in manner to ensure integrity of data and safety of subjects.
Enter data as appropriate for protocol (paper-electronic data capture)
In conjunction with Principal Investigator, accurately report and track adverse events as defined by each study protocol.
Perform study close-out procedures.
Store study records appropriately
Additionally, this role may encompass responsibilities beyond those outlined above, as required by the evolving needs of the organization. This job description is intended as a foundation and may be subject to expansion or modification to best suit ERG’s objectives.

Skills and Qualifications:

Education and experience
- High School Diploma or its equivalent; College degree preferred.
- Able to communicate with providers, co-workers, sponsors, and others in a collaborative and courteous manner.
- 1-2 years of clinical research experience preferred.
- Knowledgeable in medical terminology to communicate with physician office and laboratory staff.
- Demonstrate the initiative to act independently, initiate activity as required and make appropriate decisions within the constraints of study protocols, regulatory requirements, and company policy.
- Able to initiate or modify behavior to achieve desired outcomes in spite of environmental factors, priorities, or problems that might not be well defined or that are subject to change.
Requirements
- Understand regulatory requirements, as well as Good Clinical Practices (GCP) and International Conference of Harmonization (ICH) guidelines.
- Excellent communication skills (interpersonal, written, verbal)
- Basic computer skills to include Word, Excel, as well as proprietary applications unique to the clinical research industry (such as Study Manager)

Quick Apply

Refine Your Search

clinical research coordinator jobs in boca raton fl

Clinical Research Coordinator-FT

Quality Assurance Coordinator (Clinical Research)

Clinical Research Coordinator

Clinical Research Coordinator (Phlebotomy)

Clinical Research Coordinator I/II/III Opportunities – Multiple Locations Nationwide

Clinical Research Coordinator 1

Clinical Research Coordinator

Clinical Mental Health Counseling Clinical Coordinator - FT40 (remote)

Clinical Support Coordinator - FT Nights

Clinical Research Coordinator

Clinical Research Coordinator

Clinical Intake Coordinator/scheduler

Medical Assistant (Clinical Research)

Regional Travel, Clinical Research Coordinator

Clinical Research Associate III - 991369

Clinical Support Coordinator (Unit Secretary) - ER Deerfield Beach

Site Manager – Clinical Research (Neuroscience & Psychedelics)

Clinical Research Assistant / Medical Assistant

Physical Therapist Rehab Clinical Coordinator

Patient Recruitment Manager (Clinical Research)

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