Top 12 Clinical research associate Jobs in Jupiter Fl

Clinical Research Coordinator
Medix —Lake Worth, FL
- $70,000 - $80,000 a year
- Full-time
- Background check
- Spanish
- English
Quick Apply
5h
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
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Research Regulatory Affairs Specialist I
Florida Cancer Specialists & Research Institute —West Palm Beach, FL
- Full-time
- Background check
- Microsoft Outlook
- Customer service
- Tuition reimbursement
- 401(k) matching
Clinical Trials Site Director – Multiple Locations Nationwide
Headlands Research —Lake Worth, FL
- Senior level
- Leadership
Quick Apply
RN or LPN Clinical Research Coordinator
Cardiovascular Associates of America —Palm Beach Gardens, FL
- Full-time
- Mid-level
- Office
- Bachelor's degree
- Flexible schedule
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Site Manager, Clinical Research
Health Haven —West Palm Beach, FL
- $60,000 - $80,000 a year
- Full-time
- Background check
- Nursing
- Mid-level
- Paid holidays
- Disability insurance
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4d
Clinical Research Coordinator
Headlands Research —Lake Worth, FL
- Full-time
- Spanish
- Laboratory experience
- English
- Health savings account
- Paid holidays

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Clinical Research Coordinator

Medix -
Lake Worth, FL

Quick Apply

Job Details

Full-time
$70,000 - $80,000 a year
5 hours ago

Qualifications

Care documentation
High school diploma or GED
ICH guidelines
Clinical assessment documentation
Clinical quality assurance standards
Clinical documentation standards
Medical terminology
FDA regulations

Full Job Description

Responsibilities

Coordinate all aspects of assigned clinical trials from site initiation to study close-out
Conduct subject visits and ensure timely, accurate documentation following ALCOA-C standards
Maintain compliance with study protocols, GCP/ICH guidelines, FDA regulations, IRB policies, and company SOPs
Manage subject recruitment, informed consent, and retention strategies
Ensure timely data entry and resolution of EDC queries
Report and follow up on all adverse events, serious adverse events, and deviations
Collaborate with investigators, lab teams, sponsors/CROs, and internal stakeholders
Prepare for and participate in monitoring visits, audits, and inspections
Maintain regulatory documentation and ensure proper training is completed for all study amendments and systems
Execute study procedures such as phlebotomy, ECGs, and sample processing within scope (as trained)
Attend investigator meetings and provide cross-functional support as needed
Maintain working knowledge of study protocols, laboratory manuals, equipment calibration, and inventory control

Required Skills

Required: High school diploma or GED
Experience:
Minimum of 1 year of experience as a Clinical Research Coordinator OR
Minimum of 2 years of experience as a Research Assistant in Clinical Research
Deep understanding of FDA, ICH-GCP regulations, and clinical trial procedures
Proficiency in medical terminology and clinical documentation practices

Preferred Skills

Strong interpersonal, verbal, and written communication skills
Organized, detail-oriented, and capable of managing multiple priorities
Proficient in Microsoft Office and other clinical research systems
Bilingual (English/Spanish) is strongly preferred

Schedule/Shift

Type: Regular Full-time Employee

Schedule: Mondays through Fridays, 8:30am - 4:30pm

Location: Onsite in Lake Worth, FL (no capabilities for remote or hybrid work)

#MedixLS

For California Applicants:

We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable federal, state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance (FCIHO), Los Angeles Fair Chance Ordinance for Employers (ULAC), The San Francisco Fair Chance Ordinance (FCO) , and the California Fair Chance Act (CFCA).

This position is subject to a background check based on its job duties, which may include patient care, working with vulnerable populations, access to financial and confidential information, driving, working with heavy machinery, or working in a warehouse or laboratory environment. Due to these job duties, this position has a significant impact on the business operations and reputation, as well as the safety and well-being of individuals who may be cared for as part of the job position or who may interact with staff or clients.

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Refine Your Search

clinical research associate jobs in jupiter fl

Clinical Research Coordinator

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

Research Regulatory Affairs Specialist I

Clinical Trials Site Director – Multiple Locations Nationwide

RN or LPN Clinical Research Coordinator

Site Manager, Clinical Research

Clinical Research Coordinator

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