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Remote Temporary Clinical Research Jobs in Florida

Careerxchange

Oncology CTMS Analyst

Miami, FL · Remote

$28 - $38/hr

This fully remote opportunity is ideal for an experienced Clinical Trials Management System (CTMS) professional with a strong background supporting oncology research operations, system optimization ...

IQVIA

Clinical Trial Psych Rater

Coral Gables, FL · Remote

$62K - $156K/yr

Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services ...

Danaher

Principal Clinical Scientist

Miami, FL · On-site +1

... remote based (can also be onsite in Chaska, MN). At Danaher Diagnostics, our vision is to be the ... Partner crossfunctionally with R&D, Regulatory, Medical Affairs, Quality, and Commercial teams to ...

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Remote Temporary Clinical Research information

What is the difference between Remote Temporary Clinical Research vs Remote Temporary Clinical Data Coordinator?

AspectRemote Temporary Clinical ResearchRemote Temporary Clinical Data Coordinator
CredentialsTypically requires a background in life sciences, clinical research certifications (e.g., CCRP), or related degreesRequires experience with data management, often with certifications like CDMP or related training
Work EnvironmentConducted remotely, often in research organizations or pharmaceutical companiesRemote data entry and management within clinical trial settings
Employer & Industry UsageUsed by biotech, pharma, and research institutions for trial oversightCommon in clinical research sites, CROs, and pharmaceutical companies for data handling

Remote Temporary Clinical Research involves overseeing or supporting clinical trials, requiring scientific knowledge and regulatory understanding. In contrast, Remote Temporary Clinical Data Coordinators focus on managing and entering trial data, emphasizing data accuracy and software skills. Both roles are remote, but they serve different functions within the clinical research process.

What are the most commonly searched types of Temporary Clinical Research jobs in Florida?

The most popular types of Temporary Clinical Research jobs in Florida are:

What are popular job titles related to Remote Temporary Clinical Research jobs in Florida?

For Remote Temporary Clinical Research jobs in Florida, the most frequently searched job titles are:

What job categories do people searching Remote Temporary Clinical Research jobs in Florida look for?

The top searched job categories for Remote Temporary Clinical Research jobs in Florida are:

What cities in Florida are hiring for Remote Temporary Clinical Research jobs?

Cities in Florida with the most Remote Temporary Clinical Research job openings:

Remote Temporary Clinical Research jobs near you
Infographic showing various Remote Temporary Clinical Research job openings in Florida as of August 2026, with employment types broken down into 94% Full Time, and 6% Part Time. Highlights an 100% Remote job distribution.

Senior Clinical Research Associate

ICON

Jacksonville, FL • On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 12 days ago

Job description

Senior Clinical Research Associate - Oncology - Jacksonville, FL
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
Responsibilities:
  • Perform site management activities to support the client's Oncology site success and maintain a continuous state of inspection readiness
  • Act as the primary contact and facilitate efficient communications between the client's clinical trial team and the sites
  • Perform remote and on-site monitoring/co-monitoring visits (Site Qualification Visits, Site Initiation Visits, Interim Monitoring Visits and Close-Out Visits) to ensure data integrity and subject safety in the client's trials
  • May perform oversight activities to assess monitoring quality and train/mentor less experienced CRAs
  • Promptly document monitoring activities and submit/approve visit reports
  • Manage site essential document collection and TMF reconciliation with site files
  • Support sites with local Institutional Review Board (IRB)/Ethics Committee (EC) submissions and confirm approvals
  • Regularly review site Key Risk Indicator (KRI) metrics, issues and action items to detect trends and ensure prompt resolution
  • Independently determine root causes and develop/implement site Corrective Action and Preventive Action (CAPA) plans
  • Deliver training to ensure sites comply with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs) and regulations
  • Support sites and the client's regulatory inspections
  • Contribute to site identification; drive site feasibility and qualification progress; and support site activation activities
  • Lead site engagement initiatives and foster relationships with key Oncology sites and networks

Qualifications
  • Bachelor's degree (scientific field preferred)
  • 5+ years monitoring clinical trials independently conducting on-site and remote monitoring visits. Atleast 2 years monitoring solid tumor clinical trials.
  • 1+ years early development oncology trial experience and/or Phase I or Phase III Oncology trial experience
  • Solid tumor clinical trial experience is required
  • Experience utilizing Veeva systems is highly preferred
  • Demonstrated experience developing/maintaining site relationships and securing compliance
  • Expertise in GxPs and Oncology monitoring techniques (including Risk-Based Monitoring) and terminology
  • Experience collaborating with sites from initial engagement through close-out phases
  • Experience activating sites
  • Experience training site staff
  • Experience supporting sites and/or sponsors in regulatory inspections
  • Experience working within a Functional Services (or in-house) monitoring model is preferred
  • Willing to travel up to 50%

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Are you a current ICON Employee? Please click here to apply

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