1

Endpoint Clinical Jobs in Florida (NOW HIRING)

Clinicia Expert - Remote

Miami, FL · Remote

$150 - $200/hr

Clinical Trial Evaluation * CTCAE Grading * RECIST * Lugano Criteria * IMWG Criteria * IWCLL Criteria * ELN Criteria * Outcome Endpoint Analysis (ORR, DoR, PFS, OS, MRD) * Dose Escalation Assessment

IT Manager - Healthcare

Oldsmar, FL · On-site

$87K - $106K/yr

Ensure reliable delivery of technology services supporting clinical, operational, and ... Oversee administration and support of Microsoft 365, Azure, Endpoint Management, Identity ...

Hematology Expert - Remote

Miami, FL · Remote

$150 - $200/hr

Clinical Trial Evaluation * CTCAE Grading * RECIST * Lugano Criteria * IMWG Criteria * IWCLL Criteria * ELN Criteria * Outcome Endpoint Analysis (ORR, DoR, PFS, OS, MRD) * Dose Escalation Assessment

Oncology Expert - Remote

Miami, FL · Remote

$150 - $200/hr

Clinical Trial Evaluation * CTCAE Grading * RECIST * Lugano Criteria * IMWG Criteria * IWCLL Criteria * ELN Criteria * Outcome Endpoint Analysis (ORR, DoR, PFS, OS, MRD) * Dose Escalation Assessment

Biostatistician

Clearwater, FL · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... endpoint expertise, and exposure to AI-assisted statistical review tools.

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... endpoint expertise, and exposure to AI-assisted statistical review tools.

Biostatistician

Tampa, FL · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... endpoint expertise, and exposure to AI-assisted statistical review tools.

next page

Showing results 1-20

Endpoint Clinical information

See Florida salary details

$10

$25

$67

How much do endpoint clinical jobs pay per hour?

As of Aug 24, 2026, the average hourly pay for endpoint clinical in Florida is $25.87, according to ZipRecruiter salary data. Most workers in this role earn between $12.40 and $24.62 per hour, depending on experience, location, and employer.

What is Endpoint Clinical?

Endpoint Clinical is a company that specializes in providing interactive response technology (IRT) solutions for clinical trials. They help pharmaceutical, biotech, and medical device companies manage patient randomization, drug supply logistics, and data collection more efficiently. Their platforms are designed to streamline clinical trial processes, ensure compliance, and improve data accuracy. Endpoint Clinical's services support global clinical trials, helping sponsors and sites manage complex protocols and improve outcomes.

What are the key skills and qualifications needed to thrive as an Endpoint Clinical professional?

To thrive as an Endpoint Clinical professional, you need a solid understanding of clinical trial processes, data management, and regulatory compliance, often supported by a degree in life sciences or related fields. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification are typically required. Strong attention to detail, organizational skills, and effective communication are valuable soft skills in this role. These abilities ensure accurate data handling, regulatory adherence, and smooth coordination across clinical research teams, which are critical for successful clinical trials.

How does working at Endpoint Clinical as a project manager involve collaboration with cross-functional teams?

At Endpoint Clinical, project managers regularly collaborate with cross-functional teams including clinical operations, data management, software development, and client services. This collaboration ensures that clinical trial systems are customized to client specifications and that timelines and regulatory requirements are met. Project managers often facilitate communication between internal teams and external stakeholders, coordinate project milestones, and address challenges proactively. This team-oriented structure helps deliver high-quality solutions and fosters professional development through exposure to different areas of the clinical trial process.

What is the difference between Endpoint Clinical vs Clinical Research Coordinator?

AspectEndpoint ClinicalClinical Research Coordinator
Required CredentialsBachelor's degree, clinical research experience, possibly certifications like CCRPBachelor's degree often required, certifications like CCRP or CCRC beneficial
Work EnvironmentPharmaceutical companies, clinical research organizations, hospitalsResearch sites, hospitals, clinics
Employer & Industry UsageUsed by CROs, pharma companies, biotech firmsCommonly employed at research sites and hospitals
Job FocusManaging clinical trial data, ensuring protocol compliance, supporting clinical operationsRecruiting participants, data collection, coordinating trial activities

Endpoint Clinical professionals typically work within pharmaceutical or CRO settings, focusing on clinical trial management and data oversight. Clinical Research Coordinators are more involved in participant recruitment and day-to-day trial operations at research sites. Both roles require similar credentials and are essential in the clinical research process, but they differ in scope and work environment.

Infographic showing various Endpoint Clinical job openings in Florida as of August 2026, with employment types broken down into 2% As Needed, 77% Full Time, 15% Part Time, and 6% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $53,807 per year, or $25.9 per hour.

Clinician (Oncology / Hematology) Expert - Remote

YO AI Labs

Miami, FL • Remote

$160 - $200/hr

Full-time

Posted 13 days ago


Job description

Job Title: Clinician (Oncology / Hematology)
Job Type: Contractor
Location: Remote

Job Overview

We are looking for experienced Oncology and Hematology Clinicians to support an innovative AI healthcare project. You will review clinical content, evaluate trial data, and provide expert medical insights to help improve AI systems. No prior AI experience is required.

Key Responsibilities
  • Review and evaluate oncology/hematology clinical documents and trial data.
  • Assess treatment outcomes, safety reports, adverse events, and dose escalation strategies.
  • Apply clinical response criteria such as RECIST, Lugano, IMWG, IWCLL, and ELN.
  • Provide clear, evidence-based clinical assessments and feedback.
  • Support AI model training through high-quality medical evaluations.
Required Skills
  • Clinical Oncology & Hematology
  • Clinical Trial Evaluation
  • CTCAE Grading
  • RECIST, Lugano, IMWG, IWCLL, ELN Criteria
  • Endpoint Analysis (ORR, DoR, PFS, OS, MRD)
  • Dose Escalation & Adverse Event Assessment
Preferred Qualifications
  • Board-certified Medical Oncologist and/or Hematologist.
  • 5+ years of post-training clinical experience.
  • Experience in clinical trials, medical monitoring, or clinical development.
  • Strong knowledge of oncology/hematology trial documentation and response criteria.
  • Excellent written communication skills.
  • Publications and AI-assisted clinical review experience are a plus