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Esource Jobs in Florida (NOW HIRING)

Gastromed, LLC

Sub-Investigator (Nurse Practitioner)

Miami, FL · On-site

$98K - $133.90K/yr

Maintain accurate, timely, and complete documentation in the eSource systems MINIMUM QUALIFICATIONS * Licensed Nurse Practitioner in the state of Florida (active and in good standing) * Minimum 1-2 ...

Denali Health

Research Assistant

Plant City, FL · On-site

$16.75 - $23.25/hr

Document carefully: transcribe notes to source/eSource, upload/scans to the eISF, and enter data in eCRFs as delegated, following ICH-GCP/HIPAA. * Tackle data quality tasks: pre-fill templates, check ...

ObjectiveHealth

Clinical Research Coordinator I

Ocala, FL · On-site

$22.50 - $30/hr

You have the ability to stay focused while running different protocols, resolving and submitting IRB responses and audit findings, tracking AE and SAE events, and maintaining eSource material for ...

ObjectiveHealth

Clinical Research Coordinator I

Ocala, FL · On-site

$22.50 - $30/hr

You have the ability to stay focused while running different protocols, resolving and submitting IRB responses and audit findings, tracking AE and SAE events, and maintaining eSource material for ...

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How much do esource jobs pay per hour?

As of May 28, 2026, the average hourly pay for esource in Florida is $20.98, according to ZipRecruiter salary data. Most workers in this role earn between $12.06 and $24.51 per hour, depending on experience, location, and employer.

What is an Esource job?

An Esource job typically involves managing electronic source data in clinical research or healthcare settings. Professionals in this role ensure the accurate collection, storage, and integration of digital records, often replacing traditional paper documentation. They may work with electronic data capture (EDC) systems, regulatory compliance, and data quality control. Strong attention to detail and familiarity with clinical or regulatory environments are essential.

What are the key skills and qualifications needed to thrive in the Esource position, and why are they important?

To succeed as an Esource Specialist, you need a background in clinical research, an understanding of data management, and familiarity with regulatory guidelines, often supported by a degree in life sciences or a related field. Expertise in electronic data capture (EDC) systems, eSource platforms such as Medidata Rave or OpenClinica, and possibly certifications in clinical data management are highly valued. Attention to detail, problem-solving ability, and strong collaboration skills are essential for working with research teams and ensuring data integrity. These competencies are vital to ensure accurate, compliant, and efficient collection and management of clinical trial data.

What are the main responsibilities of an Esource Specialist in a clinical research setting?

As an Esource Specialist, your primary responsibilities include implementing and maintaining electronic source data systems for clinical studies, ensuring data accuracy, and supporting compliance with regulatory standards. You will often work closely with clinical research coordinators, data managers, and IT teams to set up, test, and troubleshoot eSource platforms. Additionally, you may assist in training site staff, creating documentation, and participating in data quality audits. This role is a key part of the clinical research process, helping streamline workflows and contribute to the reliability of study outcomes.
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Esource jobs near you
Infographic showing various Esource job openings in Florida as of May 2026, with employment types broken down into 90% Full Time, and 10% Contract. Highlights an 77% In-person, and 23% Remote job distribution, with an average salary of $43,646 per year, or $21 per hour.

Sub-Investigator (Nurse Practitioner)

Gastromed, LLC

Miami, FL • On-site

$98K - $133.90K/yr

Full-time

Posted 21 days ago

Job description

JOB TITLE: Sub-Investigator (Nurse Practitioner)

REPORTS TO: Physicians/Investigators and Vice President

FLSA STATUS: Exempt

ABOUT US

We are a high-performing, multispecialty clinical research site with a strong focus in gastroenterology and dermatology. In partnership with leading physician groups, we provide patients access to cutting-edge clinical trials while maintaining the highest standards of data quality, patient care, and regulatory compliance. Our site is recognized for rapid enrollment, strong retention, and operational excellence across both interventional and observational studies.

POSITION OVERVIEW

We are seeking a motivated and detail-oriented Nurse Practitioner (NP) to serve as a Sub-Investigator supporting clinical trials across multiple therapeutic areas. This role is ideal for a provider interested in combining patient care with research, working alongside experienced Principal Investigators and clinical research teams.


The Sub-Investigator will play a key role in subject safety, protocol adherence, and high-quality data generation while helping to drive study success and patient engagement.


KEY RESPONSIBILITIES

  • Perform study-related clinical assessments, including medical history, physical exams, and eligibility evaluations
  • Serve as a Sub-Investigator on assigned protocols, ensuring compliance with protocol, GCP, and regulatory requirements
  • Assess and document adverse events, concomitant medications, and subject safety throughout study participation
  • Support informed consent discussions and ensure patient understanding of study participation
  • Collaborate with study coordinators, investigators, and sponsors to ensure protocol adherence and data accuracy
  • Review and sign off on study-related source documentation as delegated
  • Participate in monitoring visits, audits, and sponsor interactions as needed
  • Assist in recruitment efforts and patient identification in collaboration with the clinical team
  • Maintain accurate, timely, and complete documentation in the eSource systems



MINIMUM QUALIFICATIONS

  • Licensed Nurse Practitioner in the state of Florida (active and in good standing)
  • Minimum 1–2 years of clinical experience required; clinical research experience preferred
  • Strong understanding of clinical documentation and patient care standards
  • Knowledge of Good Clinical Practice (GCP) guidelines preferred
  • Excellent communication, organization, and attention to details
  • Ability to work in a fast-paced, team-oriented environment



PREFERRED EXPERIENCE

  • Experience in gastroenterology, dermatology, or internal medicine
  • Prior experience as a Sub-Investigator or in a clinical research setting
  • Familiarity with eSource systems (e.g., CRIO)


WHY JOIN OUR TEAM?

  • Opportunity to work at a high-enrolling, industry-leading research site
  • Exposure to cutting-edge therapies and innovative clinical trials
  • Collaborative, fast-paced, and growth-oriented environment
  • Competitive compensation based on experience
  • Opportunity for professional development within clinical research