ZipRecruiter

Log In

1

Clinical Trial Transparency Associate Jobs in Florida

Danaher

Principal Clinical Scientist

Miami, FL · On-site +1

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Our associates are involved in every stage of diagnostics, from ideation to development and ... This role is responsible for clinical trial strategies within the US and EU regions for Danaher ...

UF Health

Research Associate - Urology

Jacksonville, FL · On-site

Adheres to ongoing clinical trial protocol-specific procedures as well as good clinical practice ... High School Diploma required Associates preferred Additional Duties: Additional duties as assigned ...

System One

Clinical Research Coordinator

New Port Richey, FL · On-site

$26 - $30/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

High school diploma or equivalent required; an associate's degree or higher in a health-related ... Proficiency with electronic data capture systems, clinical trial management software, and Microsoft ...

previous pagenext page

Showing results 21-40

All JobsClinical Trial Transparency Associate JobsClinical Trial Transparency Associate Jobs in Florida

Clinical Trial Transparency Associate information

See Florida salary details

$12

$29

$52

How much do clinical trial transparency associate jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for clinical trial transparency associate in Florida is $29.88, according to ZipRecruiter salary data. Most workers in this role earn between $24.09 and $32.88 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a clinical trial transparency associate?

To thrive as a Clinical Trial Transparency Associate, you need a solid understanding of clinical research processes, regulatory requirements (such as FDA, EMA, and ICMJE), and a relevant life sciences degree. Familiarity with clinical trial registries (e.g., ClinicalTrials.gov), disclosure platforms, and data anonymization tools is typically required. Exceptional attention to detail, organizational skills, and the ability to communicate complex information clearly are vital soft skills. These competencies ensure accurate and compliant disclosure of clinical trial data, supporting regulatory obligations and public trust in research.

What is a clinical trial transparency associate?

Clinical Trial Transparency Associates are professionals responsible for ensuring that information about clinical trials is accurately disclosed and publicly available in compliance with regulatory requirements. Their work includes preparing and submitting trial data to clinical trial registries, redacting sensitive information, and supporting the publication of trial results. They help organizations maintain transparency with stakeholders, including patients, regulators, and the scientific community. This role is essential to promote trust, ethical standards, and data sharing in medical research.

What is the difference between Clinical Trial Transparency Associate vs Clinical Data Coordinator?

AspectClinical Trial Transparency AssociateClinical Data Coordinator
Required CredentialsBachelor's degree, knowledge of clinical trial regulationsBachelor's degree, understanding of clinical data management
Work EnvironmentPharmaceutical or biotech companies, CROsResearch sites, hospitals, clinical research organizations
Employer & Industry UsageUsed in clinical trial disclosure and transparency effortsUsed in managing and coordinating clinical data collection
Common Search & Comparison IntentUnderstanding roles in clinical trial transparencyDistinguishing data management roles in clinical research

The Clinical Trial Transparency Associate focuses on ensuring clinical trial data is publicly disclosed in compliance with regulations, while the Clinical Data Coordinator manages and organizes clinical data collection and entry. Both roles require a background in clinical research but serve different functions within the clinical trial process.

What are some typical challenges faced by a clinical trial transparency associate when managing trial disclosure requirements?

Clinical Trial Transparency Associates often encounter challenges in navigating diverse regulatory requirements across different countries, as disclosure rules can vary significantly by region and sponsor. Coordinating with multiple stakeholders—from clinical teams to legal and regulatory departments—can also be complex, especially when ensuring timely and accurate data submissions. Staying updated on evolving transparency guidelines and managing large volumes of documentation are key aspects of the role. Proactive communication, strong organizational skills, and attention to detail are essential to successfully overcoming these challenges.

What are the most commonly searched types of Clinical Trial Transparency jobs in Florida?

The most popular types of Clinical Trial Transparency jobs in Florida are:

What are popular job titles related to Clinical Trial Transparency Associate jobs in Florida?

For Clinical Trial Transparency Associate jobs in Florida, the most frequently searched job titles are:

What job categories do people searching Clinical Trial Transparency Associate jobs in Florida look for?

The top searched job categories for Clinical Trial Transparency Associate jobs in Florida are:

What cities in Florida are hiring for Clinical Trial Transparency Associate jobs?

Cities in Florida with the most Clinical Trial Transparency Associate job openings:

Clinical Trial Transparency Associate jobs near you

RN or LPN Clinical Research Coordinator

Cardiovascular Associates of America

Palm Beach Gardens, FL • On-site

$65K - $81K/yr

Full-time

Re-posted 5 days ago

Job description

Job Title: Clinical Research Coordinator
Location: Palm Beach Gardens, FL
This is not a remote position. This is an in-person position in Palm Beach Gardens, Florida
Job Type: Full-time
About CVAUSA:
Cardiovascular Associates of America (CVAUSA) is a rapidly growing leader in cardiovascular care, committed to advancing medical research and improving patient outcomes. As part of our expansion, we are increasing our clinical trial operations and are seeking dynamic, results-driven professionals to join our team in Palm Beach Gardens, Florida.
At CVAUSA, we are focused on innovation and excellence in cardiovascular research, and we believe the best results come from individuals who are passionate about making a difference.
We are hiring a Clinical Research Coordinator for our Palm Beach Gardens office. The Research Coordinator will be responsible for leading the growth and development of the research program while also collaborating with clinic staff on existing and new clinical trials. As part of CVAUSA's national network, this role offers the opportunity to collaborate with teams across the country and make an impact both locally and nationwide.
Position Overview:
As a Clinical Research Coordinator, you will play a key role in managing and overseeing all aspects of clinical trials and site operations. You will have the opportunity to take ownership of your projects, driving them forward with innovation, efficiency, and excellence. This is an excellent opportunity for an ambitious, goal-oriented individual who thrives in an independent, fast-paced environment.
Key Responsibilities:
  • Clinical Trial Management: Oversee all aspects of clinical trials, including patient recruitment, screening, and enrollment. Ensure protocols are followed meticulously.
  • Site Operations: Manage day-to-day site operations, ensuring all activities comply with regulatory requirements and study protocols.
  • Data Management: Collect, verify, and manage clinical trial data, ensuring accuracy and completeness.
  • Communication & Reporting: Serve as the primary point of contact for study sponsors, participants, and stakeholders. Provide regular updates and progress reports.
  • Regulatory Compliance: Maintain up-to-date documentation, including regulatory submissions and patient records, in compliance with ethical and legal standards.
  • Problem Solving & Innovation: Identify opportunities for process improvement and implement solutions to enhance efficiency and trial performance.

What We're Looking For:
  • Goal-Driven & Independent: Thrives in an autonomous environment and takes ownership of responsibilities.
  • Innovative & Results-Oriented: Eager to contribute to growth and bring effective solutions.
  • Detail-Oriented & Organized: Able to manage multiple priorities while maintaining high quality.
  • Strong Communicator: Effectively communicates with sponsors, site staff, and participants.

Experience & Qualifications:
  • Clinical experience in cardiovascular medicine in a licensed role (e.g., RN, technologist, medical assistant, etc.)
  • Bachelor's degree in a relevant field (life sciences, healthcare, or clinical research)
  • Experience managing clinical trials, leading enrollment, and developing research programs
  • Strong organizational and time management skills
  • Clinical research certification (e.g., CCRP) preferred
  • Knowledge of GCP, ICH guidelines, and regulatory requirements

Why CVAUSA?
At CVAUSA, we believe in the power of innovation and are looking for professionals eager to make an impact in cardiovascular research. As part of our growing organization, you'll be at the forefront of cutting-edge clinical trials.
You will make meaningful contributions to improving cardiovascular care while leading the growth of research at our Palm Beach Gardens site, with opportunities to collaborate across our national network. We offer competitive compensation, flexible working hours, and a supportive, dynamic environment where your contributions are valued.

Apply