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Remote Clinical Trial Associate Jobs in Florida (NOW HIRING)

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 ... clinical trial data. This position involves reviewing scales administered by raters to confirm ...

YO AI Labs

Clinicia Expert - Remote

Miami, FL · Remote

$150 - $200/hr

Clinician Expert Remote Job Type: Contractor Location: Remote Job Overview We are seeking ... Analyze clinical study reports, safety reports, regulatory documents, and trial materials to assess ...

YO AI Labs

Biostatistician Expert - Remote

Miami, FL · Remote

$60 - $70/hr

Remote Job Type: Contractor Pay: $60-$65/hour Job Overview We are looking for an experienced ... Analyze and validate clinical trial data. * Review and interpret Statistical Analysis Plans (SAPs)

Danaher

Principal Clinical Scientist

Miami, FL · On-site +1

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 ...

YO AI Labs

Hematology Expert - Remote

Miami, FL · Remote

$150 - $200/hr

Hematology Expert Remote Job Type: Contractor Location: Remote Job Overview We are seeking ... Analyze clinical study reports, safety reports, regulatory documents, and trial materials to assess ...

YO AI Labs

Oncology Expert - Remote

Miami, FL · Remote

$150 - $200/hr

Oncology Expert Remote Job Type: Contractor Location: Remote Job Overview We are seeking ... Analyze clinical study reports, safety reports, regulatory documents, and trial materials to assess ...

Danaher

Principal Clinical Scientist

Miami, FL · On-site +1

The Principal Clinical Scientist responsible for clinical trial strategies within the US and EU ... Hematology and Urinalysis business unit located in Miami, FK and will be fully remote In this role ...

Careerxchange

Oncology CTMS Analyst

Miami, FL · Remote

$28 - $38/hr

This fully remote opportunity is ideal for an experienced Clinical Trials Management System (CTMS ... trial data management. If you have hands-on CTMS experience in a hospital or academic research ...

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Remote Clinical Trial Associate information

What does a remote clinical trial associate do?

A Remote Clinical Trial Associate (CTA) supports the planning, execution, and management of clinical trials from a remote location. Their responsibilities include handling documentation, assisting with regulatory submissions, maintaining trial records, and coordinating communication between trial sites, sponsors, and regulatory bodies. Remote CTAs play a crucial role in ensuring that trials are conducted according to protocols, timelines, and regulatory requirements, all while working offsite. This allows for greater flexibility and can improve efficiency in clinical research processes.

What are the key skills and qualifications needed to thrive as a remote clinical trial associate, and why are they important?

To thrive as a Remote Clinical Trial Associate, you need a solid understanding of clinical research processes, regulatory guidelines, and typically a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and Good Clinical Practice (GCP) certification are commonly required. Strong organizational skills, attention to detail, and effective communication are crucial soft skills for managing study documentation and collaborating with remote teams. These competencies ensure trials are conducted efficiently, compliantly, and with high data integrity in a virtual environment.

What are some common challenges faced by remote clinical trial associates, and how can they be managed?

Remote Clinical Trial Associates often encounter challenges such as maintaining consistent communication with on-site teams, managing multiple studies across different time zones, and ensuring accurate documentation while working virtually. These can be managed by leveraging robust digital communication tools, setting clear expectations for updates, and staying organized with project management software. Proactively building relationships with colleagues and participating in regular virtual meetings also helps ensure alignment and smooth coordination throughout the trial process.

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

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

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

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

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

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

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

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

Remote Clinical Trial Associate jobs near you
Infographic showing various Remote Clinical Trial Associate job openings in Florida as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 22% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution.

Clinical Trial Manager, Immunology

SAb Biotherapeutics, Inc

Miami Beach, FL • On-site, Remote

$150K - $165K/yr

Full-time

Re-posted 22 days ago

Key responsibilities

  • Oversee the planning, implementation, and management of clinical trials to ensure compliance with regulatory guidelines and quality standards.

  • Manage all aspects of clinical trial operations, including site selection, vendor oversight, budget tracking, and ensuring adherence to timelines.

  • Collaborate with cross-functional teams and maintain relationships with clinical trial sites to support trial execution and compliance.

Job description

The Clinical Trial Manager (CTM) oversees the planning, implementation and management of clinical trials to ensure they are conducted efficiently, ethically, and in compliance with regulatory guidelines. The CTM plays a critical role in coordinating cross functional teams, maintaining budgets, timelines, and quality standards, and ensuring the successful execution of clinical studies.
Duties and Responsibilities (Responsibilities include but are not limited to):
Study Planning and Execution:
  • Lead the design and implementation of clinical trial protocols, including site selection, patient recruitment strategies, and timeline development.
  • Contributing to the development of study protocols, protocol amendments, study manuals, Informed Consent Forms (ICFs), Case Report Forms (CRFs), Investigator Brochures (IBs) and other study-related documents as require
  • Oversee implementation and maintenance of Trial Master File for inspection readiness
Project Management:
  • Manage all aspects of clinical trial operations, ensuring adherence to timelines, budgets, and regulatory requirements.
  • Participate in the identification, evaluation, selection, and oversight of clinical trial sites in collaboration with the Clinical Research Organization (CRO)
  • Manage external vendors with oversight of activities
  • Review invoices and track study budget according to the forecast, working closely with finance and clinical business operations
Team Leadership:
  • Collaborate with cross-functional teams including clinical research associates, data managers, and regulatory affairs to ensure successful trial execution.
Site Management:
  • Establish and maintain strong relationships with clinical trial sites. Provide ongoing support and oversight to ensure compliance with protocol and regulatory standards.
Data Integrity and Compliance:
  • Monitor trial progress, ensuring accurate data collection, timely reporting, and adherence to Good Clinical Practice (GCP) guidelines.
Risk Management:
  • Identify potential study risks and develop mitigation strategies to ensure successful trial outcomes.
Communication:
  • Prepare and present updates to stakeholders, including internal teams and external partners. Facilitate regular meetings to discuss study progress and address challenges.
Requirements:
  • B.S. degree with minimum 6-8+ years of experience managing clinical trials in biotech, pharmaceutical
  • Strong clinical study conduct experience from start-up through close-out, with global trial and CRO management experience
  • Experience with phase II, III study oversight and management
  • Experience with timeline management
  • Strong leadership, effective decision making, and problem-solving skills required
  • Document reviews in relevant systems with a focus on inspection readiness
  • Working knowledge of relevant GCPs and FDA, EMA and MHRA regulations
  • Demonstrated experience using various EDC, CTMS and eTMF (Veeva, Agatha) systems. Experience with operational financial tracking systems a plus
  • Demonstrated proficiency using MS Office applications, including MS Word, Excel, PowerPoint
  • Experience using Smartsheet
  • Ability to work effectively with minimal supervision and multi-task activities to effectively manage deliverables across all trials
  • Excellent written and verbal communication skills
Working Environment and Travel:
Generally accepted office working conditions
Travel up to 25% - ability to travel domestically and internationally
Prefer candidates located in Central or Eastern Time Zones
Physical Requirements:
While performing the duties of this job, the employee is regularly required to walk, stand and sit. The employee will be able to use a computer for extended periods at any given time. The employee must regularly lift and/or move up to 10 pounds.
ADA:
The employer will make reasonable accommodations in compliance with the Americans with Disabilities Act of 1990.
SAB Bio is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. SAB Bio is committed to the principle of equal employment opportunity for all employees and does not discriminate based on race, religion, color, sex, gender identify, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other legally protected status. EOE/AA/Vets
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