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Remote Clinical Trials Jobs in Florida (NOW HIRING)

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 ...

Clinicia Expert - Remote

Miami, FL · Remote

$150 - $200/hr

Clinician Expert Remote Job Type: Contractor Location: Remote Job Overview We are seeking ... Direct experience with clinical trials as an investigator, sub-investigator, medical monitor ...

Remote Job Type: Contractor Pay: $60-$65/hour Job Overview We are looking for an experienced ... in clinical trials (Sponsor, CRO, or Academic Research). * MSc or PhD in Biostatistics, Statistics ...

Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... Experience in CNS trials preferred. * Skills: * Strong interpersonal and communication skills for ...

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Remote Clinical Trials information

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$46

$71

How much do remote clinical trials jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for remote clinical trials in Florida is $46.72, according to ZipRecruiter salary data. Most workers in this role earn between $37.88 and $52.64 per hour, depending on experience, location, and employer.

What is a remote clinical trial?

A Remote Clinical Trials job involves managing or supporting clinical research studies from a remote location rather than on-site at a study facility. Professionals in these roles may recruit participants, monitor data, ensure regulatory compliance, and coordinate with research teams using digital tools. Common positions include clinical research associates, coordinators, and data managers. Advances in telemedicine and digital health technology have made remote clinical trials more feasible, improving accessibility for patients and researchers.

What are the key skills and qualifications needed to thrive in remote clinical trials?

To excel in Remote Clinical Trials roles, candidates should possess a background in clinical research, data management, regulatory compliance, and often a related degree such as life sciences or nursing. Proficiency with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications like GCP (Good Clinical Practice) are highly valued. Strong organizational skills, attention to detail, and clear virtual communication are vital soft skills for coordinating remote trial activities. These skills ensure accurate data collection, regulatory adherence, and effective team collaboration in a remote environment.

What are some common challenges faced in remote clinical trials roles, and how are they typically addressed?

Remote clinical trials professionals often face challenges like coordinating across different time zones, ensuring data accuracy without on-site supervision, and maintaining clear communication among dispersed teams. These challenges are typically addressed by leveraging robust digital platforms for data entry and communication, setting clear protocols for remote monitoring, and holding regular virtual meetings to maintain team alignment. Successful remote trial specialists are proactive in problem-solving and prioritize transparent communication with both participants and colleagues. This approach helps maintain trial integrity and data quality while facilitating collaboration despite the physical distance.

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

The most popular types of Clinical Trials jobs in Florida are:

What cities in Florida are hiring for Remote Clinical Trials jobs?

Cities in Florida with the most Remote Clinical Trials job openings:

Infographic showing various Remote Clinical Trials job openings in Florida as of August 2026, with employment types broken down into 74% Full Time, and 26% Contract. Highlights an 100% Remote job distribution, with an average salary of $97,174 per year, or $46.7 per hour.

Senior Clinical Trial Liaison (US)

Worldwide Clinical Trials

Miami, FL • On-site, Remote

Full-time

Posted 3 days ago

New


Job description

Who we are
We're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.
Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.
Why Worldwide
We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us!
What the Sr. Clinical Trial Liaison does at Worldwide
The Sr. Clinical Trial Liaison will serve in part as a Strategic Site Relationship Manager, establishing and maintaining strong relationships with clinical investigators and site staff within their therapeutic areas of expertise and providing insights to internal teams and sponsors, with an overall focus on successful trial execution. The Clinical Trial Liaison will also assist with the overall remit for Scientific Solutions, ensuring quality endpoints are achieved through optimal site selection and assisting sites with understanding of protocols and enrolment of proper trial participants.
What you will do
  • Establish and maintain relationships with key opinion leaders, sites, and their staff.
  • Conduct targeted conversations with the investigators and site staff regarding operational challenges, including but not limited to those related to patient recruitment and retention.
  • Have clinical and scientific discussions with investigators to ensure overall quality of study endpoints, including but not limited to understanding of clinical protocols, study feasibility, and enrolment and retention of appropriate trial participants.
  • Convey KOL and site staff feedback and insight to internal and external teams.
  • Support and guide project teams with site identification and selection based on knowledge of site capabilities and anticipated protocol challenges.
  • Support project teams regarding site performance issues. Work closely with internal study teams and sites to foresee and proactively manage study site issues as they occur to maintain study timelines and quality. Initiate, recommend and communicate corrective actions as needed.

What you will bring to the role
  • Excellent networking skills to represent Worldwide with key local stakeholders.
  • Excellent written and verbal communication skills - able to interact with physicians and all levels of internal and external management.
  • Excellent negotiation, influencing and problem-solving skills.
  • Self-motivated with proactive issue monitoring and management including risk assessment and contingency planning.
  • Possess a combination of critical thinking and operational expertise and efficiency.
  • Work independently.

Your experience
  • A doctoral degree is required, or alternatively, a candidate may possess a bachelor's/master's degree accompanied by experience as an advanced practice provider, such as a Physician's Assistant, Nurse Practitioner, or another licensed healthcare provider.
  • Minimum of 7 years' experience in clinical research in academia, Pharma, Biotech or CRO, including background in operational aspects of clinical research; at least 3 years as CTL or Medical Science Liaison preferred
  • Minimum of 3 years' experience in the therapeutic area/indication assigned.
  • Demonstrated experience of working directly with clinical sites and investigators.
  • Demonstrated customer service and relationship building skills with clinical sites (on site and remote).

At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace by providing transparent compensation.
The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates):
United States of America - $134,500.00 - $267,500.00
The salary range provided is intended to give candidates an understanding of potential earnings. Compensation will fall within the provided range, and it not a guarantee of exact salary. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location. We ensure pay equity and transparency and comply with all applicable labor laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage.
We love knowing that someone is going to have a better life because of the work we do.
To view our other roles, check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.