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Home Based Clinical Research Associate Jobs in Boca Raton, FL

Flourish Research

Clinical Research Coordinator

Boca Raton, FL · On-site

$23 - $30.50/hr

About Us Flourish Research is where clinical trials thrive. Flourish Research is one of the ... Employment decisions are based on merit and business needs, and not on race, color, sex, (including ...

Flourish Research

Clinical Research Coordinator

Boca Raton, FL · On-site

$23 - $30.50/hr

About Us Flourish Research is where clinical trials thrive. Flourish Research is one of the ... Employment decisions are based on merit and business needs, and not on race, color, sex, (including ...

Flourish Research

Clinical Research Coordinator

Boca Raton, FL · On-site

$23 - $30.50/hr

About Us Flourish Research is where clinical trials thrive. Flourish Research is one of the ... Employment decisions are based on merit and business needs, and not on race, color, sex, (including ...

Flourish Research

Clinical Research Coordinator

Boca Raton, FL · On-site

$23 - $30.50/hr

About Us Flourish Research is where clinical trials thrive. Flourish Research is one of the ... Employment decisions are based on merit and business needs, and not on race, color, sex, (including ...

Flourish Research

Clinical Research Coordinator

Boca Raton, FL · On-site

$23 - $30.50/hr

About Us Flourish Research is where clinical trials thrive. Flourish Research is one of the ... Employment decisions are based on merit and business needs, and not on race, color, sex, (including ...

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All JobsHome Based Clinical Research Associate JobsHome Based Clinical Research Associate Jobs in Boca Raton, FL

Home Based Clinical Research Associate information

See Boca Raton, FL salary details

$11

$39

$66

How much do home based clinical research associate jobs pay per hour?

As of Jul 27, 2026, the average hourly pay for home based clinical research associate in Boca Raton, FL is $39.03, according to ZipRecruiter salary data. Most workers in this role earn between $27.36 and $49.95 per hour, depending on experience, location, and employer.

What are some common challenges faced by Home Based Clinical Research Associates and how can they be managed?

Home Based Clinical Research Associates (CRAs) often face challenges such as maintaining effective communication with site staff and sponsors, managing time efficiently, and staying organized while working remotely. To manage these, CRAs typically rely on regular virtual meetings, robust project management tools, and clear documentation practices. Building strong relationships with site teams and proactively addressing issues also helps ensure smooth study progress and data integrity. Adapting to evolving technologies and maintaining self-discipline are key for success in this remote role.

What are the key skills and qualifications needed to thrive as a Home Based Clinical Research Associate, and why are they important?

To thrive as a Home Based Clinical Research Associate, you need a solid understanding of clinical trial protocols, regulatory requirements (like GCP), and a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, remote monitoring tools, and relevant certifications such as ACRP or SOCRA are typically required. Excellent organizational skills, attention to detail, and strong verbal and written communication are vital for effective remote collaboration and documentation. These skills ensure clinical trials are conducted efficiently, ethically, and in compliance with regulatory standards, even when working remotely.

What is a Home Based Clinical Research Associate?

A Home Based Clinical Research Associate (CRA) is a professional responsible for monitoring clinical trials and ensuring they comply with regulatory requirements, scientific protocols, and Good Clinical Practice guidelines, all while working remotely from home. They communicate with medical sites, review study documentation, and help maintain data integrity and patient safety. This role requires strong organizational and communication skills, as well as the ability to manage multiple tasks independently from a remote setting.

What is the difference between Home Based Clinical Research Associate vs On-Site Clinical Research Associate?

AspectHome Based Clinical Research AssociateOn-Site Clinical Research Associate
Work EnvironmentPrimarily remote, working from home and visiting sites as neededOn-site at clinical trial locations or sites
Required CredentialsTypically requires a clinical research certification, degree in health sciences, and relevant experienceSimilar credentials, often requiring clinical research certification and healthcare background
Employer & Industry UsageUsed by pharmaceutical companies, CROs, and biotech firms for remote monitoring rolesCommon in hospitals, research centers, and on-site clinical trial sites

The main difference between a Home Based Clinical Research Associate and an On-Site Clinical Research Associate lies in their work environment. The home-based role allows remote monitoring and site visits, offering flexibility, while the on-site role involves working directly at clinical trial locations. Both roles require similar credentials and are integral to clinical research, but their daily operations and work settings differ significantly.

What are popular job titles related to Home Based Clinical Research Associate jobs in Boca Raton, FL? For Home Based Clinical Research Associate jobs in Boca Raton, FL, the most frequently searched job titles are:
What job categories do people searching Home Based Clinical Research Associate jobs in Boca Raton, FL look for? The top searched job categories for Home Based Clinical Research Associate jobs in Boca Raton, FL are:
What cities near Boca Raton, FL are hiring for Home Based Clinical Research Associate jobs? Cities near Boca Raton, FL with the most Home Based Clinical Research Associate job openings:
Home Based Clinical Research Associate jobs near you
Clinical Research Associate II

Clinical Research Associate II

Icon plc

Fort Lauderdale, FL

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 16 days ago

Job description

Clinical Research Associate - Oncology - West Palm Beach, FL

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


What You Will Be Doing:

  • Serve as the primary point of contact between investigational sites and the sponsor

  • Conduct all types of site visits, including selection, initiation, routine monitoring, and close-out

  • Ensure site compliance with ICH-GCP, SOPs, and regulations

  • Maintain up-to-date documentation in CTMS and eTMF systems

  • Support and track site staff training and maintain compliance records

  • Monitor patient safety, ensuring timely and accurate AE/SAE/PQC reporting

  • Support subject recruitment and retention efforts at the site level

  • Oversee drug accountability and ensure proper storage, return, or destruction

  • Resolve data queries and drive timely, high-quality data entry

  • Document site progress and escalate risks or issues to the clinical team

  • Assist in tracking site budgets and ensuring timely site payments (as applicable)

  • Collaborate with cross-functional partners including CTAs, LTMs, and CTMs

You are:

  • A graduate with a Bachelor's degree in Life Sciences or equivalent, or a qualified RN

  • Eligible to work in United States without visa sponsorship

  • A clinical research professional with 2+ years of on-site monitoring experience in the pharmaceutical or CRO industry

  • Experienced monitoring Oncology (I.e. Prostate Cancer, and Lung Cancer) and/or Hematology Oncology clinical studies

  • Proficient in ICH-GCP, local regulatory requirements, and clinical systems like CTMS and eTMF

  • A clear communicator, problem-solver, and collaborative team player

  • Willing and able to travel up to 50% for on-site monitoring visits across southeast region; preference given to candidates residing in West Palm Beach, FL near major HUB airports to support efficient regional travel


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a requesthere.

Are you a current ICON Employee? Please click here to apply

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