ZipRecruiter

Log In

1

Home Based Clinical Research Associate Jobs in Boca Raton, FL

Research Centers of America

Research Assistant I

Hollywood, FL · On-site

$17.50 - $24.25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

CenExel is a leading nationwide clinical research site and patient network serving the life ... Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments ...

Ambrosia Behavioral Health

Research Assistant

West Palm Beach, FL · On-site

$18.50 - $25.75/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... based therapies. Guided by our core values-- Compassion, Excellence, and Innovation --we provide ... Coordinate clinical research studies from startup through closeout. * Support participant ...

Research Centers of America

Research Assistant I

Hollywood, FL · On-site

$17.50 - $24.25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

CenExel is a leading nationwide clinical research site and patient network serving the life ... Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments ...

CenExel

Research Assistant I

Hollywood, FL · On-site

$17.50 - $24.25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

CenExel is a leading nationwide clinical research site and patient network serving the life ... Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments ...

Flourish Research

PATIENT RECRUITER

Boca Raton, FL · On-site

Maintaining and development of relationships with local ad sales associates and companies for advertising and enrolling patients for clinical research studies. Working with Clinical Research ...

Supreme Home Health Care LLC

Be Seen First

Home Health Clinical Supervisor (RN)

Hollywood, FL · On-site

$72K - $82K/yr

  • PTO

This is a hybrid position that combines field nursing supervision with office-based clinical ... Strong knowledge of Medicare and home health regulations

previous page

Showing results 41-60

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 Aug 20, 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 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 are the key skills and qualifications needed to thrive as a home based clinical research associate?

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 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 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 Trial Manager, Immunology

Syncromune

Fort Lauderdale, FL • On-site, Remote

$145K - $165K/yr

Full-time

Re-posted 15 hours ago

Job description

The Clinical Trial Manager (CTM) works closely with various internal team members and vendors as well as clinical sites to ensure that clinical trials are conducted in a timely fashion and in a manner compliant with SOPs, ICH/GCP/regulatory guidelines, company goals, and company timelines. This position is responsible for leading and managing the conduct of complex drug/device combination immuno-oncology clinical trials from study start-up to closeout. The CTM shall serve as the primary contact for clinical site personnel for trial activities and progress, including responding to issues and recommending corrective actions.
Responsibilities:
  • Participates in protocol, CRF and strategy development.
  • Prepares metrics and updates for management, as assigned.
  • Prepares and shares written and verbal reports on the status of clinical trials and significant issues impacting clinical trials.
  • Proactively identifies potential study issues/risks and recommends/implements solutions.
  • Participates in and facilitates CRO/vendor selection process for outsourced activities, as assigned.
  • Manages CRO interactions, including sponsor oversight of operational functional activities.
  • Prepares and/or reviews/approves study-related documents (Monitoring Plan, Communication Plan, Laboratory Manual, Procedures Manual, Pharmacy Manual, CRF Completion Guidelines, etc.).
  • Develop and maintain the Project Team List for assigned clinical trials.
  • Manages clinical monitoring activities ensuring compliance with Good Clinical Practice (GCP) and applicable regulations.
  • Participates in the development, review, and implementation of departmental SOPs and processes.
  • Recommends and implements innovative process ideas to impact clinical trials management.
  • Organizes and manages internal team meetings, investigator meetings, and other trial-specific meetings.
  • Serves as a liaison and resource for investigational sites of assigned studies.
  • Reviews site study documents (informed consent template, study tools/worksheets, etc.).
  • Participates in the training and evaluation of study personnel specific to assigned studies.
  • Performs some or all the duties and responsibilities outlined for Senior Clinical Research Associate, as needed.
  • Oversee and shepherd payments to sites through the payment approval process.
  • All other duties as assigned.

Requirements:
  • Bachelor's degree in life sciences, nursing, pharmacy, or a related field. Additional clinical trial certifications (e.g., ACRP, SOCRA) are a plus.
  • At least 5 years of experience in clinical research, clinical operations, (recent experience as a CRA in oncology; academic site level experience in oncology as a study coordinator is preferred).
  • Familiarity with clinical trial processes, Good Clinical Practice (GCP), and ICH guidelines.
  • Strong experience in oncology clinical trials.
  • Experience with phase I-II oncology studies from study start up through data lock.
  • Solid understanding of GCP, ICH guidelines, and regulatory requirements.
  • Strong scientific acumen and ability to grasp complex scientific and technical concepts.
  • Familiarity with 21CFR, ISO, ICH, GCP, and relevant regulations, standards, directives, and guidance is essential.
  • Excellent analytical and research skills, with a keen eye for detail.
  • Exceptional communication, organizational, and problem-solving skills.
  • Ability to work independently and collaboratively in a fast-paced, deadline-driven matrix environment.
  • Ability to set priorities and accomplish assigned work within deadlines.

Working Conditions:
  • Specify work environment:
  • The work environment shall be split between a virtual office environment and the Company headquarters in Fort Lauderdale, FL.
  • Domestic and International travel up to 30%.
  • Must have current passport or willingness to obtain immediately
  • Must be able to successfully pass a background check, drug testing, and other applicable vendor credentialing requirements
  • Ability to lift up to 35 pounds
  • Regularly required to stand, sit, talk, hear, and use hands
  • Prolonged periods of sitting and standing

Syncromune is an Equal Opportunity Employer.
The Company is required to provide a reasonable estimate of the salary range for this job in certain states and cities within the United States. Final determinations with respect to salary will take into account a number of factors, which may include, but not be limited to, the primary work location and the chosen candidate's relevant skills, experience, and education.
Expected US salary range: $145,000-165,000
This position generally is eligible for cash incentive compensation, equity incentive compensation, and employee benefits under the Company's benefit plans.
#remote

Apply