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Remote Senior Clinical Research Associate Jobs in Boca Raton, FL

ICON

Clinical Research Associate II

West Palm Beach, FL · On-site +1

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 ...

EVENING POST GROUP

VA ASSOCIATE ADVOCATE

Plantation, FL · Remote

$62K - $104K/yr

The VA Associate Advocate will assist the Senior Advocate/Team Leader of an advocate department and ... This is a remote work from home position. Our benefits package includes health, dental, and vision ...

Advocacy Solutions

VA ASSOCIATE ADVOCATE

Plantation, FL · On-site +1

$62K - $104K/yr

The VA Associate Advocate will assist the Senior Advocate/Team Leader of an advocate department and ... This is a remote work from home position. Our benefits package includes health, dental, and vision ...

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All JobsClinical Research Associate JobsRemote Senior Clinical Research Associate JobsRemote Senior Clinical Research Associate Jobs in Boca Raton, FL

Remote Senior Clinical Research Associate information

See Boca Raton, FL salary details

$34.2K

$89.5K

$136.2K

How much do remote senior clinical research associate jobs pay per year?

As of Jul 25, 2026, the average yearly pay for remote senior clinical research associate in Boca Raton, FL is $89,501.00, according to ZipRecruiter salary data. Most workers in this role earn between $59,300.00 and $121,500.00 per year, depending on experience, location, and employer.

What is a Remote Senior Clinical Research Associate?

A Remote Senior Clinical Research Associate (CRA) is a highly experienced professional who oversees and monitors clinical trials, ensuring they are conducted according to regulatory guidelines, protocols, and good clinical practice (GCP) standards, all while working remotely. Senior CRAs are responsible for site management, data verification, and ensuring participant safety and data integrity. They typically act as the main point of contact between the sponsor and the clinical trial sites, and may also mentor or train junior staff. Working remotely allows them to manage multiple sites across different locations more efficiently. This role requires strong communication, organizational, and analytical skills, as well as extensive clinical research experience.

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

To thrive as a Remote Senior Clinical Research Associate, you need expertise in clinical trial management, regulatory compliance, and a background in life sciences, often supported by a bachelor's degree and several years of CRA experience. Familiarity with electronic data capture (EDC) systems, ICH-GCP guidelines, and certifications like ACRP or SOCRA are commonly required. Strong organizational skills, attention to detail, and excellent communication are crucial for managing trials remotely and ensuring protocol adherence. These skills are vital to maintaining data integrity, regulatory compliance, and successful study outcomes across geographically dispersed sites.

What is the difference between Remote Senior Clinical Research Associate vs Remote Clinical Research Associate?

AspectRemote Senior Clinical Research AssociateRemote Clinical Research Associate
Required CredentialsBachelor's degree, clinical research experience, often some certificationBachelor's degree, entry-level experience, often similar certifications
Work EnvironmentRemote, overseeing multiple sites, higher responsibilityRemote, supporting clinical trials, more focused on data collection
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsSimilar employers, often entry-level or supporting roles
Search & Comparison IntentUnderstanding senior roles, career progressionEntry-level understanding, role clarification

The Remote Senior Clinical Research Associate typically has more experience, greater responsibilities, and oversees multiple sites remotely. The Remote Clinical Research Associate is often an entry-level or supporting role focused on data collection and site support. Both roles are essential in clinical trials, but the senior position involves higher oversight and decision-making.

What are some common challenges faced by Remote Senior Clinical Research Associates, and how can they be managed?

Remote Senior Clinical Research Associates often face challenges related to maintaining effective communication with site staff and sponsors, as well as ensuring protocol compliance without frequent on-site visits. To manage these, it's important to leverage digital monitoring tools, schedule regular virtual check-ins, and develop strong organizational habits for tracking site progress. Building trusting relationships with site teams and being proactive in addressing issues can also help ensure studies stay on track, even when working remotely.
What are popular job titles related to Remote Senior Clinical Research Associate jobs in Boca Raton, FL? For Remote Senior Clinical Research Associate jobs in Boca Raton, FL, the most frequently searched job titles are:
What job categories do people searching Remote Senior Clinical Research Associate jobs in Boca Raton, FL look for? The top searched job categories for Remote Senior Clinical Research Associate jobs in Boca Raton, FL are:
What cities near Boca Raton, FL are hiring for Remote Senior Clinical Research Associate jobs? Cities near Boca Raton, FL with the most Remote Senior Clinical Research Associate job openings:
Remote Senior Clinical Research Associate jobs near you
Clinical Trial Manager, Immunology

Clinical Trial Manager, Immunology

Syncromune

Fort Lauderdale, FL • On-site, Remote

$145K - $165K/yr

Full-time

Posted 5 days 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.
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