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Weekend Clinical Trial Rn Jobs in Florida (NOW HIRING)

Sitero LLC

Lead Clinical Trial Associate

Coral Gables, FL · On-site

$70K - $80K/yr

Lead Clinical Trial Associate Location: 3 days per week in our Coral Gables, Florida office. 2 days ... Bachelor's or Master's degree in Life Sciences, Nursing, Pharmacy, or a related field from an ...

Sitero LLC

Lead Clinical Trial Associate

Miami, FL · On-site

Lead Clinical Trial Associate Location: 3 days per week in our Coral Gables, Florida office. 2 days ... Bachelor's or Master's degree in Life Sciences, Nursing, Pharmacy, or a related field from an ...

Sitero LLC

Lead Clinical Trial Associate

Coral Gables, FL · Hybrid

$32 - $43.75/hr

Lead Clinical Trial Associate Location: 3 days per week in our Coral Gables, Florida office. 2 days ... Bachelor's or Master's degree in Life Sciences, Nursing, Pharmacy, or a related field from an ...

UAB

MANAGER-CLINICAL RESEARCH NURSING

Tampa, FL

$85K - $139K/yr

Currently licensed as a Registered Nurse (RN) by the Alabama Board of Nursing required. Preferences Hard skills: clinical trial, clinical research and data management, protocol compliance management ...

Charter Research

Clinical Research Coordinator

The Villages, FL · On-site

$20.75 - $27.75/hr

Communicate clinical trial issues to Sponsor and/or Contract Research Organization (CRO), Principal ... Licensed Practical Nurse (LPN), Registered Nurse (RN), or other medical licensure or certification ...

UAB

MANAGER-CLINICAL RESEARCH NURSING

Tampa, FL

$85K - $139K/yr

To assist with the management of the life cycle of the clinical trial as needed from study start-up ... Currently licensed as a Registered Nurse (RN) by the Alabama Board of Nursing required. Preferences

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Weekend Clinical Trial Rn information

What are the key skills and qualifications needed to thrive as a Weekend Clinical Trial RN, and why are they important?

To thrive as a Weekend Clinical Trial RN, you need a current RN license, clinical nursing experience, and a solid understanding of Good Clinical Practice (GCP) guidelines. Familiarity with clinical trial management systems, electronic data capture (EDC) tools, and protocol documentation is typically required. Strong attention to detail, organizational skills, and effective communication are vital soft skills for coordinating with research teams and ensuring regulatory compliance. These skills and qualities are crucial for maintaining patient safety, data integrity, and adherence to study protocols during weekend trial operations.

What are some unique challenges of working as a Weekend Clinical Trial RN, and how can I prepare for them?

As a Weekend Clinical Trial RN, you may encounter challenges such as limited onsite support, managing urgent protocol issues, and balancing patient care with strict research timelines. Since weekends often have fewer staff members present, strong communication and problem-solving skills are essential. To prepare, familiarize yourself with study protocols in advance, establish clear lines of communication with the principal investigator and other team members, and ensure you are comfortable with electronic data capture systems. Being proactive and organized will help you provide excellent patient care while maintaining compliance with research requirements.

What are Weekend Clinical Trial RNs?

Weekend Clinical Trial RNs are registered nurses who work primarily on weekends to support clinical research studies. Their responsibilities include administering investigational treatments, monitoring patient safety, collecting data, and ensuring protocol compliance. They collaborate with research teams, patients, and other healthcare providers to facilitate trials and maintain high standards of care. This role is crucial for studies that require continuous patient oversight and data collection outside of standard weekday hours.

What is the difference between Weekend Clinical Trial Rn vs Weekend Research Nurse?

AspectWeekend Clinical Trial RnWeekend Research Nurse
CredentialsRegistered Nurse (RN) license, clinical trial trainingRegistered Nurse (RN) license, research-specific training
Work EnvironmentClinical trial sites, hospitals, research facilitiesResearch centers, hospitals, clinical research units
Employer & IndustryPharmaceutical companies, research organizationsAcademic institutions, research organizations
Work ScheduleWeekend shifts, flexible hoursWeekend shifts, flexible hours

Both roles involve RN credentials and work in research settings, often during weekends. The main difference lies in the focus: Weekend Clinical Trial Rns primarily support clinical trial protocols, while Weekend Research Nurses may be involved in broader research activities. Both roles are essential in advancing clinical research and typically require similar certifications and work environments.

What cities in Florida are hiring for Weekend Clinical Trial Rn jobs? Cities in Florida with the most Weekend Clinical Trial Rn job openings:
Weekend Clinical Trial Rn jobs near you
Lead Clinical Trial Associate

Lead Clinical Trial Associate

Sitero LLC

Coral Gables, FL • On-site

$70K - $80K/yr

Full-time

Medical, Retirement, PTO

Posted 8 days ago

Job description

Sitero is a next-generation, technology-enabled Clinical Research Organization (CRO) serving the life sciences industry. We combine deep expertise across a diverse range of therapeutic areas with an innovative, tech-forward approach to clinical research - helping sponsors and sites get treatments to patients safer and faster. From early phase studies through Phase III clinical trials, our team delivers high-touch services and purpose-built technology with an unwavering commitment to ethics, compliance, and patient safety. With offices in the US, UK, Canada, and India, Sitero operates globally to support the full clinical program lifecycle.
Title: Lead Clinical Trial Associate
Location: 3 days per week in our Coral Gables, Florida office. 2 days per week from home
Function: Clinical Operations
Employment Type: Full Time
The Lead Clinical Trial Associate (Lead CTA) supports the execution of clinical trials by ensuring study documentation, site management activities, and data quality standards are maintained in alignment with ICH GCP, applicable regulations, and sponsor requirements. This is an excellent opportunity for an early-career clinical research professional to grow within a dynamic, technology-driven CRO environment.
Essential Duties & Responsibilities
  • Provide high-quality support in managing and overseeing clinical trials in accordance with ICH GCP guidelines, applicable regulations, company and sponsor SOPs, project plans, and local regulatory requirements.
  • Support Clinical Trial Managers with project-related activities and deliverables, including contract and budget activities as required.
  • Manage essential document collection and review throughout the study lifecycle; organize and maintain site Trial Master File (TMF) documents and site-related data in applicable clinical systems per record retention procedures.
  • Perform Informed Consent Form (ICF) customization in compliance with applicable guidelines and local regulatory requirements.
  • Support the setup, data entry, and quality control of clinical systems to ensure accuracy and integrity of study data.
  • Assist with new trial submissions, including protocol updates to Institutional Review Boards (IRBs) and Independent Ethics Committees (IECs).
  • Serve as EDC administrator, supporting site monitoring activities through EDC and eDTM/EDX applications.
  • Conduct ongoing risk assessments throughout the project lifecycle, including site process evaluations, follow-up on outstanding items, and timely escalation of issues.
  • Collaborate cross-functionally with internal departments - including Drug Safety, Regulatory, Data Management, and Biostatistics - to ensure seamless study execution.

Education & Experience
  • Bachelor's or Master's degree in Life Sciences, Nursing, Pharmacy, or a related field from an accredited university.
  • Minimum 5 years of experience in a CRO, pharmaceutical, or biotech environment; internship or co-op experience in clinical research considered.
  • Working knowledge of ICH GCP guidelines and clinical trial regulatory requirements.

Preferred Skills
  • Proficiency with Microsoft 365 (Word, Excel, Outlook, Teams).
  • Experience with EDC systems such as Medidata Rave or similar platforms.
  • Familiarity with Clinical Trial Management Systems (CTMS) and eTMF platforms.
  • Strong organizational skills and attention to detail with the ability to manage multiple priorities in a remote environment.
  • Effective written and verbal communication skills.

Commitments
  • Drivable distance to our Headquarter office in Coral Gables, Florida.
  • Standard schedule: 40 hours per week, Monday through Friday, with a one-hour lunch break.
  • Flexibility to work adjusted hours or shifts as study timelines and global team collaboration require.

Compensation & Benefits
Sitero offers a competitive compensation and benefits package including base salary, paid time off, and comprehensive healthcare and retirement benefits. Specific details will be discussed during the recruitment process.
Equal Opportunity Employer
Sitero is an equal opportunity employer and welcomes all job applicants. All qualified applicants will receive consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other factors prohibited by law.
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About Sitero

Sourced by ZipRecruiter

Industry

Scientific research and development services

Company size

11 - 50 Employees

Headquarters location

Miami, FL, US

Year founded

1999

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