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Weekend Clinical Trial Rn Jobs in Melbourne, FL (NOW HIRING)

Aveanna Healthcare

Registered Nurse (RN)

Melbourne, FL · On-site

Days, nights, and weekend shifts- we will work with your availability! * 24/7 Local support from ... Must have and maintain an active, unencumbered license (RN) in the state in which the clinician ...

Adecco Colombia S.A.

RN Clinical Manager

Melbourne, FL · On-site

$90K - $100K/yr

Clinical Manager (RN) - Home Health $10,000 Sign-On Bonus Location: Melbourne, Florida (ZIP Code 32940) Job Type: Full-Time Schedule: Monday - Friday | 8:00 AM - 5:00 PM (In Office) Salary: $90,000 ...

Aveanna Healthcare

Registered Nurse (RN)

Rockledge, FL · On-site

Days, nights, and weekend shifts- we will work with your availability! * 24/7 Local support from ... Must have and maintain an active, unencumbered license (RN) in the state in which the clinician ...

Adecco

RN Clinical Manager

Melbourne, FL · On-site

$90K - $100K/yr

Clinical Manager (RN) - Home Health $10,000 Sign-On Bonus Location: Melbourne, Florida (ZIP Code 32940) Job Type: Full-Time Schedule: Monday - Friday | 8:00 AM - 5:00 PM (In Office) Salary: $90,000 ...

Adecco US, Inc.

RN Clinical Manager

Melbourne, FL · On-site

$90K - $100K/yr

Clinical Manager (RN) - Home Health $10,000 Sign-On Bonus Location: Melbourne, Florida (ZIP Code 32940) Job Type: Full-Time Schedule: Monday - Friday | 8:00 AM - 5:00 PM (In Office) Salary: $90,000 ...

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Weekend Clinical Trial Rn information

See Melbourne, FL salary details

$26

$57

$89

How much do weekend clinical trial rn jobs pay per hour?

As of Aug 27, 2026, the average hourly pay for weekend clinical trial rn in Melbourne, FL is $57.95, according to ZipRecruiter salary data. Most workers in this role earn between $47.02 and $65.29 per hour, depending on experience, location, and employer.

What is a Weekend Clinical Trial RN?

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 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 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 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 near Melbourne, FL are hiring for Weekend Clinical Trial Rn jobs?

Cities near Melbourne, FL with the most Weekend Clinical Trial Rn job openings:

Weekend Clinical Trial Rn jobs near you

Nurse Practitioner/Sub-Investigator

Tandem Clinical Research

FL • On-site

Full-time

Re-posted 15 days ago

Job description

The Sub-Investigator will serve as a key member of the clinical research team in a clinical trial setting. As an advanced practice medical professional, you will be responsible for ensuring the highest standards of patient care throughout the clinical trial process. Your primary role will involve conducting physical examinations, interpreting lab test results, overseeing patients' health, and performing essential clinical procedures while working closely with other healthcare professionals. You will be expected to provide both direct medical care and education to patients, as well as contribute to the advancement of clinical knowledge through research and professional collaboration.
Key Responsibilities
  • Perform physical examinations and assess patients' medical histories in a clinical trial setting.
  • Interpret and analyze lab test results to monitor patient health and make clinical decisions.
  • Oversee and monitor patient health status throughout the trial, ensuring patient safety and compliance with protocol requirements.
  • Educate patients and their families on the clinical trial process, including treatment plans and potential risks.
  • Administer medications and oversee the safe administration of investigational products, ensuring adherence to clinical protocols.
  • Perform venipuncture and phlebotomy procedures for laboratory testing as required by study protocols.
  • Prepare, initiate, and monitor IV infusions (including investigational product infusions), ensuring safe administration, accurate documentation, and appropriate patient monitoring.
  • Conduct medical procedures such as IV line placement, injections, and other tasks as required by the study protocol.
  • Monitor and provide safety observations during and after medication or infusion administration to ensure patient well-being and manage any adverse reactions.
  • Collaborate with the Principal Investigator and other members of the clinical trial team to ensure effective execution of study protocols.
  • Ensure proper documentation of clinical data in accordance with regulatory and ethical standards.
  • Maintain a clear, open line of communication with other healthcare professionals to ensure integrated, patient-centered care.
  • Participate in regular meetings and discussions to review patient progress, study outcomes, and other relevant clinical findings.
  • Stay informed on the latest developments in medical research and clinical practices, advancing personal and professional knowledge.

Additional Responsibilities
This job description includes core responsibilities but is not limited to the items listed above. The Sub-Investigator may be assigned additional duties as necessary to support the clinical trial and research efforts. These may include, but are not limited to, assisting in protocol design, supporting regulatory submissions, mentoring junior staff, and participating in educational and research initiatives.
Requirements
License/Certification Requirements
  • Nurse Practitioner Medical License or
  • Physician Assistant License

Qualifications
  • Proven experience in a clinical or healthcare setting, with a focus on patient care and medical research.
  • Strong phlebotomy and IV infusion skills, with demonstrated competency in patient monitoring during and after procedures.
  • Strong problem-solving skills and the ability to make sound clinical decisions.
  • Excellent communication skills, with the ability to effectively interact with patients, families, and other healthcare professionals.
  • Detail-oriented with a commitment to accuracy in medical documentation and patient monitoring.
  • Team player with a positive attitude and dedication to advancing clinical knowledge and patient care.
  • A strong passion for clinical research, patient advocacy, and advancing medical practices.

Preferred Skills
  • Previous experience in clinical trials or research settings.
  • Familiarity with regulatory guidelines and ethical practices in clinical research.
  • Ability to educate patients and staff on clinical protocols and research procedures.

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