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Weekend Clinical Trial Rn Jobs (NOW HIRING)

We are seeking experienced Registered Nurses to conduct in-home visits and support clinical trial patients participating in groundbreaking research studies. This per diem opportunity offers flexible ...

RN - Weekend Clinical

South Bend, IN ยท On-site

$55.32 - $62.84/hr

Registered Nurse (RN) - Weekend Clinical Southfield Village | Greencroft Communities Base Pay: $36.88-$41.89/hour based on experience Plus all weekend hours are paid at Time and a Half! ($55.32/hr ...

New

Registered Nurse (RN) Weekend Clinical Southfield Village | Greencroft Communities Base Pay: $36.88$41.89/hour based on experience Plus all weekend hours are paid at Time and a Half! ($55.32/hr-$62 ...

New

Clinical Trial Associate

Plainsboro, NJ ยท On-site

$70K - $123K/yr

... weekends. This position is located in Plainsboro, NJ and required to work onsite 5 days per week ... Clinical trial experience within a pharmaceutical, biotechnology, CRO and/or healthcare setting ...

Clinical Trial Associate

Plainsboro, NJ ยท On-site

$70K - $123K/yr

... weekends. This position is located in Plainsboro, NJ and required to work onsite 5 days per week ... Clinical trial experience within a pharmaceutical, biotechnology, CRO and/or healthcare setting ...

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Weekend Clinical Trial Rn information

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$28

$62

$96

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

As of Jul 16, 2026, the average hourly pay for weekend clinical trial rn in the United States is $62.52, according to ZipRecruiter salary data. Most workers in this role earn between $50.72 and $70.43 per hour, depending on experience, location, and employer.

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 are hiring for Weekend Clinical Trial Rn jobs? Cities with the most Weekend Clinical Trial Rn job openings:
What are the most commonly searched types of Clinical Trial Rn jobs? The most popular types of Clinical Trial Rn jobs are:
What states have the most Weekend Clinical Trial Rn jobs? States with the most job openings for Weekend Clinical Trial Rn jobs include:
Interim Clinical Trial RN - 7/6/2026

Interim Clinical Trial RN - 7/6/2026

Azad, Inc

San Jose, CA โ€ข On-site

$4.8K - $5.4K/wk

Other

Medical, Dental, Vision, Retirement

Posted 10 days ago


Job description

Healthcare Executive Placements, Inc. (HCEPInc) is seeking an Interim Clinical Trial RN for a W2 Contract position based in San Francisco, California.
Schedule: 5x8 Day, Day Shift, 8am-4:30pm
Assignment Duration: 13 Weeks with high likelihood of extending
Location: San Francisco, CA (base) - Travel required between several nearby facilities.
Weekly compensation: Between $4,827 - $5,430 (all-in), with flexibility in how the package is structured based on candidate needs. Compensation may include a combination of taxable wages, per diems (if eligible), and reimbursements.
Benefits: Paid sick leave, Paid holidays, Co-paid medical, dental, and vision insurance, Cafeteria plan access and 401(k) retirement plan.
Summary:
The Clinical Trials Nurse I (CTN-1) is a novice level position which, under the guidance and supervision of the Principal Investigator (PI) and clinical trials administrative management, assists in ensuring that the integrity and quality of the clinical trial (s) are maintained and conducted in accordance with federal, state and local regulations, Institutional Review Board (IRB) approvals, and the organizations policies and procedures. With direction from the PI, this position coordinates research activities. This position is also responsible for protecting the health, safety, and welfare of research participants.
Travel required between facilities San Francisco, Redwood City, and San Rafael.
Qualifications:
Minimum of a diploma from an accredited nursing school required.
High School Diploma or General Education Development (GED) required.
Minimum two (2) years of clinical nursing experience in a hospital, clinic or similar health care setting within the last three (3) years required (Bachelor's degree may be substituted for one (1) year work experience).
Clinical Research Professional Certificate within 12 months of hire from Society of Clinical Research Associates OR Clinical Research Associate Certificate within 12 months of hire from The Association of Clinical Research Professionals.
Registered Nurse License (California) required.
Basic Life Support required.
Additional Requirements:
Must be proficient in electronic health systems and databases used in research environment, or willingness to learn and demonstrate proficiency within six months of hire.
Demonstrate effective written, verbal, and interpersonal communication skills.
Attention to detail and accuracy.
Ability to manage multiple tasks with time deadlines.
Demonstrate prioritization and organizational skills.
Proficient in medical terminology.
Demonstrate basic drug calculation skills.
Demonstrate problem-solving skills.
Demonstrate nursing competency skills per scope of practice (i.e., phlebotomy, performing vital signs, nursing assessments, urine dipstick reading, pregnancy test reading, performing EKG, etc.) with certification if applicable.
Other (specific to relevant therapeutic area).
Knowledge of GCP, federal, state, and local regulations including HIPAA and KP policies and procedures.
Must be able to work in a Labor/Management Partnership environment.
Preferred Qualifications:
Clinical trials research experience preferred.
Must be dependable, punctual, detail-oriented, and able to follow detailed protocols precisely.
Must be able to work well independently as well as part of a larger multi-disciplinary research team.
Experience with word-processing and spreadsheet software programs preferred.
Proficiency with Microsoft Office products (Word, Excel, and PowerPoint) and Adobe Acrobat software highly desirable.
About Healthcare Executive Placements Inc. (HCEPInc.):
HCEPInc. values diversity - in backgrounds and in experiences.
Since our inception, we have witnessed how our diverse workforce has thrived while contributing to the increases in innovation and advancements in the client organizations we serve.
HCEPInc. is committed to Diversity, Equity & Inclusion and is striving to build an even more diverse, inclusive team that reflects the people and communities where we live and work.
HCEPInc. is an equal opportunity employer that considers and employs qualified individuals based upon job related qualifications regardless of race, color, sex, religion, creed, physical or mental disability, veteran's status, sexual orientation, national origin, age, or any other status protected under applicable local, state, or federal law.
HCEPInc. takes affirmative action to employ and advance in employment qualified employees and applicants who are disabled, disabled veterans, recently separated veterans, Armed Forces services medal veterans, and other protected veterans.
HCEPInc. is a Certified Minority Owned Business and OFCCP compliant.
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