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Full Time Clinical Trial Rn Jobs (NOW HIRING)

Ardelyx

Clinical Trial Associate

Newark, CA

$86K - $105K/yr

The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in the execution of ... Ability to travel as needed The anticipated annualized base pay range for this full-time position ...

Braveheart Bio

Clinical Trial Manager

San Francisco, CA · On-site +1

$140K - $170K/yr

At least 4+ years of relevant experience with a BS or BA in a relevant scientific discipline or an RN (2- or 3-year certificate) * Relevant clinical trial experience in the pharmaceutical or health ...

Verastem

Clinical Trial Associate

Boston, MA · On-site

$86K - $100K/yr

Bachelor's degree or nursing degree is required. Scientific/health care field preferred, but not ... clinical trial vendor). * Relevant experience in clinical research or related field. * Adequate ...

Novocure

Clinical Trial Lead

Wayne, PA · On-site

$147K - $190K/yr

Clinical Trial Lead Hybrid / Full Time / Chesterbrook, PA At Novocure, we're working to extend the ... Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field. * 5-7+ years of clinical ...

Prometrika LLC

Clinical Trial Manager

Cambridge, MA · On-site

$140K - $168K/yr

Bachelor's degree in life sciences, nursing, pharmacy, public health or related field is required ... clinical trial operations * Demonstrated experience managing multiple studies, sites and vendors ...

ARTBIO

Senior Clinical Trial Manager

Cambridge, MA · On-site +1

SummaryThe Senior Clinical Trial Manager will lead the day-to-day activities in a clinical trial ... Bachelor's or Master's degree in Life Sciences, Nursing, Pharmacy, or a related field. * 5 to 8 ...

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All JobsClinical Trial Rn JobsFull Time Clinical Trial Rn Jobs

Full Time Clinical Trial Rn information

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How much do full time clinical trial rn jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for full time 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 is the difference between Full Time Clinical Trial Rn vs Clinical Research Coordinator?

AspectFull Time Clinical Trial RnClinical Research Coordinator
CredentialsRegistered Nurse (RN) license, clinical trial trainingBachelor's degree, research training, sometimes certification
Work EnvironmentHospitals, clinics, research sites, hospitalsResearch sites, hospitals, clinics
Employer & IndustryPharmaceutical companies, research organizations, hospitalsResearch institutions, hospitals, CROs
Job FocusPatient care, administering trial protocols, data collectionStudy coordination, patient recruitment, data management

While both roles are vital in clinical research, a Full Time Clinical Trial RN primarily provides patient care and ensures protocol adherence from a nursing perspective. In contrast, a Clinical Research Coordinator manages study logistics, patient recruitment, and data collection. Both roles often collaborate but differ in their core responsibilities and required credentials.

What cities are hiring for Full Time Clinical Trial Rn jobs? Cities with the most Full Time 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 Full Time Clinical Trial Rn jobs? States with the most job openings for Full Time Clinical Trial Rn jobs include:
Full Time Clinical Trial Rn jobs near you

Clinical Trial Associate

Ardelyx

Newark, CA

$86K - $105K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 11 days ago

Job description

Ardelyx is a commercial-stage biopharmaceutical company focused on redefining treatment approaches for patients with significant unmet medical needs. By combining scientific innovation with a collaborative, purpose-driven culture, we strive to create meaningful impact for patients.
 
Team Ardelyx is united by a shared mission and guided by our core values: Passionate, Fearless, Dedicated, and Inclusive.
 
We foster an inclusive environment where employees are respected, supported, and empowered to make an impact — both within our company and in the lives of patients we serve..

 

Position Summary:

The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in the execution of assigned clinical trials, ensuring operational excellence, compliance with ICH-GCP and applicable regulatory requirements, and adherence to study timelines. The CTA contributes across all phases of the clinical trial lifecycle, from study start-up through close-out, and is responsible for the timely execution of study activities and deliverables in alignment with clinical development objectives and corporate goals.
 
Responsibilities:
  • Provide operational support for assigned clinical trial(s) across all phases of the study lifecycle, including start-up, conduct and close-out activities
  • Assist Clinical Trial Managers (CTMs) and other senior team members with day-to-day study activities to ensure study milestones and timelines are achieved
  • Track and follow up on study action items through resolution, escalating issues as appropriate
  • Develop, maintain and reconcile study trackers including but not limited to protocol deviations, adverse events, site training, enrollment metrics, and key study milestones
  • Perform data verification and reconciliation of study trackers against EDC, CTMS, and other clinical systems to ensure data accuracy and completeness
  • Support CTMS and other clinical system activities, including data entry, quality and validation activities as required
  • Author, format, update, and route study documents, plans, templates and training materials for review and approval
  • Review quality check, upload, file, and reconcile documents to eTMF in accordance with regulatory guidance, internal SOPs and TMF Reference Model standards
  • Coordinate document review workflows, training distribution, and collection of required documentation from internal teams and sites
  • Prepare and maintain study agendas, meeting minutes, action item logs, and study status reports while facilitating effective communication across cross-functional teams and external stakeholders
  • Contribute to health authority inspection readiness by providing requested documents.
  • Ensure study activities are conducted in compliance with ICH-GCP, applicable regulations, study protocols, and internal policies and procedures

Qualifications:

  • Bachelor’s degree in scientific or related field with 2+ years of experience in Clinical Operations, clinical research or healthcare, or equivalent experience
  • Working knowledge of the clinical trial lifecycle, from protocol development through study close-out
  • Familiarity with ICH-GCP guidelines, clinical trial documents, and applicable regulatory requirements
  • Experience with clinical trial systems such as EDC, CTMS and eTMF platforms, preferred
  • Proficiency with Microsoft Office applications, including Word, Excel, PowerPoint, and Outlook
  • Strong organizational skills with the ability to manage multiple priorities and maintain attention to detail in a fast-paced environment
  • Ability to work independently on routine assignments while exercising sound judgment and seeking guidance on more complex issues
  • Strong written and verbal communication skills, with demonstrated ability to collaborate effectively within cross-functional teams
  • Experience with Smartsheet or similar project management tools is a plus
  • Ability to travel as needed 

The anticipated annualized base pay range for this full-time position is $86,000 - $105,000. Ardelyx utilizes industry data to ensure that our compensation is competitive and aligned with our industry peers. Actual base pay will be determined based on a variety of factors, including years of relevant experience, training, qualifications, and internal equity. The compensation package may also include an annual bonus target and equity awards, subject to eligibility and other requirements.     

Ardelyx also offers a robust benefits package to employees, including a 401(k) plan with generous employer match, 12 weeks of paid parental leave, up to 12 weeks of living organ and bone marrow leave, equity incentive plans, health plans (medical, prescription drug, dental, and vision), life insurance and disability, flexible time off, annual Winter Holiday shut down, and at least 11 paid holidays.

 
Ardelyx is an equal opportunity employer.
 
We do not accept unsolicited resumes from search firms, or recruiters or similar vendors. Any such unsolicited resume submitted to any employee or through Company's career site without a valid, signed search agreement signed by Company's authorized representative will be deemed the property of the company, and no fees will be paid in the event of a hire. Company will have the right to hire any such candidate at its discretion without any financial obligation or fee owed to the vendor. Any verbal or written communication with a Company employee outside of this process will not be considered a binding agreement.

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