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Clinical Trial Rn Jobs (NOW HIRING)

CareDx, Inc.

Clinical Trial Manager

Brisbane, CA · On-site

  • Medical

  • Retirement

  • PTO

Bachelor's degree in life sciences, health sciences or equivalent degree/experience; RN or pharmaceutical experience preferred but not required. * Minimum of 4 years of clinical trial management and ...

Icon plc

Clinical Trial Assistant

San Francisco, CA · Hybrid

$56K - $70K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Clinical Trial Assistant (San Francisco, CA) ICON is a global healthcare intelligence and clinical ... e. nursing, medical or laboratory technology) from an accredited institution is preferred. * At ...

New

Icon plc

Clinical Trial Assistant

San Francisco, CA · Hybrid

$56K - $70K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Clinical Trial Assistant (San Francisco, CA) ICON is a global healthcare intelligence and clinical ... e. nursing, medical or laboratory technology) from an accredited institution is preferred. * At ...

New

Allucent

Clinical Trial Lead

Cary, NC · On-site +1

We are looking for a Clinical Trial Leader (CTL) to join our A-team (office-based*/remote). As a ... A degree in life sciences or nursing qualification preferred, but notrequired. * A minimum of5years ...

Clinovo

Clinical Trial Manager

Cambridge, MA · On-site

$175K/yr

The Clinical Trial Manager (CTM) plays a key role in the successful execution of clinical research ... Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related discipline; advanced degree ...

New

Allucent

Clinical Trial Lead

Cary, NC · Remote

We are looking for a Clinical Trial Leader (CTL) to join our A-team (office-based*/remote). As a ... A degree in life sciences or nursing qualification preferred, but not required. * A minimum ...

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 ...

IQVIA

Clinical Trial Nurse - Per Diem Fargo, ND

Fargo, ND · On-site

$50 - $60/hr

  • Medical

  • Life

Clinical Trial Nurse (Per Diem) - Fargo, ND Work Setting: Local Travel - In-Home Patient Visits Job ... Per Diem Are You a Registered Nurse Looking for a Flexible Opportunity in Clinical Research? Join ...

Actalent

Clinical Trial Specialist

Newark, NJ · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Clinical Trial Specialist coordinates and supports all aspects of clinical research studies ... Under the direction of the Research Nurse Clinician and physicians, ensure that IRB-approved ...

Novocure

Clinical Trial Lead

Manhattan, NY · Hybrid

$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 ...

IQVIA

Clinical Trial Nurse - Per Diem Fargo, ND

Fargo, ND · On-site

$50 - $60/hr

  • Medical

  • Life

Clinical Trial Nurse (Per Diem) - Fargo, ND Work Setting: Local Travel - In-Home Patient Visits Job ... Per Diem Are You a Registered Nurse Looking for a Flexible Opportunity in Clinical Research? Join ...

Novocure

Clinical Trial Lead

Philadelphia, PA · Hybrid

$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 ...

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Showing results 21-40

All JobsClinical Trial Rn Jobs

Clinical Trial RN information

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$28

$62

$96

How much do clinical trial rn jobs pay per hour?

As of Aug 13, 2026, the average hourly pay for 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.

How to get into clinical trial registered nurse roles?

To become a clinical trial registered nurse, candidates typically need a valid RN license, relevant clinical experience, and specialized knowledge of research protocols and regulations. Obtaining certifications such as Certified Clinical Research Professional (CCRP) can enhance qualifications. Experience in oncology, cardiology, or other specialized areas is often preferred, along with familiarity with Good Clinical Practice (GCP) guidelines and trial management tools.

What are the typical responsibilities of a Clinical Trial RN?

As a Clinical Trial RN, your daily tasks often involve screening and enrolling study participants, administering investigational treatments, monitoring patient responses, and accurately documenting all trial data. You will collaborate closely with physicians, research coordinators, and other healthcare professionals to ensure adherence to study protocols and patient safety guidelines. Additionally, you may educate patients and their families about trial procedures and follow up with them throughout the study. This role combines patient care with administrative and regulatory responsibilities, offering a dynamic and meaningful work environment.

What is a Clinical Trial RN?

A Clinical Trial RN (Registered Nurse) is a specialized nurse who plays a key role in clinical research studies. They assist in patient recruitment, administer treatments, monitor patient responses, and ensure adherence to study protocols. They also collect and document data, work closely with principal investigators, and ensure compliance with regulatory guidelines. Their role is essential in advancing medical research and improving patient care through clinical trials.

Can nurses work in clinical trials?

Yes, nurses, including registered nurses (RNs), often work in clinical trials by assisting with patient care, monitoring participants, and collecting data. They typically need relevant clinical trial training, knowledge of Good Clinical Practice (GCP), and sometimes certification to ensure compliance with regulatory standards.

What are the key skills and qualifications needed to thrive as a Clinical Trial RN?

To thrive as a Clinical Trial RN, you need a solid background in nursing practice, current RN licensure, and an understanding of clinical research protocols. Familiarity with clinical trial management systems, electronic data capture tools, and Good Clinical Practice (GCP) certification is often required. Strong attention to detail, superior organizational abilities, and effective communication skills make candidates excel in this role. These competencies are crucial to ensure patient safety, regulatory compliance, and the accurate collection and reporting of trial data.

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Clinical Trial RN jobs near you
Infographic showing various Clinical Trial Rn job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.

Clinical Trial Manager

CareDx, Inc.

Brisbane, CA • On-site

Full-time

Medical, Retirement, PTO

Re-posted 3 days ago

Job description

CareDx, Inc. is a leading precision medicine solutions company focused on the discovery, development, and commercialization of clinically differentiated, high-value healthcare solutions for transplant patients and caregivers. CareDx offers products, testing services, and digital healthcare solutions along the pre- and post-transplant patient journey, and is the leading provider of genomics-based information for transplant patients.
This position provides direction and operational leadership of the clinical research studies to ensure delivery on time. The Clinical Trial Manager (CTM) is responsible for the management of clinical trials from study start-up activities through the clinical study report. The CTM drives completion of all study deliverables, ensuring the highest level of data quality and compliance to quality standards and regulatory guidance; proactively identifies, communicates and resolves clinical study operational issues; and participates in process improvement initiatives as required.
Specific responsibilities include, but are not limited to:
  • Lead the end-to-end execution of CareDx clinical trials, including but limited to site identification, study start-up, study conduct, monitoring and closeout, with full accountability of study timelines, budget and metrics; study submission to IRB/ECs; study document development and review (training documentation, ICF, study specific plans, eCRF Guidelines, lab test requisitions, etc.), plans and managing study-specific meetings (e.g. Study Team Meetings, Investigator meetings, etc.)
  • Drive site activation, enrollment, and overall study performance while ensuring alignment with protocols, operational plans, and business objectives.
  • Proactively identify study risks (timeline, quality, and operational), lead mitigation planning and execution, and escalate issues effectively with clear action plans, defined ownership, and accountability.
  • Conduct internal review of investigator contracts and payments, as necessary.
  • Provide cross-functional leadership across Clinical Operations, Data Management, Medical Affairs and other functional areas serving as the central point of coordination to ensure clear roles, accountability, and seamless clinical trial execution.
  • Prepare and present project debriefings to Clinical Operations management and cross-functional teams.
  • Oversee Clinical Research Associates, CROs, central labs, and external vendors to ensure high-quality, timely, and cost-effective deliverables through established governance, KPIs, and performance management processes.
  • Champion operational excellence by standardizing study execution models, optimizing vendor management and reporting frameworks, and implementing scalable process improvements and SOPs.
  • Ensure data quality and inspection readiness through proactive data review, performance metric tracking, and close collaboration with monitoring and data management teams. Identify and mitigate risks across timelines, quality, and operations, driving effective escalation and resolution strategies.
  • Maintain strong communication with clinical sites and stakeholders, including oversight of site visits, study documentation, and reporting, while ensuring compliance with GCPs, regulatory requirements, and study protocols.
  • Support study administration activities such as site engagement, training, and product inventory management to ensure efficient and compliant study execution.
  • Ensure high-quality, inspection-ready documentation and study tracking through effective use of eTMF including oversight of TMF completeness, document quality, and real-time study status reporting.
  • Provide oversight and operational support for CTMS system and effective use of it for tracking study milestones, enrollment, monitoring activities, and performance metrics.
  • Directly leading and managing clinical operations personnel.

Minimum Qualifications
  • Education: Bachelor's degree in life sciences, health sciences or equivalent degree/experience; RN or pharmaceutical experience preferred but not required.
  • Minimum of 4 years of clinical trial management and 2+ years clinical research associate with on-site/remote clinical monitoring experience in the biotechnology/pharmaceutical/CRO industry.
  • Minimum of 2 years directly managing, coaching, and developing clinical operations professionals (e.g., Sr. CRAs, CRAs, CTAs, etc.), including workload management, performance development, and cross-functional collaboration.
  • Robust understanding of ICH/GCP, and knowledge of regulatory requirements.
  • Working knowledge of medical terminology.
  • Experience with medical laboratory testing and documentation of patient information.
  • Comfortable with technology and scientific/engineering principles.

Skills and Experience:
  • A critical thinker and capable of problem solving and aligning the priorities with study outcomes and timelines.
  • Strong clinical study/project management skills.
  • Excellent communication, written and organizational skills (ability to prioritize a number of tasks of varying complexity), along with problem solving, conflict resolution, leadership and team-building skills.
  • Ability to motivate and collaborated with teams at other functional departments.
  • Ability to work independently, take initiative, and meet company goals within timelines and budget.
  • Ability to mentor staff, drive accountability, manage priorities, and support the successful execution of clinical studies.
  • Able to work in a fast-paced environment with multiple competing tasks and demands, across time-zones.
  • Must have a sense of urgency about problem-solving and completing projects.
  • Ability to communicate with vendors and keep a high quality of clinical study.
  • Strong knowledge of FDA regulations and GCP.
  • Proficient in Microsoft Office (excel, word, outlook, power point), electronic data capture (EDC) software (Medrio, Medidata) and other platform related to electronic Trial Master File (eTMF), CTMS and safety report.

SCOPE OF WORK
  • Travel estimate 10-30% .
  • Operate within standard guidelines, but must engage in some independent decision-making.
  • Errors that are not quickly detected and rectified could have a significantly adverse effect on the quality of the study.
  • Works closely with other Clinical Research staff, as well as staff from other departments.

PREFERENCES
  • Experience with clinical studies involving organ transplantation.

Additional Details:
Every individual at CareDx has a direct impact on our collective mission to improve the lives of organ transplant patients worldwide. We believe in taking great care of our people, so they take even greater care of our patients.
Our competitive Total Rewards package for US Employees includes:
  • Competitive base salary and incentive compensation
  • Health and welfare benefits, including a gym reimbursement program
  • 401(k) savings plan match
  • Employee Stock Purchase Plan
  • Pre-tax commuter benefits
  • And more!
  • Please refer to our page to view detailed benefits at https://caredx.com/company/careers

In addition, we have a Living Donor Employee Recovery Policy that allows up to 30 days of paid leave annually to a full-time employee who makes the selfless act of donating an organ or bone marrow.
With products that are making a difference in the lives of transplant patients today and a promising pipeline for the future, it's an exciting time to be part of the CareDx team. Join us in partnering with transplant patients to transform our future together.
CareDx, Inc. is an Equal Opportunity Employer-vets/disabled, and participates in the E-Verify program. By proceeding with our application and submitting your information, you acknowledge that you have read our U.S. Personnel Privacy Notice and consent to receive email communication from CareDx. Certain jurisdictions require notice of how we use and protect your personal information. For more information, please read our Privacy Policy
The U.S. EEO posters are available here.
Note: We do not accept resumes from headhunters, placement agencies, or other suppliers that have not signed a formal agreement with us.
#LI-Remote
This is the anticipated base salary range for candidates who will work in Brisbane, California. The final salary offered to a successful candidate will be dependent on several factors that may include, but are not limited to, the type and length of experience within the job, the type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives and restricted stock units. CareDx is a multi-state employer, and this salary range may not reflect positions that work in other states.
San Francisco Bay Area Roles
$124,000-$155,000 USD
This is the anticipated base salary range in the United States. The final salary offered to a successful candidate will be dependent on several factors that may include, but are not limited to, the type and length of experience within the job, the type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives and restricted stock units. CareDx is a multi-state employer, and this salary range may not reflect positions that work in other states.
Remote: US only roles
$112,000-$140,000 USD

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