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Clinical Trial Rn Jobs in Washington (NOW HIRING)

Guidehouse

Clinical Program Manager

Bethesda, MD · On-site

$85K - $141K/yr

Clinical Trial Operations Travel Required: None Clearance Required: Ability to Obtain Public Trust ... Master's degree in health and medical administrative services, nursing, or a related field.

Guidehouse

Clinical Program Manager

Bethesda, MD · On-site

$85K - $141K/yr

Clinical Trial Operations Travel Required: None Clearance Required: Ability to Obtain Public Trust ... Master's degree in health and medical administrative services, nursing, or a related field.

IQVIA

Infusion Nurse

Fairfax, VA · On-site

$37.75 - $50/hr

Oncology Clinical Trial Practices * Confirms informed consent is documented prior to performing any ... Current Registered Nursing License in the state the role is based in for RNs * OCN preferred. * IV ...

Medix

Oncology Registered Nurse

Bethesda, MD · On-site

$45 - $52/hr

Monitor patient status and side effects related to radiation therapy and ongoing clinical trial ... Active, unrestricted Registered Nurse (RN) license; current BLS certification. Skills * Technical ...

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Clinical Trial Rn information

See Washington salary details

$32

$70

$108

How much do clinical trial rn jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for clinical trial rn in Washington is $70.81, according to ZipRecruiter salary data. Most workers in this role earn between $57.45 and $79.76 per hour, depending on experience, location, and employer.

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.

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 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.

How to get into clinical trial registered nurse?

To become a clinical trial registered nurse, you typically need to hold a valid registered nurse (RN) license, gain experience in medical or research settings, and obtain specialized training in clinical research protocols. Certification through organizations like the Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SoCRA) can enhance job prospects. Strong communication skills, attention to detail, and familiarity with Good Clinical Practice (GCP) guidelines are also important.

What do clinical trial RNs do in clinical trials?

Clinical trial RNs coordinate and monitor patient care during clinical studies, ensuring protocol adherence and accurate data collection. They perform assessments, administer treatments, educate participants, and document outcomes while following regulatory and safety guidelines.

What are popular job titles related to Clinical Trial Rn jobs in Washington?

For Clinical Trial Rn jobs in Washington, the most frequently searched job titles are:

What job categories do people searching Clinical Trial Rn jobs in Washington look for?

The top searched job categories for Clinical Trial Rn jobs in Washington are:

Clinical Trial Rn jobs near you
Infographic showing various Clinical Trial Rn job openings in Washington as of August 2026, with employment types broken down into 92% Full Time, and 8% Part Time. Highlights an 92% In-person, and 8% Remote job distribution, with an average salary of $147,276 per year, or $70.8 per hour.

Clinical Program Manager

Guidehouse

Bethesda, MD • On-site

$85K - $141K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

This job post has expired 2 days ago. Applications are no longer accepted.

Guidehouse rating

8.0

Company rating: 8.0 out of 10

Based on 28 frontline employees who took The Breakroom Quiz

35th of 72 rated business consultants

Job description

Job Family:
Clinical Trial Operations
Travel Required:
None
Clearance Required:
Ability to Obtain Public Trust
What You Will Do:
We are currently searching for a Clinical Program Manger to support complex clinical research programs by coordinating investigators, research teams, oversight offices, regulatory agencies, partner institutions, and other key stakeholders to ensure studies run efficiently. This is a full-time opportunity located in Bethesda, MD.
  • Support complex clinical research portfolios by coordinating activities across investigators, research teams, regulatory bodies, and stakeholders in Bethesda, MD.
  • Provide end-to-end project management for clinical research, including planning, execution, monitoring, and closeout of studies and portfolios.
  • Develop and maintain project management plans, work plans, schedules, and performance metrics to track progress, timelines, deliverables, and resource allocation.
  • Coordinate operational and startup activities for clinical trials, including feasibility assessments, site coordination for multi-center trials, and study activation.
  • Facilitate project meetings, track action items, and ensure effective communication among stakeholders, leadership, and collaborating institutions.
  • Monitor study progress, enrollment metrics, and portfolio performance, identifying risks, barriers, and opportunities for improvement.
  • Support protocol development, IRB and regulatory submissions, amendments, and compliance with clinical trial requirements and milestones.
  • Develop and implement risk management strategies, including mitigation plans and resolution of operational, regulatory, and programmatic issues.
  • Support audits, inspections, and monitoring visits, ensuring readiness and compliance with applicable standards and guidelines.
  • Assist with financial management activities, including budget development, expenditure tracking, forecasting, and reporting.
  • Serve as a liaison between research programs, regulatory offices, and partners, preparing briefings, reports, and communication materials for leadership.
  • Support acquisition planning, contractor oversight, and strategic initiatives, including performance tracking and process improvement efforts.
  • Prepare and deliver routine and ad hoc reports such as portfolio status, risk management, financial summaries, regulatory tracking, and annual program reports.

What You Will Need:
  • Master's degree in health and medical administrative services, nursing, or a related field.
  • Minimum of FOUR (4) years of experience supporting clinical research programs.
  • Experience supporting complex clinical research portfolios and coordinating across stakeholders.
  • Experience with clinical trial management systems and research databases.
  • Experience with technology transfer agreements, clinical trial agreements, cooperative research and development agreements, or similar partnerships.
  • Experience supporting NIH, NCI, academic medical centers, or federally funded research programs.
  • Ability to manage multiple projects, timelines, and stakeholders simultaneously.
  • Must be able to obtain and maintain a Federal or DoD "public trust"; candidates must receive approved adjudication prior to onboarding with Guidehouse. Candidates with an active public trust or suitability are preferred.

What Would Be Nice To Have:
  • Certifications in any of the following: SOCRA, FAC-P/M, FAC-COR, and/or PMP Certification.
  • Strong project management, coordination, and communication skills.
  • Association of Clinical Research Professionals (ACRP) certification.
  • Experience in clinical trial design, feasibility assessments, and regulatory processes.
  • Experience supporting multi-site or multi-center clinical trials.

The annual salary range for this position is $85,000.00-$141,000.00. Compensation decisions depend on a wide range of factors, including but not limited to skill sets, experience and training, security clearances, licensure and certifications, and other business and organizational needs.
What We Offer:
Guidehouse offers a comprehensive, total rewards package that includes competitive compensation and a flexible benefits package that reflects our commitment to creating a diverse and supportive workplace.
Benefits include:
  • Medical, Rx, Dental & Vision Insurance
  • Personal and Family Sick Time & Company Paid Holidays
  • Parental Leave
  • 401(k) Retirement Plan
  • Group Term Life and Travel Assistance
  • Voluntary Life and AD&D Insurance
  • Health Savings Account, Health Care & Dependent Care Flexible Spending Accounts
  • Transit and Parking Commuter Benefits
  • Short-Term & Long-Term Disability
  • Tuition Reimbursement, Personal Development, Certifications & Learning Opportunities
  • Employee Referral Program
  • Corporate Sponsored Events & Community Outreach
  • Care.com annual membership
  • Employee Assistance Program
  • Supplemental Benefits via Corestream (Critical Care, Hospital Indemnity, Accident Insurance, Legal Assistance and ID theft protection, etc.)
  • Position may be eligible for a discretionary variable incentive bonus

About Guidehouse
Guidehouse is an Equal Opportunity Employer-Protected Veterans, Individuals with Disabilities or any other basis protected by law, ordinance, or regulation.
Guidehouse will consider for employment qualified applicants with criminal histories in a manner consistent with the requirements of applicable law or ordinance including the Fair Chance Ordinance of Los Angeles and San Francisco.
If you have visited our website for information about employment opportunities, or to apply for a position, and you require an accommodation, please contact Guidehouse Recruiting at 1-571-633-1711 or via email at RecruitingAccommodation@guidehouse.com. All information you provide will be kept confidential and will be used only to the extent required to provide needed reasonable accommodation.
All communication regarding recruitment for a Guidehouse position will be sent from Guidehouse email domains including @guidehouse.com or guidehouse@myworkday.com. Correspondence received by an applicant from any other domain should be considered unauthorized and will not be honored by Guidehouse. Note that Guidehouse will never charge a fee or require a money transfer at any stage of the recruitment process and does not collect fees from educational institutions for participation in a recruitment event. Never provide your banking information to a third party purporting to need that information to proceed in the hiring process.
If any person or organization demands money related to a job opportunity with Guidehouse, please report the matter to Guidehouse's Ethics Hotline. If you want to check the validity of correspondence you have received, please contact recruiting@guidehouse.com. Guidehouse is not responsible for losses incurred (monetary or otherwise) from an applicant's dealings with unauthorized third parties.
Guidehouse does not accept unsolicited resumes through or from search firms or staffing agencies. All unsolicited resumes will be considered the property of Guidehouse and Guidehouse will not be obligated to pay a placement fee.

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