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Clinical Research Rn Jobs in Washington, DC (NOW HIRING)

Research Nurse Specialist

Bethesda, MD · On-site

$74K - $124K/yr

Coordinate clinical research activities to meet thestudyprotocol requirements and manage the ... Active, current license as a Registered Nurse in the United States, the Commonwealth of Puerto Rico ...

Research Nurse Specialist

Bethesda, MD · On-site

$74K - $124K/yr

Coordinate clinical research activities to meet thestudyprotocol requirements and manage the ... Active, current license as a Registered Nurse in the United States, the Commonwealth of Puerto Rico ...

Research Nurse Specialist

Bethesda, MD · On-site

$98K - $163K/yr

Coordinate clinical research activities to meet thestudyprotocol requirements and manage the ... Active, current license as a Registered Nurse in the United States, the Commonwealth of Puerto Rico ...

Research Nurse Specialist

Bethesda, MD · On-site

$98K - $163K/yr

Coordinate clinical research activities to meet thestudyprotocol requirements and manage the ... Active, current license as a Registered Nurse in the United States, the Commonwealth of Puerto Rico ...

Job Summary The Clinical Nurse must be knowledgeable of standard research and oncology care ... Current Registered Nursing License for the state the role is based in for RN's * Oncology ...

Job Summary The Clinical Nurse must be knowledgeable of standard research and oncology care ... Current Registered Nursing License for the state the role is based in for RN's * Oncology ...

Job Summary The Clinical Nurse must be knowledgeable of standard research and oncology care ... Current Registered Nursing License for the state the role is based in for RN's * Oncology ...

Clinical Research Coordinator - 257457

Potomac, MD · On-site

$25 - $33.25/hr

Clinical Research Coordinator * Contract Duration: Expected to end in January 2027; NO possibility ... May be the sole coordinator or work in collaboration with a research nurse on studies, responsible ...

As a Clinical Research Nurse (General RN), you will provide specialized direct care to patients participating in groundbreaking clinical trials. This role integrates traditional acute-care bedside ...

Job Title Research Nurse Concentric Methods is seeking an experienced Research Nurse to ... Work with staff to develop procedure manuals for clinical research protocols. * Work with staff to ...

Showing results 41-60

Clinical Research Rn information

See Washington, DC salary details

$20

$49

$71

How much do clinical research rn jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for clinical research rn in Washington, DC is $49.97, according to ZipRecruiter salary data. Most workers in this role earn between $41.11 and $59.33 per hour, depending on experience, location, and employer.

What is a clinical research RN?

Clinical Research Registered Nurses (Clinical Research RNs) are licensed nurses who specialize in conducting and coordinating clinical trials and research studies involving human participants. They collaborate with physicians, researchers, and study coordinators to ensure that research protocols are followed, participants are cared for safely, and all regulatory and ethical guidelines are met. Their duties include administering study medications, collecting data, monitoring patient responses, and educating participants about the study. Clinical Research RNs play a vital role in advancing medical knowledge and improving patient care through research.

How does a clinical research RN typically collaborate with other members of the research team?

A Clinical Research RN works closely with principal investigators, study coordinators, physicians, and data managers to ensure research protocols are followed accurately and patient safety is maintained. They are responsible for communicating patient progress, reporting adverse events, and coordinating care between departments. Regular team meetings and detailed documentation are essential to keep everyone informed and maintain compliance with regulatory standards. This collaborative environment helps ensure research studies run smoothly and efficiently.

What are the key skills and qualifications needed to thrive as a clinical research RN, and why are they important?

To thrive as a Clinical Research RN, you need a solid background in nursing, clinical trial protocols, and regulatory compliance, typically requiring an RN license and experience in research settings. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification is often expected. Excellent organizational, communication, and critical thinking skills help you coordinate studies, interact with participants, and collaborate with multidisciplinary teams. These competencies ensure the integrity of research data, patient safety, and successful execution of clinical trials.

What is the difference between Clinical Research Rn vs Clinical Research Coordinator?

AspectClinical Research RnClinical Research Coordinator
CredentialsRN license, possibly specialized certificationsTypically bachelor's degree, certifications like CCRP beneficial
Work EnvironmentHospitals, clinics, research institutionsResearch sites, hospitals, clinics
Job FocusPatient care, protocol adherence, data collectionStudy coordination, participant recruitment, data management

While both roles are involved in clinical research, the Clinical Research Rn primarily provides patient care and ensures protocol compliance from a nursing perspective. The Clinical Research Coordinator manages study logistics, participant recruitment, and data collection. Both roles require strong organizational skills, but the RN's focus is more on patient interaction, whereas the Coordinator handles study operations.

How to get into clinical research as a registered nurse?

To become a clinical research RN, obtain a valid nursing license and gain experience in patient care. Additional certifications such as Certified Clinical Research Professional (CCRP) or Good Clinical Practice (GCP) training can improve job prospects, and familiarity with research protocols and data management is beneficial.

What do clinical research RNs do in clinical research?

Clinical research RNs coordinate and monitor clinical trials by recruiting participants, collecting data, administering treatments, and ensuring compliance with study protocols and regulations. They often work closely with investigators, maintain accurate documentation, and may require certification such as CCRP. Their role is essential for the safe and effective conduct of research studies.
Infographic showing various Clinical Research Rn job openings in Washington, DC as of August 2026, with employment types broken down into 2% As Needed, 68% Full Time, 24% Part Time, and 6% Contract. Highlights an 81% Physical, 1% Hybrid, and 18% Remote job distribution, with an average salary of $103,969 per year, or $50 per hour.

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Job description

Clinical Nurse

The Clinical Nurse must be knowledgeable of standard research and oncology care practices. The Clinical Nurse advocates for patient safety and protocol integrity, adheres to patient care standards, and communicates effectively to ensure effective conduct of clinical trials and quality patient care.

Essential Duties and Responsibilities

Essential and other important responsibilities and duties may include but are not limited to the following:

Protocol Compliance
  • Adheres to applicable federal, state, and institutional regulations, policies, and procedures related to clinical research.
  • Complies with NEXT Oncology SOPs
  • Participates in providing timely, informative, and accurate communication with the interdisciplinary team to ensure protocol compliance and timeliness of protocol-related procedures
  • Collaborates with the PI, pharmacy, and other appropriate personnel to ensure proper use of and accountability for study drugs
Informed Consent
  • Identifies and intervenes to address barriers to effective informed consent discussions and decision making (e.g., literacy, capacity, language, distress, lack of time, therapeutic misconception)
  • Describes and abides by institutional policy and processes for informed consent
  • Assesses patient's understanding of the information provided during the informed consent process
  • Ensures timely re-consenting as needed by the physician investigator.
  • Confirms informed consent is obtained prior to performing any study specific tasks.
Management of Clinical Trial Patients
  • Provides complete patient assessment, including vital signs and pre-examination procedures
  • Gathers and assess objective and subjective data from the patient
  • Documents data and assessments accurately in the patient record
  • Assists the providers in all aspects of the consultation, treatment, procedures, and follow-up care
  • Records medical history and symptoms, completing documentation in the medical record
  • Coordinates patient care, acting as a liaison with other departments and organizations
  • Provides patient education before and after procedures, use of medical devices and equipment, and prescriptions
  • Triage of calls for urgent appointments, referrals for patient consults and resting, insurance precertification, and documentation
  • Educates the patient and family regarding clinical condition and/or disease process
  • Ensures timely completion of protocol-required events and other requirements (e.g. pharmacokinetics or-dynamics, scans, study visits, QOL.)
  • Assesses individual patients for physical, psychosocial, and financial factors that could impact adherence with study requirements and implement interventions as necessary
  • Evaluates patient's adherence to and documentation of self-administered protocol agents and the return of such agents
  • Collaborates with the investigator to determine disease response as defined by the protocol and communicates findings to the study team and other care providers
  • Evaluates patient's adherence to and documentation of self-administered protocol agents and return of such agents
  • Collaborates with the investigator to determine if any treatment schedule or drug dose modification is necessary and communicates findings to the study team and other care providers
  • Ensures appropriate communication between clinical and research staff related to patient-specific care needs
  • Ensures evidence-based symptom management as permitted by the protocol
  • Patient health counseling and instruction, including meeting with families and caregivers
  • Medication reconciliation, management, patient compliance, inventory, education
  • Ensures regulatory compliance with OSHA guidelines, CLIA regulations, HIPAA medical privacy guidelines
Documentation and Document Management
  • Documents all patient encounters in the legal medical record per licensure and institutional requirements
  • Obtains documents from outside providers or laboratories that are needed
  • Assesses documentation or discrepancies and ensures that inaccurate or discrepant documentation is addressed in the medical record or other source documents
  • Maintains the privacy and confidentiality of patient's source documents
  • Other duties as assigned
Required Education and Experience
  • Current BLS and ACLS or obtained within 90 days of employment
  • Current Virginia Registered Nursing License for RN's
  • Oncology experience preferred
  • Clinical trial experience preferred

Why Join Us? At NEXT Oncology (an Avacare Business), you'll be part of a mission-driven team that values collaboration, precision, and patient safety. Our team is known for its supportive culture, strong communication, and commitment to excellence in clinical research.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law.

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $62,700.00 - $156,700.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.