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Clinical Research Nurse Rn Jobs (NOW HIRING)

Headlands Research

Clinical Research Nurse

Plymouth, MA · On-site

At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities ... Current and unencumbered license as a Registered Nurse (RN) in the state of Massachusetts required.

Denali Health

Clinical Research Nurse

Atlanta, GA · On-site

Current Registered Nurse (RN) license in the State of Georgia * Minimum 1-2 years of clinical ... Previous clinical research experience * CCRP (Certified Clinical Research Professional) or ACRP ...

Actalent

Clinical Research Nurse

Bucyrus, KS

Clinical Research Nurse I (Day Shift) The Clinical Research Nurse I plays a key role in ensuring ... Active Registered Nurse (RN) license with eligibility to practice in Kansas. * Ability to perform ...

Taphealthcare

Research Nurse Specialist

New York, NY

$109K - $125K/yr

... Registered Nurses looking to expand their careers in clinical research within a dynamic healthcare ... environment. Required Qualifications * Bachelor's Degree in Nursing (BSN) from an accredited ...

Saint Luke's Hospital of Kansas City

The Oncology Clinical Research Nurse, in addition to performing standard nursing duties, plays a ... Job Requirements Applicable Experience: 2 years Registered Nurse (MO) Multi-State - National ...

ICON

Clinical Research Nurse I

San Antonio, TX · On-site

Must hold a current and valid Registered Nurse (RN) license in the state of Texas. * Minimum of 1-2 years of clinical nursing experience, preferably in a research or academic healthcare setting, with ...

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Clinical Research Nurse Rn information

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$44

$62

How much do clinical research nurse rn jobs pay per hour?

As of Jul 24, 2026, the average hourly pay for clinical research nurse rn in the United States is $44.13, according to ZipRecruiter salary data. Most workers in this role earn between $36.30 and $52.40 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Clinical Research Nurse RN, and why are they important?

To thrive as a Clinical Research Nurse RN, you need a solid background in nursing practice, clinical research protocols, and regulatory compliance, generally supported by a nursing degree, RN license, and research experience. Familiarity with clinical trial management systems, electronic data capture (EDC) tools, and certifications like CCRC or CCRP is important. Attention to detail, strong organizational abilities, and effective communication skills help ensure accurate data collection and collaboration with research teams and participants. These competencies are critical for maintaining research integrity, patient safety, and successful study outcomes.

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

AspectClinical Research Nurse RnClinical Research Coordinator
CredentialsRN license, nursing certificationBachelor's degree, research training
Work EnvironmentHospitals, clinics, research sitesResearch sites, hospitals, clinics
Employer & IndustryPharmaceutical companies, hospitals, research institutionsResearch organizations, hospitals, academic institutions
Primary FocusPatient care, safety, and data collectionStudy coordination, protocol management

While both roles are integral to clinical research, the Clinical Research Nurse Rn primarily focuses on patient care and safety within research studies, utilizing nursing skills and certifications. The Clinical Research Coordinator manages study logistics, protocol adherence, and data collection. Both roles often collaborate but differ in daily responsibilities and required credentials.

What is a Clinical Research Nurse RN?

A Clinical Research Nurse RN is a registered nurse who specializes in conducting and managing clinical trials and research studies involving human participants. Their responsibilities include recruiting participants, administering study treatments, collecting data, ensuring compliance with research protocols, and maintaining patient safety. They work closely with physicians, researchers, and regulatory bodies to ensure the integrity and ethical conduct of the research. Clinical Research Nurses play a vital role in advancing medical knowledge and improving patient care through evidence-based research.

What are some common challenges Clinical Research Nurses (RNs) face when balancing patient care with study protocol requirements?

Clinical Research Nurses often navigate the challenge of delivering high-quality patient care while strictly adhering to complex clinical trial protocols. Balancing these responsibilities can be demanding, as patient needs must be met without compromising data integrity or regulatory compliance. Effective communication with multidisciplinary teams and meticulous attention to detail are crucial to ensure both patient safety and study accuracy. Many find that developing strong organizational skills and maintaining open lines of communication with investigators, coordinators, and patients helps manage these competing priorities successfully.
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Clinical Research Nurse Rn jobs near you
Clinical Research Nurse, RN

Clinical Research Nurse, RN

Headlands Research

San Juan, PR • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 15 days ago

Job description

At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.
Clinical Research Nurse (RN)
Location: San Juan, PR | Site Name: CMR Center | Full-Time
Are you an experienced clinical research professional with a passion for advancing medicine? Join a leading, integrated clinical research network dedicated to high-quality data, patient-centered care, and innovation in clinical trials.
We're seeking a Clinical Research Nurse (RN) for our clinical research site located in San Juan, PR. The ideal candidate has a background in hospital or private clinical practice, is passionate about patient-centered care, and thrives in a fast-paced, ambiguous, research-driven environment. This role requires a proactive self-starter who can navigate complex protocols with clinical judgment, independence, and attention to detail. Bilingual fluency in English and Spanish is essential.
Type: Regular Full-time Employee
Schedule: Mondays through Fridays, 8:30am - 4:30pm
Location: Onsite in San Juan, PR (no capabilities for remote or hybrid work)
Reports to: Clinical Research Manager
Benefits: Our benefits package for full-time employees includes health insurance (medical, dental, and vision), Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA), Paid Time Off (PTO), a variety of disability, accident, and life insurance options, as well as many more.
What We Offer
  • Competitive pay + annual performance incentives
  • Medical, dental, and vision insurance
  • 401(k) plan with company match
  • Paid time off (PTO) and company holidays
  • A mission-driven culture focused on advancing medicine and improving patient outcomes

Why Join Us?
You'll be part of a growing, mission-driven organization that values its people. At our core, we're committed to bringing innovative medical treatments to patients faster-while creating an environment where employees thrive. If you're passionate about clinical research and ready to make a difference, we'd love to hear from you.
Responsibilities:
  • Perform and document pediatric and adult phlebotomy procedures
  • Administer and document vital signs and clinical assessments
  • Support all phases of patient interaction including screening, enrollment, dosing, and follow-ups
  • Act as clinical support during study visits-monitor, document, and report on patient status and adverse events
  • Manage specimen handling, labeling, storage, and timely shipment according to protocol
  • Provide clinical oversight for study-related procedures to ensure safety and compliance
  • Coordinate and schedule research visits and procedures with precision and patient sensitivity
  • Review and interpret study protocols through a clinical lens to anticipate patient care needs
  • Communicate effectively with investigators, monitors, sponsors, and internal teams
  • Support study recruitment and patient outreach strategies
  • Maintain and organize source documentation and regulatory binders
  • Prepare for monitoring visits and assist during sponsor or regulatory audits
  • Other duties as needed to support study execution

Requirements:
  • Fluent in English and Spanish (written and verbal) required
  • Current and unencumbered license to practice as a Registered Nurse in Puerto Rico required
  • Minimum of 6 years of experience in a clinical setting (hospital or private practice) required
  • Minimum of 4 years drawing blood from both pediatric and adult patients required
  • Solid understanding of Good Clinical Practice (GCP) and/or willingness to undergo training
  • Comfort working within protocol-driven environments with shifting timelines
  • Demonstrated ability to operate autonomously and take initiative within a small, agile team
  • Proficient with electronic medical records, clinical data entry, and laboratory documentation
  • Exceptional organizational and multitasking skills
  • Strong interpersonal skills and compassionate bedside manner
  • Prior experience in clinical research or investigational trials is a plus
  • Familiarity with FDA, ICH-GCP, and HIPAA compliance standards a plus
  • Experience preparing for and interacting with clinical trial monitors a plus

Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver's license information, etc) via email or messenger tools, or for a financial deposit of any kind.
Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.
Need Assistance?
Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

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