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Clinical Trial Rn Remote Jobs (NOW HIRING)

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Senior Clinical Trial Manager

Blue Bell, PA · Remote

Senior Clinical Trial Manager - Remote, US ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As ...

ARTBIO

Senior Clinical Trial Manager

Cambridge, MA · On-site +1

Perform clinical research site activities, which can include onsite or remote monitoring, co ... Bachelor's or Master's degree in Life Sciences, Nursing, Pharmacy, or a related field. * 5 to 8 ...

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Senior Clinical Trial Manager

Blue Bell, PA · On-site +1

Senior Clinical Trial Manager, Biotech - Remote, US ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

IQVIA

Trial Delivery Manager, Multi TA

Durham, NC · Remote

Clinical Trial Management & Central Trial Oversight (FSP Model) Home Based Remote Role - East Coast ... Bachelor's degree (or equivalent) in Life Sciences (e.g., Biology, Chemistry, Nursing, Pharmacy)

IQVIA

Trial Delivery Manager, Multi TA

Boston, MA · Remote

Clinical Trial Management & Central Trial Oversight (FSP Model) Home Based Remote Role - East Coast ... Bachelor's degree (or equivalent) in Life Sciences (e.g., Biology, Chemistry, Nursing, Pharmacy)

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How much do clinical trial rn remote jobs pay per hour?

As of May 30, 2026, the average hourly pay for clinical trial rn remote 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 are the key skills and qualifications needed to thrive as a Clinical Trial RN Remote, and why are they important?

To thrive as a Clinical Trial RN Remote, you need a robust background in clinical nursing, research protocols, and a valid RN license, often supported by experience in clinical trials or research settings. Familiarity with electronic data capture (EDC) systems, remote monitoring tools, and certifications such as CCRC (Certified Clinical Research Coordinator) are commonly required. Strong organizational skills, attention to detail, and effective communication are essential soft skills for managing remote patient interactions and complex documentation. These skills are vital to ensure protocol compliance, data integrity, and patient safety while working independently in a remote environment.

What are some common challenges Clinical Trial RNs face when working remotely, and how can they be addressed?

Clinical Trial RNs working remotely often face challenges such as maintaining effective communication with study teams, ensuring patient safety during remote monitoring, and navigating varying time zones for global trials. To address these, leveraging secure digital platforms for documentation and meetings, establishing clear protocols for virtual patient assessments, and scheduling regular check-ins with research coordinators are essential. Proactive collaboration and strong organizational skills help ensure study compliance and high-quality patient care, even from a distance.

What is a Clinical Trial RN Remote?

A Clinical Trial RN (Registered Nurse) Remote is a nurse who works off-site to support clinical research studies. Their responsibilities include monitoring patient progress, collecting and managing data, ensuring compliance with study protocols, and providing patient education—all from a remote location. They often communicate with patients, study teams, and healthcare providers via phone, email, or telehealth platforms. This role allows RNs to contribute to clinical research without being physically present at a trial site, offering flexibility and broader access to research opportunities.

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

AspectClinical Trial Rn RemoteClinical Research Coordinator
CredentialsRegistered Nurse (RN) license, clinical trial experienceBachelor's degree, often in health or science fields; certification optional
Work EnvironmentRemote, often from home, coordinating patient care and dataOn-site or hybrid, managing study logistics and participant recruitment
Employer & IndustryPharmaceutical companies, CROs, research institutionsResearch sites, hospitals, clinics, pharmaceutical companies
Search & Comparison IntentFocus on remote nursing roles in clinical trialsFocus on study coordination and site management

While both roles are involved in clinical research, Clinical Trial Rn Remote primarily involves remote nursing duties, patient monitoring, and data collection, whereas Clinical Research Coordinator handles study logistics, participant recruitment, and site management, often on-site. Understanding these differences helps job seekers find roles aligned with their skills and preferences.

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

Senior Clinical Trial Manager

Barrington James

Manhattan, NY • Remote

Full-time

Posted 9 days ago

Job description

Senior Clinical Trial Manager – IBD Biotech - US-based, Key Early Hire Location: United States (Remote/Flexible) About the Role My client, a pioneering small biotech developing transformative therapies for IBD, is seeking a Senior Clinical Trial Manager to join their growing team. This is a unique opportunity to take a leadership role as a trial lead , shaping clinical strategy and execution from the ground up, and becoming one of the first key hires in the U.S. In this role, you will have direct impact on the design, management, and delivery of early- to mid-stage clinical trials.

You will collaborate closely with cross-functional teams—including clinical operations, regulatory, medical affairs, and external vendors—to ensure trials are executed efficiently, on time, and in compliance with regulatory standards. Key Responsibilities Lead and manage clinical trials in IBD from start-up through close-out, acting as the trial lead for pivotal studies. Oversee timelines, budgets, and operational plans to ensure successful execution of studies.

Serve as primary point of contact for internal teams, external vendors, and clinical sites. Support regulatory submissions, safety reporting, and quality compliance initiatives. Contribute to the development of clinical protocols, informed consent forms, and study-related documentation.

Mentor and guide junior team members as the organization grows. Travel up to 30% Qualifications Bachelor's degree in life sciences, nursing, pharmacy, or related field (advanced degree preferred). 5–8+ years of clinical trial management experience , ideally in gastroenterology, IBD, or immunology.

Demonstrated success as a trial lead on complex, multi-site studies. Strong knowledge of GCP, FDA/EMA regulations, and clinical trial operational best practices. Excellent leadership, communication, and problem-solving skills.

Comfortable in a dynamic, fast-paced startup environment and excited by the opportunity to make a high-impact contribution. Why This Role is Exciting Be one of the first U.S. hires at an innovative biotech with a clear mission to improve outcomes for IBD patients.

Direct influence on trial design and clinical strategy. Work in a collaborative, entrepreneurial environment where your contributions are highly visible. Competitive compensation package with equity options.

Send your resume to cburns@barringtonjames.com #J-18808-Ljbffr

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