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Clinical Trial Rn Remote Jobs in Texas (NOW HIRING)

Renalogic

Clinical Nurse Coordinator (LPN)

Dallas, TX · On-site +1

$58K - $68K/yr

US, fully remote with minimal travel Schedule:Mostly standard business hours, with some flexing to ... You'll collaborate with RNs, providers, and interdisciplinary teams to ensure care plans, referrals ...

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Clinical Trial Rn Remote information

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 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 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 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 are the most commonly searched types of Clinical Trial Rn jobs in Texas? The most popular types of Clinical Trial Rn jobs in Texas are:
What cities in Texas are hiring for Clinical Trial Rn Remote jobs? Cities in Texas with the most Clinical Trial Rn Remote job openings:
Clinical Trial Rn Remote jobs near you
Infographic showing various Clinical Trial Rn Remote job openings in Texas as of July 2026, with employment types broken down into 87% Full Time, and 13% Contract. Highlights an 100% Remote job distribution.
Clinical Research Manager III (Remote Position)

Clinical Research Manager III (Remote Position)

Artech Information System LLC

Fort Worth, TX • On-site, Remote

Contractor

Re-posted 13 days ago

Job description

Company Description

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.

Job Description

Job Description:
Accountable for all aspects of assigned clinical trials. Lead the Clinical Trial Team, who is responsible for planning, conducting and reporting of clinical trials. Author robust protocols with scientific rigor and quality. Trial conduct must be efficient, with seamless execution and timely reporting.
Lead and matrix manage the global multidisciplinary Clinical Trial Team who is responsible for planning, conducting and reporting on all clinical trials within Development, including trials for Proof-of-Concept and Registration. Each Clinical Manager leads 2 or more clinical trial teams for studies of medium to high complexity in support of one or more projects.
Contribute medical/scientific/feasibility input for the development of the protocol synopsis. Collaborate with the Medical Advisors to ensure country feedback is adequately integrated into the protocol.
Independently ensure quality and timely execution of a clinical trial within timeline and budget
Forecast trial resource needs. Accountable for the development, management and tracking of trial budget. Obtains approval for trial budget. Accountable for accuracy of trial information in all trial databases and tracking systems. Manages ongoing study budget.
Write scientifically rigorous protocols aligned with the approved protocol synopsis.
Lead clinical trial team to select countries and sites.
Ensure investigational product supply.
Ensure Health Authority and IRB/IEC submission and approval.
Ensure all auxiliary documents, including manual of procedures, informed consent template, investigator brochure, statistical analysis plan, data validation plan, etc. are written in high quality and available.
Define clinical outsourcing specifications for clinical trial vendors (labs, reading centers, etc.). Work with Procurement to identify vendors.
Define scope of work and contract requirements for clinical trial vendors. Oversees vendor conduct of tasks.
Ensure implementation of standard data collection modules, where possible or obtains approval for deviation.
Track trial progress and milestones.
Resolve issues within the clinical trial team or elevates issue to appropriate teams and governance committee.
Ensure ongoing data quality review (masked review).
Ensure data cleaning and database lock.
Ensure reporting of results to Management, Clinical Team and Core Team.
Arrange and lead Clinical Trial Team Meetings and responsible for writing minutes
Active participant of the Clinical Team under the leadership of the Clinical Lead (CL).
Contribute to the development of clinical sections of regulatory documents like Investigators Brochures, briefing packets, safety updates, IND/NDA submission documents, responses to Health Authorities questions.
Responsible for implementation of best practices and standards for trial management, including sharing lessons learned.

Qualifications
Skills:
Ability to establish clear directions and set stretch objectives
Aligns and energizes team members behind common objectives
Excellent people and communication skills
Organizational awareness to operate in a cross-functional team
Builds support from others in situations with no direct authority
Ability to embrace and communicate change
Well organized / solid project management skills
Customer/Quality Focus
Scientific thinking allowing to identify bias and validity issues
Establishes effective relationships with customers and gains their trust and respect
Conduct of clinical studies
Experience in running clinical studies independently without significant supervision
Ability to proactively identify issues, respond appropriately and provide guidance for pro-active resolution
Solid understanding of the clinical trial regulations (GCP, FDA, EMA, ICH, ISO etc.)
Education:
University degree in Medical Science or equivalent education required. Advanced degrees (e.g., MD, PhD, O.D., PharmD) are preferred.
9+ years in clinical research or relevant scientific, industry, therapeutic or geographic experience
Relevant industry experience includes experience in planning and execution of clinical studies in various phases and geographies
Solid understanding of the integrated development process of medical devices and/or pharmaceuticals


Additional Information
Warm Regards
Neha Sharma
Lead Recruiter
Artech Information Systems LLC
360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960
Office: 973.967.3437 | Fax:  973.998.2599
Artech logo

About Artech

Sourced by ZipRecruiter

Artech is a leading IT staffing and consulting company based in Morristown, NJ, US. Since its foundation in 1992, Artech has mastered in complementing human expertise with technology and business acumen to produce world-class staffing solutions. The company caters to diverse industry sectors, including financial services, healthcare, telecommunication, energy and utilities, supply chain, and retail. It provides IT consulting, project management, professional and staff augmentation, and managed staffing services. Artech's mission is to provide exceptional IT staffing services to its clients by comprehending their business needs and then crafting a customized staffing strategy. Its notable achievement includes being recognized as one of the largest IT staffing companies in the U.S, according to Staffing Industry Analysts (SIA).

Industry

Recruiting and staffing services

Company size

10,000+ Employees

Headquarters location

Morristown, NJ, US

Year founded

1992

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