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Clinical Trial Rn Remote Jobs in Texas (NOW HIRING)

IQVIA

Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... Master's degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work (or ...

IQVIA

Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... Master's degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work (or ...

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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?

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 RN Remotes 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 August 2026, with employment types broken down into 80% Full Time, 13% Part Time, and 7% Contract. Highlights an 100% Remote job distribution.

Clinical Trial Liaison (CTL), Ophthalmology (Nationwide/US-Based)

TMAC (The Medical Affairs Company (TMAC))

Dallas, TX • Remote

Full-time

Posted 10 days ago

Job description

Clinical Trial Liaison (CTL), Ophthalmology (Nationwide/US-Based)

Serving as a value-added resource and extension of the Company, the Clinical Trial Liaison (CTL) will support the Company’s Ophthalmology clinical trial pipeline. The CTL will serve as a clinical trial and clinical program subject matter expert and problem solver to help study sites optimize their study performance. The CTL will work full time to help sites address challenges in study delivery that could impact the Company’s study or program goals.

This role involves compliant collaboration with KOLs, investigators, research staff members and CRO to build strong professional partnerships, provide credible scientific expertise, and serve as a field-based extension of the clinical trial team to support ongoing studies.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Site and Investigator Partnerships

  • Create investigator engagement plans to support site-specific recruitment, site identification and/or selection
  • Provide clinical trial liaison support to site investigators involved in sponsored studies including protocol support, screening barriers, and clinical trial recruitment and retention
  • Generate feasible, time-bound, prioritized action plans to address any barriers identified at clinical sites, document the plan and meet with the sites regularly to measure progress
  • Serve as a liaison to internal R&D and Clinical Operations functions to ensure the effective support of PIs
  • Collection of key medical insights from PIs to inform refinement of strategies

Building Company & Pipeline Advocacy

Through compliant scientific exchange, build and maintain professional relationships with external stakeholders to expand research, company advocacy, and educational partnerships

Expertise Management and Cross Functional Support

  • Maintain awareness of and access to internal and external information sources available to support high-quality scientific exchanges with HCPs
  • Develop/increase knowledge of relevant medical literature and critical appraisal of scientific publications
  • Maintain knowledge base and scientific expertise on all assigned disease areas and products
  • Develop and update knowledge of applicable pharmaceutical guidelines and regulations. Code of Ethical Practices and company policies
  • Provide scientific input and participate in local medical and cross functional initiatives
  • Build scientific relationships with key thought leaders, healthcare professionals, investigators and their teams, government organizations, and patient and provider advocacy groups
  • Collect key strategic insights from top research KOLs and HCPs to support strategic initiatives
  • Maintain working knowledge of regulatory and ethical requirements for all initiatives.

QUALIFICATIONS:

  • Knows how clinical sites operate, and has a history of helping study sites solve practical problems on clinical trials
  • Healthcare/science background inclusive of PharmD, PhD and MD, OD (or equivalent) required.
  • Clinical background in the area of Ophthalmology, with expertise in retinal diseases required
  • 5+ years of clinical research or clinical research support experience within academic, healthcare system or industry setting (e.g., clinical research coordinator, research manager, clinical research associate, study coordinator, research director) is required. Qualified individuals will have a strong familiarity and experience with clinical research and study site logistics.
  • Frequent travel is required. Availability to travel up to 50% of time
  • Availability to attend meetings on holidays and weekends
  • Clean and valid driver’s license

Salary offers to be determined based on industry experience, education, and therapeutic expertise.

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