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Registered Nurse- Clinical Trial-Fort Belvoir, Va

Propharma
Propharma
2+ years
preferred by company
10 Jan. 20, 2026
Job Description
Job Type: Part Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Registered Nurse – Clinical Trial (Fort Belvoir, VA)

Job ID: JR 8874
Location: Fort Belvoir, Virginia, United States
Employment Type: Part-Time
Travel Requirement: Local travel for patient visits


About ProPharma

For over 20 years, ProPharma has partnered with biotech, pharmaceutical, and medical device organizations worldwide to advance scientific breakthroughs and bring innovative therapies to patients. Through our advise–build–operate model, we provide end-to-end clinical research, regulatory, and safety solutions. Our expertise spans clinical trial execution, nursing support, regulatory compliance, pharmacovigilance, medical information, and R&D technology, enabling clients to accelerate high-profile programs with precision and quality.


Position Overview

We are seeking a Registered Nurse (RN) to support clinical trial operations through Direct-to-Patient Care Visits (DCVs) at locations outside the investigator site, including patient homes, schools, or offices. This role requires a detail-oriented, adaptable, and clinically skilled RN with pediatric experience who can apply nursing and clinical research practices to complex scenarios while maintaining high-quality standards and patient safety.

Note: Candidates must reside in or near Fort Belvoir, VA.


Key Responsibilities

  • Conduct study-specific procedures for assigned clinical trials, including GCP training, IATA (dangerous goods) certification, and study-specific onboarding.

  • Provide Direct-to-Patient Care Visits (DCVs) at locations outside the investigator site, ensuring patient safety and adherence to study protocols.

  • Collaborate with the Director of Nursing and GoClinical Clinician Manager to apply clinical expertise to problem-solving and protocol implementation.

  • Complete source documentation during DCVs according to Good Documentation Practices and submit accurately to the project team in a timely manner.

  • Communicate issues, deviations, and patient safety concerns promptly to project managers, coordinators, and investigator sites.

  • Ensure all clinical equipment (e.g., centrifuge, ECG machine) is prepared, transported safely, and utilized correctly.

  • Maintain physical capability to perform nursing tasks and lift up to 25 lbs of equipment.


Required Qualifications

  • Education & Licensure: Active, unencumbered RN licensure or certification in the United States. Multistate licensure preferred.

  • Experience: Minimum 2+ years of post-graduate nursing experience; clinical research experience preferred.

  • Specialty Experience: Pediatric care experience is required.

  • Certifications: Current Basic Life Support (BLS) certification.

  • Technical Skills: Working knowledge of MS Office, Google applications, and willingness to learn proprietary eSource systems.

  • Language Skills: Proficiency in English (verbal and written).


Preferred Skills

  • Flexibility to accommodate schedule changes, travel with limited notice, and work evenings or weekends if needed.

  • Ability to multitask and prioritize activities based on protocol and patient visit requirements.

  • Strong organization and preparedness, including troubleshooting for clinical visits.

  • Excellent communication and interpersonal skills to interact with patients, families, and project teams.


Additional Information

  • Must be legally eligible to work in the United States.

  • Position requires local travel to patient locations within Fort Belvoir, VA.

  • Hybrid work is supported for administrative or documentation tasks; in-person patient visits are required.


Why Join ProPharma

At ProPharma, we prioritize diversity, equity, and inclusion and provide a supportive environment for professional growth. Employees are empowered to collaborate, innovate, and deliver high-quality patient care. Our commitment to integrity, accountability, and excellence ensures that every team member contributes to advancing healthcare globally.

Apply now to be part of a dynamic clinical research team, supporting critical studies and improving patient outcomes.