Registered Nurse- Clinical Trial-Fairfax, VA

ProPharma Group • Raleigh, NC

3d

About The Position

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs. MUST RESIDE IN OR NEAR FAIRFAX, VA Key Responsibilities: Completes study-specific requirements for each assigned study which may include GCP training, IATA (dangerous goods) training, and study-specific training. Provides quality DCV services to patients at a location outside of the investigator site (e.g., home, office, school). Collaborates with Director of Nursing and GoClinical Clinician Manager to apply clinical research and nursing practices to develop solutions to complex problems. Completes source documentation during DCVs following Good Documentation Practice and submits source to project team in a timely manner. Communicates issues and patient safety concerns to GCPM, GCPC, and investigator site as appropriate. Physically able to perform assigned nursing tasks and lift equipment up to 25lbs in weight. Access to a reliable transportation to perform DCVs and transport necessary supplies and equipment (e.g., centrifuge, ECG machine, etc.).

Requirements

• Pediatric experience
• Active, unencumbered RN licensure or certification in US
• Minimum 2+ years post-graduate experience
• Ability to communicate in English (both verbal and written).
• Flexible and able to make quick accommodations to schedule changes as well as process changes and to travel with limited notice.
• Organized and able to multitask; prioritizes based on protocol and visit parameters.
• Consistent preparedness for specific visits requirements as well as equipment and additional supplies for potential trouble shooting at the visit.

Nice To Haves

• Multistate practice/licensure preferred where applicable
• Clinical research experience preferred
• Basic Life Support (BLS) Certification
• Ability to work afterhours or weekends preferred.
• Computer skills/experience.
• Working knowledge of MS Office suite and Google applications.
• Willingness to gain expertise in the use of propriety eSource software.

Responsibilities

• Completes study-specific requirements for each assigned study which may include GCP training, IATA (dangerous goods) training, and study-specific training.
• Provides quality DCV services to patients at a location outside of the investigator site (e.g., home, office, school).
• Collaborates with Director of Nursing and GoClinical Clinician Manager to apply clinical research and nursing practices to develop solutions to complex problems.
• Completes source documentation during DCVs following Good Documentation Practice and submits source to project team in a timely manner.
• Communicates issues and patient safety concerns to GCPM, GCPC, and investigator site as appropriate.
• Physically able to perform assigned nursing tasks and lift equipment up to 25lbs in weight.
• Access to a reliable transportation to perform DCVs and transport necessary supplies and equipment (e.g., centrifuge, ECG machine, etc.).

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: No Education Listed
• Number of Employees: 251-500 employees