Registered Nurse-Clinical Trial-Alexandria, VA

ProPharma Group; Alexandria (VA); Sur place; USD 80 000 - 110 000; Plein temps

Résumé du poste

ProPharma Group is seeking a Registered Nurse to support clinical research visits conducted outside investigator sites. You will collect data, ensure patient safety, and collaborate with leadership to implement nursing practices in study activities.

The role requires US RN licensure and BLS certification, with flexibility for after-hours or weekend work and potential travel. A hybrid work model is available, with some office collaboration preferred.

Qualifications

• Active RN license in the US and BLS certification required or preferred.
• Clinical research experience is preferred but not mandatory.
• Strong documentation and data-entry abilities essential.

Responsabilités

• Completes study-specific requirements and training for assigned studies.
• Provides DCV services to patients outside investigator sites.
• Collaborates with Nursing Director to apply clinical research practices.
• Documents source data per Good Documentation Practice and submits timely.
• Communicates issues and patient safety concerns to stakeholders.
• Physically able to perform nursing tasks and lift up to 25 lbs.

Connaissances

RN licensure

Clinical nursing

English (written & spoken)

Documentation skills

Formation

RN licensure (US)

BLS Certification

Outils

MS Office

Google Apps

eSource software

Description du poste

For the past 25 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.

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.).

Qualifications

• Education & Experience Active, unencumbered RN licensure or certification in US Multistate practice/licensure preferred where applicable Minimum 2+ years post-graduate experience Clinical research experience preferred Basic Life Support (BLS) Certification Preferred Skills 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.
• 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.
• 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.

Additional Information

• All candidates must be legally eligible to work in the US #LI-mk1

All applications will be treated on their own merit and candidates will not be at any advantage or disadvantage based on their proximity to an office.

All applications to roles at ProPharma are personally reviewed by a member of our recruitment team.

We do not rely on AI screening tools to support our hiring process.

You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not.

Whilst ProPharma supports remote working, we also recognise the value that comes from in person collaboration. As such, we encourage any new hires that are based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager.

We celebrate our differences and strive to create a workplace where each person can be their authentic self.

We are committed to diversity, equity, and inclusion.

Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits.

With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.