Registered Nurse- Clinical Trial-Boise, Idaho

For the past 20 years, Pro Pharma 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. Pro Pharma 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, Pro Pharma 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 BOISE, IDAHO

• 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.
• Has reliable transportation to perform DCVs and transport necessary supplies and equipment (e.g., centrifuge, ECG machine, etc.).

• Education & Experience:
  
  Pediatric experience.
• Active, unencumbered RN licensure or certification in the 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 after‑hours 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 visit requirements as well as equipment and additional supplies for potential troubleshooting at the visit.

• All candidates must be legally eligible to work in the US.
• 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.
• All applications to roles at Pro Pharma 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 Pro Pharma 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. 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.
• Pro Pharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.