Registered Nurse-Clinical Trial-NY, NY

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 Complete study‑specific requirements for each assigned study, which may include GCP training, IATA (dangerous goods) training, and study‑specific training. Provide quality DCV services to patients at a location outside of the investigator site (e.g., home, office, school). Collaborate with the Director of Nursing and GoClinical Clinician Manager to apply clinical research and nursing practices to develop solutions to complex problems. Complete source documentation during DCVs following Good Documentation Practice and submit source to the project team in a timely manner. Communicate issues and patient safety concerns to GCPM, GCPC, and the investigator site as appropriate. Be physically able to perform assigned nursing tasks and lift equipment up to 25 lbs in weight. Have reliable transportation to perform DCVs and transport necessary supplies and equipment (e.g., centrifuge, ECG machine). Qualifications Active, unencumbered RN licensure or certification in the United States. Multistate practice/licensure preferred where applicable. Minimum 2+ years of post‑graduate experience. Basic Life Support (BLS) certification (preferred). Preferred Skills Ability to communicate in English, both verbal and written. Flexible and able to make quick accommodations to schedule changes, process changes, and travel on limited notice. Willingness to work after‑hours or weekends (preferred). Computer skills and experience; working knowledge of MS Office suite and Google applications. Willingness to gain expertise in proprietary eSource software. Organized and able to multitask; prioritize based on protocol and visit parameters. Consistent preparedness for specific visit requirements, equipment, and supplies for troubleshooting. Additional Information All candidates must be legally eligible to work in the United States. 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. As an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed. #J-18808-Ljbffr ProPharma