Registered Nurse Clinical Trial - Parkesburg, PA
Location: Parkesburg, PA, United States
Job Category: Clinical Trial Nursing
Time Type: Part-time
Posted on: 8 Days Ago
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About ProPharma:
For over two decades, ProPharma has provided expert advice and consulting services that support the biotech, pharmaceutical, and medical device industries. ProPharma partners with clients throughout the entire product lifecycle, offering a range of solutions from regulatory sciences and clinical research to pharmacovigilance and R&D technology.
Position Overview:
ProPharma is seeking a Registered Nurse Clinical Trial to join their team in Parkesburg, PA. This part-time position will be responsible for providing Direct Clinical Visit (DCV) services to patients outside of the investigator site, collaborating with the clinical research team, and ensuring compliance with clinical trial protocols.
Key Responsibilities:
Complete study-specific training, including GCP, IATA (dangerous goods), and study-specific requirements.
Provide high-quality DCV services at patient locations outside of the investigator site (e.g., home, office, or school).
Work with the Director of Nursing and GoClinical Clinician Manager to address complex clinical research and nursing issues.
Accurately document source data during DCVs in compliance with Good Documentation Practices, submitting the information to the project team on time.
Communicate any issues or patient safety concerns to GCPM, GCPC, and investigator site as needed.
Physically capable of performing nursing tasks and lifting up to 25lbs of equipment.
Reliable transportation for performing DCVs and transporting necessary equipment (e.g., centrifuge, ECG machine).
Qualifications:
Active, unencumbered RN licensure or certification in the United States.
Multistate practice/licensure preferred.
At least 2+ years of post-graduate nursing experience.
Clinical research experience preferred.
Basic Life Support (BLS) Certification.
Preferred Skills:
Strong verbal and written communication skills in English.
Ability to adapt to schedule and process changes with limited notice.
Willingness to work after-hours or weekends, as needed.
Proficient in MS Office suite and Google applications, with a willingness to gain expertise in proprietary eSource software.
Highly organized with the ability to multitask and prioritize visits according to protocol and visit parameters.
Preparedness for specific visit requirements and troubleshooting equipment and supplies as needed.
Additional Information:
All candidates must be legally eligible to work in the United States.
Workplace Commitment:
ProPharma fosters a diverse and inclusive environment, encouraging employees to express their authentic selves. We provide a safe and empowering space for innovation and collaboration, and we are committed to diversity, equity, and inclusion within our workplace.
Additional Notes:
ProPharma does not accept unsolicited resumes from recruiters or third-party agencies.
No phone calls or emails regarding this posting, please.
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