Registered Nurse Clinical Trial - Portland, Maine
Location: Portland, Maine, United States
Job Category: Clinical Trial Nursing
Time Type: Part-time
Posted on: 4 Days Ago
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About ProPharma:
For over 20 years, ProPharma has been at the forefront of improving patient health by offering expert advice and consulting services to the biotech, pharmaceutical, and medical device industries. ProPharma’s partners benefit from a comprehensive model that supports clients throughout the entire product lifecycle, with expertise in regulatory sciences, clinical research, quality & compliance, and more.
Position Overview:
ProPharma is looking for a Registered Nurse Clinical Trial to join their team in Portland, Maine. This part-time role focuses on providing Direct Clinical Visit (DCV) services outside the investigator site, collaborating with the clinical research team, and ensuring patient safety and compliance throughout clinical trials.
Key Responsibilities:
Complete study-specific training, including GCP, IATA (dangerous goods), and study-specific training.
Provide quality DCV services at locations such as patients' homes, offices, or schools.
Work closely with the Director of Nursing and GoClinical Clinician Manager to solve complex clinical research and nursing challenges.
Document source information during DCVs following Good Documentation Practices and submit it to the project team promptly.
Report any issues or patient safety concerns to the GCPM, GCPC, and investigator site as necessary.
Physically capable of performing nursing tasks and lifting equipment up to 25lbs.
Access to 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.
Minimum of 2+ years of post-graduate experience.
Clinical research experience preferred.
Basic Life Support (BLS) Certification.
Preferred Skills:
Strong verbal and written communication skills in English.
Flexible and able to adjust to schedule and process changes with limited notice.
Willing to work after-hours or weekends if needed.
Proficient in MS Office suite and Google applications, with a willingness to gain proficiency in proprietary eSource software.
Excellent organizational skills, with the ability to multitask and prioritize based on protocol and visit parameters.
Consistently prepared for visit requirements and capable of troubleshooting equipment and supplies during visits.
Additional Information:
Candidates must be legally eligible to work in the United States.
Workplace Commitment:
ProPharma is dedicated to fostering diversity, equity, and inclusion within the workplace. We aim to create an environment where every employee feels empowered to bring their authentic self to work. As an Equal Opportunity Employer, we are committed to supporting innovative and entrepreneurial employees.
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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