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Clinical Research RN - Overnights

Full-time

Stark Pharma Solutions Inc

Stark Pharma Solutions Inc. is a global consulting and staffing partner established in 2014, serving the Pharmaceutical, Medical Device, Biotech, and IT industries across the USA, Canada, and India. We provide specialized consulting and staffing solutions across Quality & Validation, Regulatory Affairs, R&D, Manufacturing, Supply Chain, Project Management, and IT, with a focus on delivering tailored solutions that drive growth, operational excellence, and long-term client success.
Research Nurse II

We are seeking an experienced Research Nurse II to support Phase I clinical research studies. The role involves providing nursing care to study participants, monitoring patient safety, performing clinical assessments, managing adverse events, and maintaining accurate study documentation in compliance with clinical research protocols and regulatory guidelines.
Participate in the execution of Phase I clinical research study protocols.
Maintain the safety, well-being, and confidentiality of study participants.
Perform nursing procedures, including starting IVs, wound dressings, and clinical assessments.
Coordinate study-related nursing activities with the Principal Investigator, study physicians, screening teams, data systems, and other personnel.
Identify and help resolve source data discrepancies and documentation issues.
Follow study protocols, departmental SOPs, Good Clinical Practice (GCP), ICH guidelines, and applicable regulatory requirements.
Participate in quality improvement and compliance initiatives.
Assist with training new nursing personnel and monitor their progress.
Complete required orientation and training across all three shifts.
Active Illinois nursing license.
Minimum 1 year of nursing experience; new graduates are not eligible.
ICU experience preferred; telemetry or emergency room experience is also desirable.
Strong nursing skills, including IV starts, patient assessments, dressings, and computer-based documentation.
Familiarity with clinical research protocols, informed consent, source documentation, and GCP guidelines is beneficial.
Ability to work night shifts, including every other weekend.

Vacancy posted 10 hours ago
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