Clinical Trial Nurse – Per Diem (Norwich, CT)
Location: Norwich, Connecticut
Employment Type: Part-time / Office-based
Job ID: R1514126
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Job Overview
We are seeking a skilled Clinical Trial Nurse to support and coordinate clinical research studies at our Norwich, CT site. The successful candidate will ensure clinical trials are executed in strict compliance with study protocols, Good Clinical Practice (GCP), International Conference on Harmonization (ICH) guidelines, sponsor Standard Operating Procedures (SOPs), and all applicable local and federal regulations. This role provides an opportunity to directly contribute to the advancement of innovative therapies while ensuring the safety and well-being of research participants.
Key Responsibilities
Coordinate and participate in clinical research studies, supporting investigators throughout all stages of study execution.
Review study protocols, source documents, case report forms, and electronic data capture systems to ensure accurate and compliant data collection.
Recruit, screen, and enroll patients, maintaining detailed logs of all study participants.
Orient research subjects on study objectives, procedures, and visit schedules.
Execute study visits and clinical procedures under the supervision of the Principal Investigator, including ECGs, lab sample collection, spirometry, vital signs, dose verification, cardiac telemetry monitoring, and questionnaire administration.
Prepare, handle, and process lab specimens in accordance with study requirements.
Monitor participant safety and report adverse events to the study team, Principal Investigator, and Institutional Review Boards (IRBs).
Maintain accurate source documentation adhering to GCP/ICH standards.
Provide guidance and training to site staff on study procedures, nursing best practices, and clinical research topics.
Support study audits, monitoring visits, and regulatory inspections, ensuring compliance with SOPs and regulatory requirements.
Participate in continuous quality improvement initiatives to optimize site performance, research processes, and study outcomes.
Assist in budget management, resource planning, and coverage scheduling for clinical research projects.
Qualifications & Experience
Current RN license required.
Minimum 2 years of experience in clinical research, healthcare, or related pharmaceutical environment.
Demonstrated knowledge of clinical trial processes, GCP, ICH, and regulatory requirements.
Strong clinical and therapeutic knowledge, with prior experience in executing complex study protocols.
Excellent organizational, communication, and problem-solving skills.
Ability to manage multiple priorities in a fast-paced research environment.
Experience with electronic data capture systems and regulatory documentation is preferred.
Travel & Work Requirements
Office-based role with occasional travel as required for training or site activities.
Compensation
Hourly rate: $50.00 – $60.00
Actual pay may vary depending on experience, location, and qualifications.
Eligible for additional benefits and incentives depending on assignment.
About IQVIA:
IQVIA is a global leader in clinical research services, commercial insights, and healthcare intelligence. We connect science and technology to accelerate the development and commercialization of innovative medical treatments, improving patient outcomes worldwide.
IQVIA is an equal opportunity employer. All qualified applicants will be considered without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.
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