Clinical Trial Nurse – Per Diem
Norwich, Connecticut | Office-Based | Job ID: R1514126**
Position Overview
A leading global clinical research organization is seeking a Per Diem Clinical Trial Nurse to support and coordinate clinical research studies conducted at the Norwich, Connecticut site. This role involves ensuring all study activities comply with study protocols, Good Clinical Practice (GCP), sponsor standard operating procedures (SOPs), and all applicable regulatory guidelines.
This position is ideal for experienced clinical nursing professionals who possess strong organizational skills, working knowledge of clinical trial operations, and a commitment to safeguarding study participants.
Key Responsibilities
Clinical Research Operations
Provide clinical research support to investigators throughout all phases of assigned clinical studies.
Review study protocols, case report forms, source documentation, and electronic data capture systems.
Manage regulatory submissions and ethics documents required by the FDA and other governing authorities.
Recruit, screen, and enroll eligible participants; maintain accurate screening and enrollment logs.
Educate study participants on study procedures, timelines, and protocol expectations.
Clinical Procedures & Safety Oversight
Conduct study visits and perform delegated clinical procedures under the supervision of the Principal Investigator.
Handle laboratory activities including specimen preparation, storage, and logistics coordination.
Monitor participant safety, document adverse events, and report findings to investigators and IRBs as required.
Serve as a primary point of contact for participant questions and study-related concerns.
Data Quality & Study Compliance
Maintain high-quality source documentation aligned with GCP and ICH standards.
Participate in data quality checks, query resolution, and ongoing documentation reviews.
Assist with site readiness for monitoring visits, audits, and regulatory inspections.
Ensure strict adherence to SOPs, study protocols, and site guidelines.
Team Collaboration & Training
Attend routine study meetings with investigators and site staff to track progress and responsibilities.
Support training initiatives for new site personnel on study-specific procedures.
Maintain accurate training records and ensure compliance with required certifications.
Provide mentorship and oversight to junior site staff to uphold protocol and SOP compliance.
Participate in continuous improvement initiatives to support study operations and site performance.
Skills & Competencies
Strong clinical judgment and ability to perform advanced clinical procedures such as ECG, spirometry, lab sample collection, vital signs assessment, dose verification, telemetry monitoring, and questionnaire administration.
Excellent communication skills and the ability to advocate for study participants.
Strong attention to detail, documentation accuracy, and understanding of research compliance standards.
Ability to work effectively in a fast-paced, collaborative research environment.
Experience & Qualification Requirements
Active Registered Nurse (RN) license required.
Minimum 1–2 years of clinical experience, preferably within a clinical research setting.
Experience with GCP/ICH guidelines and familiarity with clinical trial processes preferred.
Prior exposure to regulatory documentation, participant recruitment, and study coordination is an advantage.
Ability to perform complex clinical procedures and manage participant interactions with professionalism.
Compensation
Hourly rate: $50.00 – $60.00
Final compensation may vary based on experience, education, location, and other job-related factors.
Additional incentives, bonuses, health, and welfare benefits may be available depending on employment status.
About the Employer
A global leader in clinical research, healthcare intelligence, and advanced data analytics, committed to accelerating medical innovation and improving patient outcomes. The organization provides equal employment opportunities to all qualified individuals regardless of race, gender, identity, disability, veteran status, or any protected category.
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