Clinical Research Coordinator III – Registered Nurse (RN)
Location: Remote, Maryland, United States
Job ID: R-01329796
Job Type: Part-Time
Category: Clinical Research
Overview
Join a leading global Contract Research Organization (CRO) supporting the PPD® clinical research portfolio at Thermo Fisher Scientific. As a Clinical Research Coordinator III – RN, you will contribute to critical phase 1–3 clinical studies conducted within a military clinic environment, ensuring adherence to regulatory requirements and high-quality data collection.
This part-time, per-diem role requires onsite support in Silver Spring, Maryland with early-morning availability from 6:00 AM to 10:00 AM. The position is ideal for an experienced clinical research professional with strong nursing expertise and a commitment to regulatory excellence.
Key Responsibilities
Coordinate, organize, and prioritize activities for phase 1, 2, and 3 clinical and operational research studies.
Review and interpret clinical research protocols, ensuring strict compliance with applicable regulations and guidelines.
Support study documentation, source document design, visit scheduling, and study-specific planning.
Select and observe participants, assist in data analysis, and support reporting tasks.
Conduct data entry into case report forms (CRFs), resolve discrepancies, and maintain audit accuracy.
Manage investigational product accountability and administration according to study protocols.
Monitor data collection processes to ensure adherence to GCP, GLP, FDA, and other regulatory requirements.
Maintain documentation and ensure consistent quality across all clinical and operational processes.
Collaborate with team members while operating independently under general supervision.
Required Qualifications
Education & Licensing
Active Registered Nurse (RN) license in the state of Maryland.
Skilled in nursing procedures including administration of experimental vaccines and parenteral therapeutics in accordance with 21 CFR 11, 50, 54, 56, 312, and 314.
Basic Life Support (BLS – CPR/AED) certification.
Experience Required
Minimum 5 years of clinical research coordination experience, including work on FDA-regulated clinical trials.
Hands-on experience with clinical data systems such as REDCap and Inform.
Proven ability to work independently and collaboratively following technical training.
Strong communication, organizational, prioritization, and interpersonal skills.
Active certification in Clinical Research Coordination (ACRP or SoCRA).
Additional Requirements
Must be a U.S. citizen.
Must pass a comprehensive background check, including drug screening and physical examination.
Relocation assistance is not available.
Preferred Skills & Certifications
Advanced Cardiac Life Support (ACLS) certification.
Additional clinical research certifications (CCRP, CCRA).
Commission for Case Manager Certification (CCMC) preferred.
Work Environment
Laboratory and office setting requiring appropriate PPE (gown, gloves, lab coat, safety eyewear, etc.).
Standard Monday–Friday schedule with required early-morning availability.
Compensation
Estimated Pay Range (Maryland):
$38.46 – $44.23 per hour (CRA Level II)
This role may be eligible for a variable annual performance bonus according to company policies.
Benefits
Eligible U.S. colleagues have access to a comprehensive Total Rewards package, which may include:
National medical, dental, and vision plan options with health incentive programs
Employee assistance and family support programs
Tuition reimbursement and commuter benefits
Minimum 120 hours paid time off (PTO) plus 10 paid holidays
Paid parental leave (3 weeks bonding, 8 weeks caregiver leave)
Life, accident, and disability coverage
Competitive 401(k) retirement savings plan
Employee Stock Purchase Plan (ESPP) with discounted stock purchase options
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