Clinical Research Coordinator III – Registered Nurse (RN)
Job ID: R-01329796
Employment Type: Part-Time / Per Diem
Work Mode: Remote with On-Site Support
Location: Maryland, United States (On-site support in Silver Spring, MD)
Category: Clinical Research | Government Clinical Trials | Nursing Research
Experience Required: Minimum 5 years in clinical research coordination
Schedule: Monday–Friday | 6:00 AM – 10:00 AM
About the Organization
Our Clinical Research Services team plays a critical role in advancing therapies that address complex global health challenges. As part of a leading global Contract Research Organization (CRO), the team supports the PPD® clinical research portfolio and delivers high-quality, compliant clinical trials across laboratory, digital, and decentralized environments.
With studies conducted in more than 100 countries, the organization provides the scientific expertise, infrastructure, and regulatory excellence needed to bring innovative therapies to market efficiently and safely.
Role Overview
The Clinical Research Coordinator III – RN is a senior-level clinical research role supporting a U.S. government customer within a military clinical research setting. This position is per diem and non-benefited, requiring early morning availability and strong experience in FDA-regulated clinical trials.
The role is ideal for an experienced Registered Nurse with advanced clinical research coordination expertise, strong regulatory knowledge, and the ability to operate independently in high-compliance environments.
Key Responsibilities
Clinical Research Coordination
Coordinate and manage Phase I, II, and III clinical and operational research studies
Review, interpret, and ensure adherence to research protocols and regulatory requirements
Organize and manage clinical research documentation, data, and study materials
Select, observe, and support study participants and assist with data analysis and reporting
Data & Compliance Management
Enter, review, and reconcile data in CRFs, audit records, and clinical trial management systems
Maintain investigational product accountability and proper administration
Monitor data collection processes to ensure compliance with FDA, GCP, GLP, and government regulations
Participate in source document creation, SSP development, visit scheduling, and materials planning
Operational Oversight
Oversee experiment scheduling and data collection timelines
Apply clinical judgment to plan and accomplish research objectives under general supervision
Collaborate effectively with multidisciplinary research teams and government stakeholders
Education, Licensure & Certifications
Required
Active Registered Nurse (RN) license to practice in the state of Maryland
U.S. Citizenship required
Ability to pass comprehensive background check, drug screening, and physical examination
Basic Life Support (BLS – CPR/AED) certification
Proven competency in administering experimental vaccines and parenteral therapeutics in compliance with 21 CFR 11, 50, 54, 56, 312, and 314
Experience Requirements
Minimum 5 years of experience in clinical research coordination within FDA-regulated trials
Hands-on experience with clinical trial management systems and databases (e.g., REDCap, Inform)
Demonstrated ability to work independently and collaboratively following limited technical training
Strong communication, organizational, and prioritization skills
Experience maintaining regulatory compliance in government or military research settings preferred
Preferred Qualifications
Maintenance of Certification in Clinical Research Coordination (ACRP or SoCRA)
Advanced Cardiac Life Support (ACLS) certification
Clinical research certifications such as CCRP or CCRA
Commission for Case Manager Certification (CCMC)
Work Environment
Combination of laboratory and office settings
Use of personal protective equipment (PPE) including lab coats, gloves, safety glasses, and hearing protection
Early morning work schedule with consistent attendance expectations
Compensation & Benefits
Estimated Hourly Pay (Maryland): USD 38.46 – 44.23
Eligibility for variable annual bonus based on company and individual performance
Access to comprehensive Total Rewards programs (where applicable), including healthcare plans, retirement savings programs, employee assistance initiatives, and stock purchase options, in accordance with company policy
Why Join This Opportunity?
This role offers a unique opportunity to support government-sponsored clinical research at a senior coordination level while contributing to high-impact studies that protect and improve public health. You will work within a globally respected CRO environment that values scientific rigor, regulatory excellence, and professional growth.
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Delhi | India | New Delhi | PAN-India |Assam :
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Hajipur | Patna |Kerala :
Kannur | Kochi | Malappuram | Thiruvananthapuram | Trivandrum |Pondicherry (Puducherry) :
Pondicherry (Puducherry) |Jharkhand :
Ranchi |Sikkim :
Rangpo |India :
Siliguri |Illinois :
Abbott Park | Bloomingdale | Champaign | Chicago | Deerfield | Glenview | Lake Forest | Lombard | Naperville | Norridge | Park RIdge | Round Lake |Maryland :
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Anchorage | Barrow | Bethel | Juneau | Sitka | Wrangell |Massachusetts :
Andover | Billerica | Boston | Cambridge | Devens | Lexington | Massachusetts | Medford and Somerville | Rockland |Wisconsin :
Appleton | Kenosha | Pleasant Prairie | Portage | Waukesha |United states :
Arizona | Buffalo Grove | Clayton | Downers Grove | fairmont | Georgia | Keene | Michigan | Mt. Pleasant | New Jersy | OH | Piedmont | Salisbury | United States | Whitesboro | Winston-Salem |Georgia :
Atlanta | Augusta | Rome |Maine :
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Frank Scottile Blvd |Missouri :
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Berlin |Baden-Wurttemberg :
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Germany | GErmany |Lower Saxony :
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Mitte |Mecklenburg Vorpommern :
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Europe | France | Latvia | Lendava | Leuven | Poland | Slovenia | Spain |Finland :
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Istanbul | Turkey |Norway :
Norway | NOrway |Romania :
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Wavre |Tipperary :
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Dún Laoghaire |Galway :
Galway |County Dublin :
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China | Quarry Bay |Liaoning :
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Hangzhou |Tokiyo :
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Netherlands |Remote Australia :
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Queensland |Melbourne :
South Yarra |United Kingdom :
England | Harlow | Leeds | London | Maidenhead | Salt Lake City | Stevenage | Stirling | United Kingdom |North Yorkshire :
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Australia | North York | Mississauga | Richmond Hill | Uxbridge | Renfrew |Canada :
Canada |Quebec :
Montreal |Brussels :
Brussels |Antwerp :
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Zaventem |South America :
Peru | Argentina |Brazil :
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Athens | Koropi |Greece :
Greece |North Island :
Auckland |New Zealand :
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Barcelona |Madrid :
Madrid |Cebu Province :
Cebu City |Philippines :
Manila |Croatia :
Croatia |Zagreb :
Zagreb |Estonia :
Tartu | Estonia |Harju County (Maakond) :
Tallinn |Hà Nội :
Hà Nội | Hanoi |Ho Chi Minh :
Ho Chi Minh City |Italy :
Italy |Lombardy :
Rho |Jakarta :
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Surabaya |Japan :
Saitama | Japan |Tokyo :
Otemachi |North Ostrobothnia :
Oulu |Southwest Finland (Varsinais-Suomi) :
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Kuala Lumpur |Kyiv Oblast :
Kyiv |Lima Region :
Lima |France :
Lyon | Paris |South Africa :
South Africa | Midrand |Nišava District :
Niš |Bohemia :
Prague |Chile :
Santiago |Bosnia and Herzegovina :
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