Clinical Research Associate II – Full Service (Oncology)
Location: Home-Based, Central US (WV)
Job ID: 25101618
Updated: September 19, 2025
Company Overview
Syneos Health® is a fully integrated biopharmaceutical solutions organization focused on accelerating customer success. Our Clinical Development model centers on the patient and customer while streamlining processes and driving innovation.
Employees: 29,000 across 110 countries
Impact: Involved with 94% of novel FDA-approved drugs, 95% of EMA-authorized products, over 200 studies across 73,000 sites, and 675,000+ trial patients
Culture:
Total Self culture – be your authentic self
Career development, peer recognition, and training
Diversity, equity, inclusion, and belonging
Role Summary
The Clinical Research Associate II (CRA II) monitors clinical research studies, ensuring compliance with Good Clinical Practice (GCP) and regulatory requirements. Responsibilities include on-site and remote monitoring, creating monitoring tools, contributing to SOPs, and managing defined project components.
Impact: Enhances the quality, integrity, and efficiency of clinical trials, directly contributing to reliable study results and improved patient outcomes.
Key Responsibilities
Conduct on-site and remote monitoring of clinical trials
Review study protocols, informed consent forms, and case report forms
Develop and implement monitoring plans, checklists, and templates
Contribute to SOPs, processes, and training materials
Manage project components (site visits, tracking study progress, resolving issues)
Document monitoring activities (reports, follow-up letters, action plans)
Collaborate with cross-functional teams to support trial operations
Qualifications
Education: Bachelor’s degree or equivalent experience in a related field
Experience: 2–4 years in clinical research monitoring
Knowledge: Good Clinical Practice (GCP) guidelines and regulatory requirements
Skills:
Excellent communication and interpersonal abilities
Attention to detail, analytical thinking, and problem-solving
Strong organizational and time management skills
Ability to work independently and manage multiple priorities
Proficiency in Microsoft Office and clinical trial management systems
Certifications:
Certified Clinical Research Associate (CCRA) or equivalent preferred
Benefits
Health coverage: Medical, Dental, Vision
401(k) with company match
Employee Stock Purchase Plan eligibility
Commissions/bonus based on performance
Flexible paid time off (PTO) and sick time
Company car or car allowance (where applicable)
Salary
Base salary range reflects anticipated low and high for this role. Actual salary depends on experience, skills, and qualifications.
Additional Information
Duties may change at company discretion
Equivalent skills and experience may be considered
Compliance with ADA and EU Equality Directive requirements
This posting is not an employment contract
Core Focus Areas
Conduct thorough on-site and remote monitoring of clinical studies
Develop and implement monitoring tools and processes
Manage defined project components
Apply professional knowledge and experience to ensure trial quality
Maintain high standards of clinical practice
Apply / Connect
Apply directly through Syneos Health
Join the Talent Network for updates on new opportunities
Website: www.syneoshealth.com
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Duluth | Eden Prairie | Fridley | Hibbing | Maple Grove | Minneapolis and St. Paul, Minnesota. | Minnetonka | St.Paul |Missouri :
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Galway |Meath :
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China | Quarry Bay |Hubei :
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Hangzhou |Melbourne :
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Sarajevo |Sofia City :
Sofia |Canada :
Canada |Ontario :
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Prague |Republic of Egypt :
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Japan | Saitama |Tokyo :
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Almaty |Remote Korea :
Remote Korea |Republic of Korea :
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Madrid |Sweden :
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