Clinical Research Associate II – Full Service (Oncology)
Location: Home-Based, Central US (IA)
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 places the customer and patient at the center of all we do. We aim to simplify processes, innovate collaboratively, and accelerate the delivery of therapies.
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
Diversity, equity, inclusion, and belonging
Career development, technical training, and peer recognition
Role Summary
The Clinical Research Associate II (CRA II) monitors clinical research studies to ensure compliance with Good Clinical Practice (GCP) and regulatory requirements. This includes both on-site and remote monitoring, development of monitoring tools, and contributing to SOPs, processes, and project components.
Impact: Ensures reliability, integrity, and quality of clinical trials, contributing to improved patient outcomes and medical knowledge.
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 tools, checklists, and templates
Contribute to design and implementation of SOPs, processes, and training materials
Manage project components such as site visits, study tracking, and issue resolution
Document monitoring activities, including reports, follow-up letters, and action plans
Collaborate with cross-functional teams and site staff for smooth trial conduct
Qualifications
Education: Bachelor’s degree in a related field or equivalent experience
Experience: 2–4 years in clinical research monitoring
Knowledge: GCP guidelines and regulatory requirements
Skills:
Excellent communication and interpersonal abilities
Attention to detail, analytical, problem-solving, critical thinking
Organizational and time management skills
Ability to work independently and handle 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 low and high estimates based on qualifications, skills, and experience
Additional Information
Tasks, duties, and responsibilities are not exhaustive; may change at company discretion
Equivalent experience and skills may be considered
Not an employment contract
Compliance with ADA and EU Equality Directive requirements
Core Focus Areas
Thorough on-site and remote monitoring of clinical studies
Develop and implement monitoring tools and processes
Manage defined project components
Apply professional knowledge and skills to ensure trial quality
Maintain high standards of clinical practice
Apply / Connect
Apply for this position directly through Syneos Health
Join the Talent Network to stay connected to other opportunities
Website: www.syneoshealth.com
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