Clinical Research Associate II – Full Service (Oncology)
Location: Home-Based, Central US (TN)
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, streamlining processes and driving innovation.
Employees: 29,000 across 110 countries
Impact: Supported 94% of novel FDA-approved drugs, 95% of EMA-authorized products, 200+ studies, 73,000 sites, and 675,000+ trial patients
Culture & Values:
Total Self culture – encouraging authenticity
Career development, training, and peer recognition
Emphasis on diversity, equity, inclusion, and belonging
Role Summary
The CRA II ensures clinical research studies are conducted in accordance with Good Clinical Practice (GCP) and regulatory standards. Responsibilities include on-site and remote monitoring, developing monitoring tools, contributing to SOPs, and managing defined project components.
Impact:
Maintains quality, integrity, and compliance of clinical trials
Supports 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 progress, resolving issues
Maintain accurate documentation: monitoring reports, follow-up letters, action plans
Collaborate with cross-functional teams to support clinical 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) and regulatory requirements
Skills:
Strong communication and interpersonal skills
Attention to detail and analytical thinking
Problem-solving and critical thinking
Organizational and time management abilities
Ability to work independently and manage multiple priorities
Proficiency in Microsoft Office and clinical trial management systems
Preferred Certification:
Certified Clinical Research Associate (CCRA) or equivalent
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 (if applicable)
Salary
Base salary range represents anticipated low and high for this role
Actual salary varies based on qualifications, experience, and proficiency
Additional Information
Duties and responsibilities may change at company discretion
Equivalent skills and experience may be considered
Compliant with ADA and EU Equality Directive requirements
This posting is not an employment contract
Core Focus Areas
Conduct thorough on-site and remote monitoring
Develop and implement tools, processes, and procedures
Manage defined project components
Apply professional knowledge and experience to ensure trial quality
Maintain high clinical standards
Apply / Connect
Apply directly through Syneos Health
Join the Talent Network for updates on future opportunities
Website: www.syneoshealth.com
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