Job Title:
Clinical Research Associate II – Full Service – Oncology
Company: Syneos Health®
Location: USA-MI (Home-Based, Central US)
Job ID: 25101618
Updated: September 19, 2025
About Syneos Health
Syneos Health® is a fully integrated biopharmaceutical solutions organization that accelerates customer success. Our Clinical Development model centers on patients and customers, continuously simplifying and streamlining processes to improve outcomes.
Key Highlights:
29,000 employees across 110 countries
Supported 94% of Novel FDA Approved Drugs, 95% of EMA Authorized Products
Contributed to 200+ studies across 73,000 sites and 675,000+ trial patients
Culture & Values:
Total Self culture – encouraging authenticity and inclusivity
Career development, training, recognition, and total rewards
Collaborative, innovative, and supportive environment
Job Summary
The CRA II – Full Service (Oncology) role is responsible for monitoring clinical research studies, ensuring adherence to clinical practices, regulatory requirements, and study protocols. This role is primarily home-based in the Central US and involves both on-site and remote monitoring.
Core Responsibilities
Conduct on-site and remote monitoring of clinical studies, reviewing study protocols, informed consent forms, and case report forms.
Develop and implement monitoring tools, procedures, and processes, including monitoring plans, checklists, and templates.
Contribute to the design, implementation, and delivery of processes, programs, and policies, including SOPs and training materials.
Manage defined project components, such as coordinating site visits, tracking study progress, and resolving issues.
Document monitoring activities accurately and timely, including monitoring reports, follow-up letters, and action plans.
Collaborate with cross-functional teams, including investigators and site staff, to ensure smooth study conduct.
Qualifications
Bachelor’s degree in a relevant field or equivalent experience
2–4 years of experience in clinical research monitoring
Strong knowledge of Good Clinical Practice (GCP) and regulatory requirements
Excellent communication and interpersonal skills
Ability to work independently and manage multiple priorities
Proficiency with clinical trial management systems and relevant software
Certifications:
Certified Clinical Research Associate (CCRA) or equivalent preferred
Necessary Skills:
Attention to detail and strong analytical skills
Critical thinking and problem-solving abilities
Ability to work effectively in a team environment
Strong organizational and time management skills
Proficiency in Microsoft Office Suite
Benefits & Compensation
Company car or car allowance (if applicable)
Health benefits: Medical, Dental, Vision
401(k) plan with company match
Employee Stock Purchase Plan eligibility
Commissions/bonus opportunities based on performance
Flexible PTO and sick time (subject to local regulations)
Salary:
Base salary depends on qualifications, skills, and experience
Additional Information
Tasks and responsibilities may evolve based on business needs
Equivalent experience, skills, and education may be considered
Syneos Health is committed to diversity, equity, inclusion, and compliance with the Americans with Disabilities Act (ADA)
Summary of Role Impact
Ensures clinical research studies are conducted per accepted practices
Develops and implements monitoring tools and procedures to enhance trial quality
Contributes to the reliability and validity of study results
Plays a key role in advancing medical knowledge and patient outcomes
How to Apply
Join the Syneos Health Talent Network to be considered for this role:
Syneos Health Careers
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