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Clinical Research Associate Ii - Full Service - Oncology (Home-Based In Central Us)

2-4 years
Not Disclosed
10 Sept. 24, 2025
Job Description
Job Type: Full Time Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

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