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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 Hybrid 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 (Home-Based, Central US)

Location: USA-MS-Remote
Job ID: 25101618
Updated: September 19, 2025


Company Overview

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization focused on accelerating customer success. We combine clinical, medical affairs, and commercial insights to deliver meaningful outcomes. Our Clinical Development model places the customer and patient at the center, ensuring innovative and streamlined approaches to clinical research.

  • Employees: 29,000+ across 110 countries

  • Impact: Worked with 94% of Novel FDA Approved Drugs and 95% of EMA Authorized Products

  • Mission: Build a diverse and inclusive workplace where employees thrive, contribute, and belong.

Learn more: www.syneoshealth.com


Why Work at Syneos Health

  • Career development, mentorship, and technical/therapeutic training

  • Supportive management and peer recognition programs

  • Inclusive “Total Self” culture

  • Focus on employee well-being and work-life balance


Job Summary

The Clinical Research Associate II (CRA II) at the P21 level is responsible for ensuring clinical research studies are conducted according to widely accepted clinical practices. The role includes both on-site and remote monitoring, developing quality monitoring tools and processes, and contributing to the design and implementation of SOPs, processes, and policies.

Key Contributions:

  • Ensures quality, compliance, and integrity of clinical trials

  • Plays a vital role in advancing medical knowledge and improving patient outcomes

  • Works as an individual contributor in a professional or technical discipline


Key Responsibilities

  1. Monitoring:

    • Conduct on-site and remote monitoring of clinical trials

    • Review study protocols, informed consent forms, and case report forms (CRFs)

  2. Quality Assurance:

    • Develop and implement monitoring tools, procedures, and processes

    • Create monitoring plans, checklists, and templates

  3. Process & Policy Contribution:

    • Assist in development of SOPs, training materials, and programs

    • Participate in process improvement initiatives

  4. Project Management:

    • Coordinate site visits and track study progress

    • Manage defined components of projects within the area of responsibility

  5. Documentation & Reporting:

    • Document monitoring activities and findings accurately and promptly

    • Prepare monitoring reports, follow-up letters, and action plans

  6. Collaboration:

    • Work with investigators, site staff, and cross-functional teams to ensure smooth study conduct


Qualifications

  • Education: Bachelor’s degree in a related field or equivalent experience

  • Experience: 2–4 years in clinical research monitoring

  • Knowledge: Strong understanding of Good Clinical Practice (GCP) and regulatory requirements

  • Skills:

    • Excellent communication and interpersonal skills

    • Strong organizational, time management, analytical, and problem-solving skills

    • Ability to work independently and manage multiple priorities

    • Proficiency in Microsoft Office Suite and clinical trial management systems

Preferred Certification:

  • Certified Clinical Research Associate (CCRA) or equivalent


Key Competencies

  • Attention to detail

  • Critical thinking and problem-solving

  • Team collaboration and adaptability

  • High professional and ethical standards


Benefits

  • Health coverage: Medical, Dental, Vision

  • Company car or car allowance (if applicable)

  • 401(k) match and Employee Stock Purchase Plan

  • Performance-based bonus/commission opportunities

  • Flexible paid time off (PTO) and sick leave

Note: Eligibility for paid sick time varies by state and municipality.


Salary

  • Base salary range reflects anticipated low and high for the position.

  • Actual salary depends on candidate’s experience, skills, competencies, and role proficiency.


Additional Information

  • Tasks and responsibilities may evolve at the company’s discretion

  • Equivalent experience and skills may be considered

  • Not intended to create an employment contract

  • Syneos Health complies with all applicable disability accommodation and employment laws


Core Focus:

  • Conduct thorough on-site and remote monitoring

  • Develop tools, processes, and procedures for quality monitoring

  • Manage project components effectively

  • Maintain high standards of clinical practice and trial success