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

2-4 years
Not Disclosed
10 Sept. 25, 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

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

  1. Thorough on-site and remote monitoring of clinical studies

  2. Develop and implement monitoring tools and processes

  3. Manage defined project components

  4. Apply professional knowledge and skills to ensure trial quality

  5. 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