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Clinical Research Associate Ii / Sr Cra - Full Service - Onc + Gen Med (Home-Based In Western Us)

0-2 years
Not Disclosed
10 Oct. 2, 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 / Sr CRA (Full Service - Oncology + General Medicine)

Location: USA-CA-Remote (Home-Based in Western US)
Updated: September 25, 2025
Job ID: 25101606


🌍 About Syneos Health

Syneos Health® is a fully integrated biopharmaceutical solutions organization dedicated to accelerating customer success. We translate clinical, medical affairs, and commercial insights into impactful outcomes, addressing modern healthcare realities.

Our Clinical Development model keeps both customers and patients at the center of all activities. We focus on simplifying and streamlining operations to make Syneos Health easier to work with—and easier to work for.

With 29,000 employees across 110 countries, Syneos Health believes:

WORK HERE MATTERS EVERYWHERE.


💡 Why Join Syneos Health

  • 🚀 Career Growth: Development programs, technical and therapeutic training, and clear progression paths.

  • 🤝 Supportive Management: Engaged leadership with mentorship opportunities.

  • 🏆 Recognition & Rewards: Peer recognition and total rewards program.

  • 🌈 Inclusive Culture: Our Total Self culture allows everyone to be authentic, fostering diversity and belonging.


🎯 Key Responsibilities

  • Conduct on-site and remote monitoring to ensure study compliance with protocols, GCP, and regulatory standards.

  • Review study documents such as protocols, informed consent forms, and case report forms (CRFs).

  • Develop and implement monitoring tools, checklists, and plans to maintain study quality.

  • Contribute to SOPs, training materials, and continuous process improvement.

  • Manage site visits, study tracking, and issue resolution within assigned projects.

  • Document findings through monitoring reports, follow-up letters, and action plans.

  • Collaborate with investigators, site staff, and cross-functional teams for smooth trial operations.


🎓 Qualifications

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

  • Experience: 2–4 years in clinical research monitoring.

  • Knowledge: Strong understanding of ICH-GCP guidelines and global regulatory requirements.

  • Technical Skills: Proficiency in CTMS and related systems.

  • Soft Skills: Excellent communication, organization, and multitasking abilities.


🧾 Preferred Certifications

  • Certified Clinical Research Associate (CCRA) or equivalent certification preferred.


🧠 Core Skills

  • Attention to detail and strong analytical ability.

  • Problem-solving and critical thinking.

  • Team collaboration and independence.

  • Time management and prioritization.

  • Proficiency in Microsoft Office Suite.


💼 Compensation & Benefits

Syneos Health offers a comprehensive benefits package including:

  • Company car or car allowance.

  • Health benefits: Medical, Dental, and Vision.

  • Retirement: 401(k) with company match.

  • Stock Options: Employee Stock Purchase Plan.

  • Performance Incentives: Bonus/Commission eligibility.

  • Work-Life Balance: Flexible PTO and regulated sick time.

💰 Salary Range: Based on candidate qualifications, skills, and proficiency.


🌎 About Syneos Health’s Impact

  • Collaborated on 94% of Novel FDA-approved drugs and 95% of EMA-authorized products in the last 5 years.

  • Supported 200+ studies across 73,000+ sites with 675,000+ trial patients.

Learn more at 🔗 syneoshealth.com


⚙️ Additional Information

  • Responsibilities may be adjusted as needed.

  • Equivalent experience, skills, or education may substitute formal requirements.

  • Syneos Health is ADA compliant and provides reasonable accommodations when needed.

  • Fully aligned with EU Equality Directive and non-discrimination policies.


🧭 Role Summary

Job Family: Clinical Monitoring / CRA (P21 Level)
Function:

  • Conduct on-site and remote monitoring.

  • Develop and implement monitoring tools and processes.

  • Manage assigned project components.

  • Contribute to high-quality clinical data and compliance.

Impact:
Ensures the integrity and reliability of clinical research studies, directly supporting advancements in medical knowledge and patient care.


🚀 Core Focus Areas

  • ✅ On-site and remote monitoring excellence.

  • 🧩 Tool and process development for quality assurance.

  • 📈 Project component management.

  • 🎓 Practical application of professional knowledge and experience.


📩 Apply Now

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