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

Syneos Health

2-4 years

Not Disclosed

Remote, USA

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

Job Title:

Clinical Research Associate II / Sr CRA – Full Service (Oncology + General Medicine)

📍 Location: USA-ID-Remote (Home-Based, Western US)
🆔 Job ID: 25101606
📅 Updated: September 25, 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 impactful outcomes addressing modern healthcare realities.

Our Clinical Development Model places both the customer and the patient at the center of all operations. We continuously simplify and streamline processes — making Syneos Health easier to work with and work for.

💡 “Work Here Matters Everywhere.”
Join 29,000 employees across 110 countries, all driven by passion, innovation, and impact.

Why Join Syneos Health

🌱 Career Development & Progression: Continuous learning, advancement opportunities, and technical training.
🤝 Supportive Leadership: Engaged line management and peer recognition.
🎯 Inclusive Culture: Total Self Culture — an environment where you can authentically be yourself.
🌍 Diversity & Belonging: We celebrate diversity of thoughts, backgrounds, and perspectives.
🏆 Rewards & Benefits: Total rewards program, performance bonuses, and flexible work options.

Key Responsibilities

Conduct on-site and remote monitoring of clinical research studies.
Review study protocols, informed consent forms, and case report forms (CRFs) for compliance with Good Clinical Practice (GCP).
Develop and implement monitoring tools, plans, and checklists to ensure data quality.
Contribute to SOP development, training materials, and continuous process improvement.
Manage assigned components of projects (e.g., site visits, issue resolution, progress tracking).
Document monitoring activities — including reports, follow-up letters, and action plans.
Collaborate with investigators, site staff, and cross-functional teams to ensure smooth trial operations.

Qualifications

🎓 Education: Bachelor’s degree in a related field or equivalent experience.
💼 Experience: Minimum 2–4 years in clinical research monitoring.
📘 Knowledge: Strong understanding of GCP and regulatory requirements.
💬 Skills: Excellent communication, interpersonal, and organizational skills.
💻 Technical: Proficiency in Clinical Trial Management Systems (CTMS) and Microsoft Office Suite.

Preferred Certifications

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

Core Competencies

🔍 Attention to detail & analytical mindset.
💡 Problem-solving & critical thinking.
👥 Effective teamwork and collaboration.
⏰ Strong time management & multitasking abilities.
💻 Proficient with Microsoft Office (Word, Excel, PowerPoint).

Compensation & Benefits

💰 Base Salary: Range varies based on skills, experience, and proficiency.
🚗 Perks: Company car or allowance.
🩺 Health Coverage: Medical, Dental, and Vision.
💸 Retirement: Company match 401(k).
📈 Equity: Employee Stock Purchase Plan eligibility.
🎁 Incentives: Bonus/commission opportunities.
🕒 Time Off: Flexible PTO and paid sick leave (in compliance with state/municipal laws).

About Syneos Health (At a Glance)

Partnered with 94% of all Novel FDA Approved Drugs (past 5 years).
Supported 95% of EMA Authorized Products.
Managed 200+ Studies, 73,000 Sites, and 675,000+ Trial Patients.

“No matter your role, challenge the status quo with us.”
🌐 Learn more: www.syneoshealth.com

Additional Information

Duties and responsibilities may evolve.
Equivalent education or experience may be considered.
Syneos Health complies with ADA and EU Equality Directive for equal employment opportunities.
Reasonable accommodations are provided when necessary.

Role Summary

Position Level: P21
Roles at this level ensure clinical studies are conducted per established clinical practices and protocols, contributing directly to study integrity and quality.

Core Focus Areas:

Conduct comprehensive on-site and remote monitoring.
Design & implement monitoring tools and procedures.
Manage defined project components independently.
Maintain high standards of clinical practice.
Advance study efficiency and data reliability.

Impact:
Your work ensures clinical trial integrity, efficiency, and reliability, ultimately advancing medical knowledge and improving patient outcomes.

How to Apply

🔗 Apply Now or
💡 Join our Talent Network to stay connected for future opportunities.

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Diversity Statement

Syneos Health is committed to creating a diverse, inclusive, and authentic workplace.
If your experience doesn’t align perfectly, apply anyway — we value transferable skills and potential.

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

Job Description

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