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Cra I - Beijing

2-4 years
Not Disclosed
10 Oct. 10, 2025
Job Description
Job Type: Full Time 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:

CRA I (Clinical Research Associate I)

Location:

Beijing, China – Client Site

Job ID:

25102057


Company Overview:

Syneos Health® is a fully integrated biopharmaceutical solutions organization that accelerates customer success by translating clinical, medical affairs, and commercial insights into outcomes.

Highlights:

  • Patient- and customer-centric clinical development model

  • Agile, innovative team environment

  • 29,000 employees across 110 countries

  • Inclusive Total Self culture fostering authenticity and belonging


Job Summary:

The CRA I conducts on-site and remote monitoring of clinical research studies to ensure compliance with GCP and regulatory standards. This role develops monitoring tools, tracks study progress, and contributes to the implementation of processes and policies to ensure high-quality trial conduct.


Key Responsibilities:

  • Conduct on-site and remote monitoring of clinical studies

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

  • Develop and implement monitoring tools, procedures, and processes (e.g., monitoring plans, checklists, templates)

  • Participate in the design, implementation, and delivery of SOPs, processes, and training materials

  • Manage defined project components, including site visits, study tracking, and issue resolution

  • Document monitoring activities accurately (monitoring reports, follow-up letters, action plans)

  • Collaborate with investigators, site staff, and cross-functional teams to ensure smooth study execution


Qualifications:

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

  • 2–4 years of clinical research monitoring experience

  • Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements

  • Excellent communication and interpersonal skills

  • Ability to work independently and manage multiple priorities

  • Proficiency in clinical trial management systems and relevant software

Preferred Certifications:

  • Certified Clinical Research Associate (CCRA) or equivalent


Necessary Skills:

  • Attention to detail and strong analytical skills

  • Problem-solving and critical thinking

  • Team collaboration skills

  • Strong organizational and time management skills

  • Proficiency in Microsoft Office Suite


Impact and Contribution:

  • Ensures adherence to clinical practices and regulatory requirements, contributing to the quality and integrity of studies

  • Supports the development of monitoring tools and procedures to enhance trial efficiency

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


Job Category:

Clinical Operations / Clinical Monitoring / CRA