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Clin Ops Specialist - Beijing

0-2 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:

Clinical Operations Specialist – Beijing

Location: Client Site, Beijing, China
Job ID: 25102059
Updated: Yesterday


Company Overview:

Syneos Health® is a fully integrated biopharmaceutical solutions organization focused on accelerating customer success. We translate clinical, medical affairs, and commercial insights into actionable outcomes.

Why Syneos Health:

  • Career development and progression opportunities

  • Supportive and engaged line management

  • Technical and therapeutic area training

  • Peer recognition and total rewards programs

  • Inclusive Total Self culture fostering authenticity and belonging

Vision: Streamline clinical development processes while keeping the patient and customer at the center.


Job Summary:

The Clinical Operations Specialist supports clinical trial operations, site management, and documentation. This role ensures compliance with corporate policies, SOPs, and regulatory requirements while providing support to clinical monitoring staff.

Experience Required: Entry to mid-level; prior clinical research experience preferred.


Key Responsibilities:

1. Clinical Operations & Site Management

  • Perform activities in compliance with Corporate and Clinical Operations Policies, SOPs, and Work Instructions

  • Assist Clinical Monitoring staff with site management activities

  • Serve as Sponsor representative for assigned studies at investigational sites

  • Communicate with sites to ensure protocol compliance and adherence to study procedures

2. Documentation & Trial Master File (TMF) Management

  • Create and maintain TMF and project files, including participation in file audits

  • Prepare and maintain site manuals, reference tools, and other clinical documents

  • Track incoming and outgoing clinical and regulatory documents

  • Maintain clinical tracking information in databases

3. Communication & Coordination

  • Manage shared mailbox and route site requests appropriately

  • Coordinate site supplies, materials, and shipment tracking

  • Assist with team meetings, take meeting minutes, and follow up on action items

4. Data & CRF Handling

  • May handle receipt, tracking, and disposition of Case Report Forms (CRFs) and queries

5. Training & Professional Development

  • Maintain awareness of clinical research developments through completion of assigned training


Qualifications & Skills:

  • Education: High School Diploma or equivalent

  • Skills:

    • Strong communication and interpersonal abilities

    • Willingness to adopt new technologies

    • Minimal travel up to 25% may be required


Additional Information:

  • Job responsibilities are not exhaustive; additional tasks may be assigned

  • Equivalent experience, skills, and education may be considered

  • Compliance with local and international regulations, including ADA provisions

  • This job description does not constitute an employment contract


Application:

  • Apply now or join the Talent Network to stay connected with future opportunities

Learn More: www.syneoshealth.com