ICON plc
ICON plc
ICON plc is a global contract research organisation serving the healthcare and pharmaceutical industries. Its work spans clinical, consulting, and commercial services that support drug development from early research through post-marketing activities. The company provides solutions including decentralised clinical trials, cardiac safety, early clinical laboratories, medical imaging, regulatory intelligence, and real-world evidence. ICON plc also brings therapeutic expertise to areas such as cardiovascular disease, oncology, internal medicine, cell and gene therapies, and biosimilars, combining data analysis with patient-focused approaches to help advance clinical programmes.

Clinical Site Manager II – Beijing (Hybrid)

Lead site monitoring, compliance, and trial delivery for ICON plc’s sponsor-dedicated clinical research programs in China.

Description

  • Direct clinical trial operations in line with study protocols, regulations, and industry standards
  • Take ownership of technically complex monitoring activities while advancing quality and continuous improvement
  • Verify that study sites follow protocols, regulatory obligations, and Good Clinical Practice (GCP) requirements
  • Visit sites to evaluate performance, address issues, and help keep trials on track
  • Partner with cross-functional teams to support accurate, timely data collection and reporting
  • Train and mentor site personnel and fellow Clinical Research Associates
  • Develop strong working relationships with investigators, site teams, and other stakeholders
  • Coordinate multiple sites and projects concurrently

Requirements

  • Bachelor’s degree in a relevant scientific or healthcare-related discipline
  • Substantial Clinical Research Associate experience, including a strong command of clinical trial processes and regulatory requirements
  • Demonstrated success managing several sites and projects at once, supported by strong organization and problem-solving abilities
  • Advanced knowledge of monitoring methods, data integrity, and site management, plus proficiency with applicable clinical trial software and tools
  • Strong communication, interpersonal, and stakeholder-management capabilities, with the ability to influence compliance in a complex setting
  • Availability to travel as needed, approximately 60% of the time
  • Legal authorization to work in the country where the position is located

Benefits

  • Competitive base pay with performance-based incentives
  • Health and wellbeing programs, including medical, dental, and vision coverage where applicable
  • Retirement and pension benefits
  • Life assurance and disability protection
  • Employee assistance programs and wellbeing resources
  • Professional development through structured training and career progression pathways

Related Jobs

PMA Consultants

NetSuite Project Accounting Specialist

PMA Consultants

Manage NetSuite billing and project financial records for PMA Consultants’ construction consulting work, coordinating with project managers, finance, operations, and clients. Track budgets, invoices, expenses, and payment issues across the project lifecycle.

Open