Associate Clinical Lead

IQVIA Inc

Guangzhou, China
On-site
Ensure clinical delivery compliance
Manage project recruitment targets
Develop risk mitigation plans
IQVIA Inc is seeking an Associate Clinical Lead in Guangzhou, China, responsible for ensuring the clinical delivery of assigned projects while meeting regulatory and customer requirements. The ideal candidate will have a background in clinical research, strong communication skills, and a collaborative approach to managing clinical teams

Job Summary

  • Ensure clinical delivery of assigned projects in compliance with regulatory requirements, customer requirements, and internal requirements.
  • Manage clinical aspects of Project Finances including Estimate at Completion (EAC) and identify additional service opportunities or out of scope work.
  • Manage the clinical team at project level to successfully deliver the project through the establishment of high-quality operational plans and guidance and project related trainings.

Matching Summary

Match Score: 85

IQVIA Inc is seeking an Associate Clinical Lead in Guangzhou, China, responsible for ensuring the clinical delivery of assigned projects while meeting regulatory and customer requirements. The ideal candidate will have a background in clinical research, strong communication skills, and a collaborative approach to managing clinical teams.

Skills & Requirements

Must-have

  • Ensure clinical delivery compliance
  • Manage project recruitment targets
  • Develop risk mitigation plans
  • Ensure clinical quality delivery
  • Manage clinical project finances
  • Manage clinical stakeholders
  • Collaborate with clinical team
  • Resourcing and talent planning
  • Conduct team meetings
  • Provide performance feedback

Nice-to-have

  • Influence without authority
  • Work across cultures and geographies
  • Demonstrate IQVIA competencies

Key Requirements

  • 3 years clinical research/monitoring experience
  • Bachelor's Degree in health care or scientific discipline
  • Knowledge of GCP and ICH guidelines
  • Broad protocol and therapeutic knowledge
  • Understanding of Clinical Research industry
  • Basic understanding of project finances
  • Good command of English language
  • Problem solving skills
  • Planning, time management, and prioritization skills
  • Attention to detail and accuracy
  • Good software and computer skills
  • Ability to establish and maintain effective working relationships

Work Rights

Not specified

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