Clinical Trial Manager

2 months ago

Hong Kong, Central and Western District, Hong Kong SAR China IQVIA Full time

Job Overview

Clinical Trial Managers play a vital role in the delivery of clinical trials, working closely with cross-functional teams to drive project success. As a Clinical Trial Manager at IQVIA, you will be responsible for leading clinical teams and collaborating with project leaders to ensure timely and successful delivery of clinical studies.

Key Responsibilities

  • Ensure clinical delivery of assigned projects in compliance with regulatory requirements, customer needs, and internal standards.
  • Develop and implement recruitment strategies to meet project targets.
  • Contribute to the development of project risk mitigation plans and manage clinical risks throughout the project lifecycle.
  • Ensure clinical quality delivery by identifying quality standards, planning compliance measurement, and monitoring quality issues.
  • Manage clinical aspects of project finances, including Estimate at Completion (EAC), and create plans to deliver.
  • Identify and manage clinical stakeholders, including internal and external stakeholders, through effective communication and resolution management.
  • Collaborate with clinical teams to support milestone achievements and report to internal and external stakeholders as required.
  • Resourcing and talent planning of the clinical team, including managing the clinical team at project level to deliver high-quality operational plans and guidance.
  • Conduct regular team meetings and communicate effectively to achieve objectives.
  • Support professional development by providing feedback to clinical team line managers on performance relative to project tasks.
  • Contribute to the development of clinical delivery strategies for proposals and participate in bid defense preparations and meetings.
  • Mentor and coach new peers as they assimilate into this role.
  • Work as a primary Clinical Lead alongside other Clinical Leads to deliver large, global trials.

Requirements

  • Bachelor's Degree in a healthcare or scientific discipline.
  • 5 years of clinical research/monitoring experience or equivalent combination of education, training, and experience.
  • Basic knowledge of project management practices and terminology.
  • Good knowledge of applicable clinical research regulatory requirements, including Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
  • Broad protocol knowledge and therapeutic knowledge.
  • Good understanding of the clinical research industry and relevant environments.
  • Understanding of project finances.
  • Knowledge of clinical trials, including clinical trial conduct and applicable regulatory requirements.
  • Strong written and verbal communication skills, including good command of the English language.
  • Problem-solving skills.
  • Planning, time management, and prioritization skills.
  • Ability to handle conflicting priorities.
  • Attention to detail and accuracy in work.
  • Results-oriented approach to work delivery and output.
  • Good influencing and negotiation skills.
  • Effective mentoring and training skills.
  • Good software and computer skills, including Microsoft Office applications.
  • Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
  • Ability to work across geographies, displaying high awareness and understanding of cultural differences.
  • Ability to influence without authority.

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