Clinical Trial Manager

4 weeks ago

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

Job Overview

Clinical Leads play a crucial role in the delivery of clinical trials, working closely with clinical teams to bring new treatments to market faster. As a Clinical Lead, you will be part of the core project team responsible for ensuring clinical delivery meets contractual requirements and adheres to Standard Operating Procedures (SOPs), policies, and practices.

Key Responsibilities

  • Ensure clinical delivery of assigned projects in compliance with regulatory requirements, customer needs, and internal standards.
  • Lead clinical teams and collaborate with Project Leaders and other functional teams to ensure projects meet delivery requirements.
  • 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 overseeing quality issues.
  • Manage clinical aspects of project finances, including Estimate at Completion (EAC), and create plans to deliver.
  • Identify and manage clinical stakeholders, communicate effectively, and resolve issues.
  • Collaborate with the clinical team to support milestone achievements and report to internal and external stakeholders.
  • Resourcing and Talent Planning of the clinical team, manage the clinical team at project level, and establish operational plans.
  • Conduct regular team meetings, communicate effectively, and achieve objectives.
  • Support professional development by providing feedback to clinical team line managers.

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, such as 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 applicable regulatory requirements and relevant local laws, regulations, and guidelines.
  • 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.
  • Good influencing and negotiation skills, good judgment, and decision-making skills.
  • Effective mentoring and training skills, fostering learning and knowledge sharing with colleagues.
  • 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.

About IQVIA

IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world.

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