Clinical Project Director

About the Company
• An expanding, global Clinical Research Organisation with presence in over 15 locations worldwide
• Global reputation in creating and executing clinical research in a large range of therapeutic areas
• A unique point of difference – Their profits support their parent organisation which is a not-for-profit medical research institution

About the opportunity
A unique opening has arisen for an experienced Senior Clinical Project Manager/Clinical Project Director with solid Oncology and Leadership background to join a well-known CRO. They are open to all experienced applicants across the APAC Region. You will be working on stimulating projects with regional and/or global teams in a CRO that genuinely has an impact on improving the wellbeing of millions worldwide.

Responsibilities
• Overall management and quality of a group of projects for a particular client, therapeutic area or other speciality area - the role may be local, regional or globally focused depending on the group of projects under responsibility
• Supervising all aspects of project delivery, project quality and financial accountability and managing the Sponsors expectations in all areas
• Providing clear guidance to the project team on project specific deliverables as defined in contracts and project specific documentation
• Managing the implementation, ongoing evaluation, prioritisation, reporting and timely delivery of all operational aspects of allocated projects.

Skills and Experience
• Tertiary qualifications in a related science or health care discipline
• Experience and expertise in clinical trials research – ideally a minimum of 10 years, including Phase I-IV studies and strong Oncology background
• Experience in clinical project management– ideally a minimum of 5 years in a senior project management position
• Line management experience in project management or/or clinical operations is desirable
• Demonstrated expertise in clinical project management and study methodology
• Understanding of academic research is desirable
• Excellent working knowledge of current ICH/GCP, ethical and regulatory requirements
• Experience in managing vendors and suppliers to successful delivery
• Highly developed interpersonal, relationship building, negotiation and conflict resolution skills
• Excellent communication skills including verbal, written, and presentation skills
• Commercial acumen, experience in preparing and tracking budgets
• Proficiency in Microsoft Office packages and clinical trial management software and familiarity with databases
• Demonstrated adaptability and flexibility in view of changing circumstances and priorities

Why this opportunity is right for you
• Competitive remuneration
• Being part of a global team, making a social impact
• Flexible and agile working arrangements with a focus on employee well-being

How to Apply
Click apply or contact Maddy Rhodes–Laird, Senior Recruitment Consultant on 03 9938 7101 for a confidential discussion.