Director Clinical Data Management

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  • Melbourne, Victoria
  • Permanent

Director of Clinical Data Management - Leading Clinical Research Consultancy

This company are leading specialists in providing innovative solutions to pharmaceutical, biotechnology, and medical device companies worldwide.With a small team environment and a culture of collaboration, they offer exceptional opportunities for growth and progression.

They are seeking a dynamic and experienced Director of Clinical Data Management to join the team. This pivotal role offers the opportunity for strategic oversight and full management of the global client base. The successful candidate will play a crucial role in driving the success of multiple global clinical research projects and so must have global project lead experience.

Suitable for an experienced Clinical Data Manager with 10 years in the CRO/Pharma industry and at least 5 years project lead experience.

Key Responsibilities:

  • Provide strategic leadership and oversight for the clinical data management team.
  • Manage and mentor a team of clinical data managers, ensuring high performance and professional development.
  • Act as the primary point of contact for our global client base, ensuring exceptional service delivery and building strong, lasting relationships.
  • Collaborate closely with cross-functional teams to ensure seamless project execution and timely delivery of results.
  • Develop and implement best practices and standard operating procedures to optimise data management processes.
  • Ensure compliance with regulatory requirements and industry standards.
  • Drive continuous improvement initiatives to enhance efficiency and quality within the clinical data management function.

Qualifications:

  • Bachelor's degree in life sciences, computer science, or related field; advanced degree preferred.
  • Minimum of 10 years of experience in clinical data management within the pharmaceutical or biotechnology industry.
  • Proven leadership experience, with a track record of successfully managing and developing teams.
  • Strong understanding of clinical trial processes and regulatory requirements (e.g., ICH-GCP, TGA, FDA guidelines).
  • Excellent communication and interpersonal skills, with the ability to effectively interact with clients and internal
  • Proficiency with clinical data management systems and related software.

Why Join:

  • Opportunity to work in a small team environment with a supportive and collaborative culture.
  • Room for progression and advancement within a growing organisation.
  • Chance to make a meaningful impact on the success of clinical research projects worldwide.

If you are a motivated and experienced professional looking for a rewarding opportunity to lead a dynamic team and drive strategic growth in clinical data management, we encourage you to apply.

Please contact Keeley Munday on 02 8310 5854 for more information, or apply direct today.

Keeley Munday Principal Candidate Consultant

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