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Senior/Clinical Trial Manager

3 months ago


Brisbane, Queensland, Australia Pharmiweb Full time

At ICON, the exceptional people on our teams set us apart. Our diversity enables us to better serve our customers and fulfill our mission to enhance patients' lives.

Our unique 'Own It' culture is guided by four core values that unite us as individuals and distinguish us as an organization: Accountability & Delivery, Collaboration, Partnership, and Integrity. We strive to be the premier Clinical Research Organization that provides top-notch service to our clients and patients at every interaction. In essence, we aim to be the preferred partner in drug development.

This is our vision. We are passionate about it. And we are looking for talented individuals who share this vision.

If you are as motivated as we are, consider joining us. You will be part of a vibrant and supportive atmosphere, surrounded by some of the brightest and most amiable professionals in the industry, contributing to the advancement of an entire sector.


Job Title: Clinical Trial Manager - CNS and Rare Diseases

Company: ICON

Locations: Georgia, Poland, Bulgaria, South Africa, Ireland, Spain, UK, Romania, Latvia, Lithuania, Hungary, Serbia, Portugal, Slovakia, Slovenia

Responsibilities:
  • Lead clinical aspects of assigned projects, ensuring adherence to budget and timelines.
  • Serve as the primary point of contact for clinical aspects of assigned projects and build successful cross-functional relationships with internal and external stakeholders.
  • Initiate process improvement efforts to boost efficiency and value.
  • Supervise clinical metrics and ensure compliance with quality standards.
  • Manage the clinical project team to enhance performance and productivity.
  • Participate in clinical risk assessment and resolution.
  • Maintain the Trial Master File and ensure compliance with Standard Operating Procedures.
  • Engage in recruitment and business development activities.
  • Occasional domestic and international travel required (about 25%).

Qualifications:
  • Bachelor's degree in a related field (advanced degree preferred).
  • Years of experience in clinical project management.
  • Excellent communication and leadership capabilities.
  • Able to manage multiple priorities in a fast-paced setting.
  • Familiarity with clinical trial processes and regulations.
Benefits of Working at ICON:
Our success is driven by the caliber of our team. That's why we prioritize creating a culture that recognizes high performance and fosters talent.

We offer competitive salary packages, regularly benchmarked against industry standards. Our annual bonuses are tied to achieving performance objectives - for both our team and you.

We also provide a variety of health benefits for employees and their families, along with robust retirement plans and additional perks like life insurance, ensuring you can save for the future with confidence.

Yet beyond the attractive salaries and comprehensive benefits, you will thrive in an environment that encourages you to fulfill your purpose and make a lasting impact.


ICON is an equal opportunity employer dedicated to fostering a workplace free from discrimination and harassment. All qualified candidates will receive fair consideration for employment, regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

If you require a reasonable accommodation due to a medical condition or disability during any part of the application process or while performing the essential job functions, please inform us through the provided channel.