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LK is growing and looking to bring onboard additional Clinical Project Managers to join our Clinical Project Management team. Clinical Project Management resides in the Clinical Operations Strategy area that is responsible for driving forward ALK’s global clinical project portfolio.
The ideal candidate for the role will bring professional competencies and experience within clinical project management and can drive clinical projects from idea to reporting, supporting the process of getting new innovative treatments to the market, ultimately improving quality of life for the millions of people suffering from allergies all over the world.
As a Clinical Project Manager at ALK you will be leading the cross functional clinical trial team, ensuring that clinical projects are planned, executed and completed in accordance with the agreed timelines and budget. You will use your understanding of clinical drug development to oversee and report progress, identify risks, and drive mitigations for the trial(s) under your responsibility. In addition, you will drive cross functional optimisation projects.

Your primary tasks will be:

• Leading the clinical trial team from protocol development to reporting of the clinical trial
• Translating science into operational feasible solutions for development, conduct and close-out of clinical trials.
• Collaborate with vendors and ensure oversight and compliance of clinical trial activities
• Drive the clinical part of regulatory submissions, including responses to Health Authorities/Ethical Committees/Institutional Review Boards
• Communicate progress and risks to management.
• Promote knowledge sharing across trials and functions to ensure alignment and optimisation of processes.

• Leading the clinical trial team from protocol development to reporting of the clinical trial
• Translating science into operational feasible solutions for development, conduct and close-out of clinical trials.
• Collaborate with vendors and ensure oversight and compliance of clinical trial activities
• Drive the clinical part of regulatory submissions, including responses to Health Authorities/Ethical Committees/Institutional Review Boards
• Communicate progress and risks to management.
• Promote knowledge sharing across trials and functions to ensure alignment and optimisation of processes