[Global Role] Clinical Study Lead

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About The Client

Our client is a global biotech company developing cell-targeting therapies using an unique technology, with the goal to broaden the scope in cancer treatments.

The company provides great talent development opportunities for people who are eager to build a career in a fast-paced environment.

Role’s Responsibilities

• Leader of 1-3 studies through clinical studies activities that meet ICH/GCP/SOP requirements.
• Manage clinical studies from planning to closure including goal-setting, timeline, and budget.
• Oversee the performance of study team members in either a matrix management model or as direct reports.
• Manage study-related vendors including CROs and contract labs.
• Responsible for ensuring development and implementation of applicable study plans, e.g., protocols/amendments, informed consent templates, Communication/Risk Mitigation Plan, eCRF & CRF forms/completion guidelines and site reference manuals/instructions.
  
  

Qualifications

• 7+ years of clinical trial management experience in wither CRO or other biotech/pharmaceutical companies.
• Hands-on knowledge and experience in global clinical studies in oncology and managing study timelines, vendor contracts and budgets.
• Strong leadership and project management skills and proven ability to multitask.
• Excellent communication skills in English.
• A team player with the ability to work independently.
• Willingness to travel (both locally and globally) depending on the studies activities.