Senior Clinical Trial Manager (CNS)

Senior Clinical Trial Manager (CNS)

ICON

France/Spain/Portugal/Italy/Romania

This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. Our Clinical Trial Managers act as the Functional Lead from Clinical Operations with responsibility for delivery of all Clinical Operations aspects of clinical studies ensuring consistency with ICON SOPs, study contracts and budgets.

Overview of the role

  • As a Manager, you would be expected to recognize the importance of and create a culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs;
  • Primary point of contact for Clinical Operations aspects of designated projects and responsible for developing successful working relationships with clients;
  • Responsible for planning, scheduling and implementing the Clinical Operations aspects of projects;
  • Contribute to the development and maintenance of cross functional project management plans;
  • Responsible for risk mitigation strategies, associated action plan and issue resolution;
  • Responsible for managing the Clinical Operations project team, including ensuring all necessary project training is provided to assigned staff;
  • Provide direction and support to the Clinical Operations study team;
  • Collaborate with Business Development (BD) to ensure timely completion of change orders;
  • Track Clinical Operations project deliverables using appropriate tools.

Role Requirements

  • University/Bachelor’s Degree in medicine, science or equivalent degree/experience;
  • A satisfactory progression of monitoring experience with previous experience in leadership and/or management activities;
  • Strong CNS background as a CTM is a must;
  • Previous working experience within the clinical trial management field;
  • Thorough knowledge of ICH GCP and relevant regulations for the conduct of clinical trials;
  • Some knowledge of project management processes and tools;
  • Fluent in written and spoken English.

Due to the nature of this position it may be required for the employee to travel approx 25%. Therefore, dependent on the employee’s location, the employee may be required to possess a valid Driver’s license

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