Global Clinical Trial Manager

Job details
Posting date: 11 November 2019
Salary: £60,000.00 to £75,000.00 per year
Additional salary information: Car allowance, Bonus, Pension
Hours: Full time
Closing date: 11 December 2019
Location: Uxbridge, London, UB8 1DH
Company: Hays Specialist Recruitment
Job type: Permanent
Job reference: 3694493_1573474141

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Global Clinical Trial Manager, CTM, CPM, CSM, Oncology, Adaptive Trial Design

Your new company

This global Biotech are looking for the right dynamic and organised person to fit in as a Global Clinical Trial Manager as part of their Global Clinical Program Management function. This is a unique opportunity to work in a fast paced, collaborative and highly innovative environment to help ensure a whole new class of novel molecules become medicines. They need the best and brightest to maintain their long term commitment to helping patients and improving health outcomes - putting you in good company.

Your new role

This highly rewarding position will put you at the forefront drug development, with every day different to the last. You will be reporting directly to the Programme and Resource Management, Senior Manager and project oversight will be performed by the Clinical Program Manager. The role will put you in charge of the cross-functional Clinical Study Team; ensuring the budget, quality and time schedule of the original and exciting Clinical Trial Portfolio are in accordance with standards. You will need to have had Global Clinical Project Study Management experience within a CRO, Pharma or Biotech company and experience of such within Oncology is preferable (as is experience in Adaptive Trial Design).

What you'll need to succeed

Main Responsibilities

  • Managing the conduct of clinical trials from study design to close out at global level
  • Leading the Clinical Study Team as well as close collaboration and oversight of cross functional stakeholders
  • Identifying opportunities and risk in order to ensure on budget and on time execution of clinical trial deliverables
  • Ensure adherence to SOPs, regulations and ICH-GCP including Trial Master File management
  • Effective management of vendors to the required standards

What you'll get in return

This exciting role is not only an opportunity to work for one of the leaders in the market but will also put you at the forefront of delivering Clinical Trial Portfolios that will change lives. Your day to day experience will be diverse and rewarding and you will lead a team who shares your ambition and goals.

What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.

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