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Global Trial Manager

  1. Any EMEA Location
2023-106899
  1. ICON Strategic Solutions
  2. Clinical Trial Management
  3. Remote

About the role

This vacancy has now expired. Please click here to view live vacancies.

As a Global Trial Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.


What you will be doing:

  • Act as primary company contact for assigned trial at the country level and ensure local/country team is tracking project progress against planned timelines and monitors patient recruitment rate to ensure that target enrollment will be met across the allocated countries
  • Act as primary company contact for assigned trial at the country level and ensure local/country team is tracking project progress against planned timelines and monitors patient recruitment rate to ensure that target enrollment will be met across the allocated countries
  • In coordination with the Functional Manager/ GPL, Study Responsible Scientist/Physician (SRS/SRP) and/or Clinical Leader, provide adequate project-specific training to the CRO/ GCO teams and to the site staff.
  • Work with CRO/ GCO staff in the set-up and coordination of Investigator Meetings, if applicable
  • Lead the Study Management Team (SMT) in assigned country/ countries.
  • Contribute to country/site level recruitment strategy and contingency planning and implementation in partnership with other functional areas to achieve recruitment target.
  • Deliver competent vendor management at the country level to support the study and may submit requests for vendor services and support vendor selection
  • Drive study compliance by maintaining and updating trial management systems, using study tools and management reports available to analyze study progress
  • Engage with country MAF teams on study/ program progress and issue escalation, as applicable, during planning, execution and close-out.
  • Autonomy with execution of local trial management services.
  • Depth of knowledge with local trial management services.
  •  

You are:

 

  • BA/BS degree.
  • Degree in a health or science related field.
  • Minimum of 5 years of clinical research experience in the pharmaceutical industry or CRO.
  • Specific therapeutic area experience may be required depending on the position.
  • Strong working knowledge of ICH-GCP, company standard operating procedures, local laws and regulations, assigned protocols and associated protocol specific procedures.
  • Strong IT skills in appropriate software and company systems. A willingness to travel with occasional overnight stay away from home according to business needs.
  • Excellent decision-making and string financial management skills.
  • Proficient in speaking and writing the country language and English. Good written and oral communication skills as appropriate.
  • Flexibility and ability to manage study teams in a virtual environment
  •  


Why ICON?

Our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.

ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

 

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