Clinical Site Manager

il y a 2 semaines


Bruxelles, Région de Bruxelles, Belgique Hobson Prior Temps plein

Hobson Prior are currently seeking for a Clinical Site Manager to join a fantastic pharmaceutical establishment on a contract basis located in Brussels.

Our client is focused on producing valuable solutions to improve the lives of many.

Please note that to be considered for this role you must have the right to work in this location.

Key Responsibilities:

  • For this position, you will be accountable for the early engagement with KOLs/sites/patient organisations and main point of contact for these throughout the study.
  • Responsible for attending crucial therapeutic training/meetings and/or industry training.
  • You will develop, discuss and implement site engagement method/plan in collaboration with the company's clinical team and crucial internal shareholders throughout the lifecycle of the company's clinical trials.
  • Serve as the main point of contact for sites concerning studyconnected problems.
  • Assist the CMP in management of the study, which may involve vendor management training logistics, etc.
  • Any other assigned duties.

Key Skills:

  • Able to analyse, synthesis and clearly display information to a varied audiences with the capacity to resolve issues.
  • Solid facilitation abilities with the capacity to work well with others.
  • Presentation and communication skills both verbally and in writing.
  • Works well in a global and swiftly changing setting.
  • Able to oversee supervising and linked actions within clinical trials.
  • A curious and agile individual with a nothing is impossible mindset.
  • Capable of having scientific conversations with both investigators and site staff.
  • Works well under mínimal supervision as well as under pressure.

Requirements:

  • Educated to a degree level. An advanced degree level would be ideal.
  • At least 5 years of experience working within a pharmaceutical, biotech and/or Cro establishment with experience in a site management or investigator facing role.
  • At least 3 years of experience supervising trials in a clinical development setting, ideally within phase II
  • IV.
  • Expertise on GCP and ICH regulations.
  • Fluency in the English language with knowledge in any other language would be advantageous.
  • Computer literacy.
  • Willing to travel for business needs up to 50% of the time.


Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe.

Hobson Prior is acting as an Employment Agency in relation to this vacancy.

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