Clinical PM

For one of our clients located in Wallonia, we are looking for a Clinical PM with a previous expertise in Start-up activities and Oncology.

  • Do you have a first expertise within the pharmaceutical industry and the clinical project management?
  • Are you familiar with the Clinical start-up activities?
  • Are you fluent in English?

Then, you might be the specialist that we are looking for!

For one of our clients located in Wallonia, we are looking for a Clinical PM with a previous expertise in Start-up activities and Oncology.

  • Do you have a first expertise within the pharmaceutical industry and the clinical project management?
  • Are you familiar with the Clinical start-up activities?
  • Are you fluent in English?

Then, you might be the specialist that we are looking for!

Responsibilities 
  • Manage activities related to the clinical studies process from protocol summary, study site selection and regulatory activation process to Clinical Study Report

  • Select and activate global study sites, establish and maintain an excellent relationship with site investigators and research teams

  • Create and update project plan on a regular basis to assure appropriate outcome of clinical trial projects in terms of scope, timelines and objectives.

  • Ensure study quality/GCP compliance to deliver a rigorous patient data package

  • Partner and provide oversight to the responsible CRO or study delivery team, ensuring timely delivery of milestones and within budget

  • Propose and implement study process improvements

  • Liaise with manufacturing, central lab, and other study project stakeholders as needed

Profile 
  • At least 7 years’ experience in Clinical development in Biopharma industry (sponsor and/or CRO)

  • 2-4 years’ experience in Clinical Operations/Project management in oncology, prior small start-up company experience in biotechnology is a plus
  • Strong knowledge of ICH and GCP rules and of the complete clinical trials process

  • Thriving in challenging environments and finds ways to remove obstacles to complete enrollment and deliver a robust patient data package

  • Flexible mindset capable to manage change and deal with ambiguity.

  • Proven ability to manage complex projects. Flexibility to re-prioritize workload to meet changing timelines, adaptability.

  • Excellent communicator able to raise the profile of clinical studies within sites and create advocates for recruitment.

  • Autonomous, pro-active personality. Driven to achieving highest results in shortest timeframe.

  • Efficient in planning and executing work

  • Team player, able to manage matrix organization in multi-cultural environment.

  • Good negotiator: direct, forceful and diplomatic.

  • ability to travel up to 30% within US and internationally.

Contact Information 

Interested? Don’t hesitate to contact Lindsay Bousmanne – Talent Acquisition at Valesta

Phone: 02 588 16 01 – Lindsay.bousmanne@valesta.com             

 

 

Application form : Clinical PM

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