Global Head of Medical Safety - Belgium, France or Switzerland

Job description

Pleased to meet you, we are Galapagos, a dynamic fast growing Biotech company with offices in Europe in Belgium (Mechelen),  Switzerland (Basel), France (Romainville), the Netherlands (Leiden) and in US, Boston.

 

We’re in the business of changing lives.  In our quest to discover and develop life-improving medicines we go where no one has ever gone before.   In every challenge we face, we see new opportunities.  We want to challenge the impossible.  We need thought leaders and rapid thinkers, entrepreneurs in spirit and status quo-fighters.  Collaborative innovators and perseverant idealists. We need the best-in-class.  In other words, we need you: The ‘make-it-happeners’. 

 

We are looking for a Global Head of Medical Safety.

Scope of the job

The Global Head of Medical Safety will be the responsible strategic leader for the clinical safety and pharmacovigilance activities of Galapagos. You will serve as a member of the GLPG leadership team and function in a global matrix organization interacting with key stakeholders both internally and externally. This is a highly visible role that will interface across all levels and functional areas and will need to partner closely with the clinical development and commercial teams. The exceptional candidate that we seek will have a proactive and innovative approach and a flexible, hands-on nature that works with a high sense of urgency.

 

Your role:

  • You will provide guidance, expertise, and strategic direction on all aspects of clinical safety throughout the life-cycle for multiple products/programs in development
  • You will build and lead a team of safety physicians to support the ongoing evaluation of safety information during clinical development and to provide state-of-the-art proactive risk management. 
  • You will lead active monitoring and continued assessment of safety profile through systematic signal detection and critical review of aggregate safety data and literature during all phases of the life-cycle of a defined portfolio of medicinal products.
  • You will build the post-marketing pharmacovigilance operations for the detection and management of safety signals.  
  • You will guide the clinical development teams regarding all aspects of clinical safety, including trial design, appropriateness of safety endpoints, analysis and interpretation of safety data.
  • You will be the accountable content owner for all safety relevant content or safety relevant documents during clinical development (e.g. DSUR, Development Risk Management Plans, Safety Analysis Plans) and post approval (e.g. PSUR, RMPs, medical expert statements and answers to HAs requests). Be content owner for safety relevant communications such as DHCP letters and company statements.
  • You will serve as the safety expert providing strategic input to key stakeholders in relation to product safety, understand the business strategy for the product and be knowledgeable about the (medical) context of the respective product class. Be subject matter expert for safety relevant discussions with regulatory agencies and other significant external bodies.

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Requirements

Who are you?

  • You have an MD degree combined with minimum 10 years in pharmacovigilance and/or clinical research/clinical safety experience in the pharmaceutical industry.
  • You have strong leadership experience in Drug Safety, Clinical Safety, Pharmacovigilance or Risk Management 
  • You have experience interfacing with regulatory and health agencies on a global basis
  • You have strong communications skills, both written and spoken, ideally with demonstrable experience in medical / scientific writing.
  • You have excellent networking and relationship building skills for successful cooperation with internal and external customers.
  • You have expertise in international regulations governing drug safety. Experience in managing compliance or audits. Working knowledge of relevant FDA, EU, ICH guidelines, initiatives and regulations governing both Safety reporting and processing for clinical trial environments.
  • You have excellent people management and decision making skills.
  • You have strong influencing skills with the ability to quickly earn credibility across other functional areas.

What’s in it for you ?

 You will be part of a fast growing and amazing company.  As ‘make-it-happener’ you will get all the support you need to make your job successful.  At Galapagos we aim to recruit the best people, who stand out among their peers, with integrity and excellent interpersonal and organizational skills. Our employees are the strength behind Galapagos, a highly motivated team, eager to maintain Galapagos’ leading position and achieve breakthroughs in pharmaceutical research. Galapagos offers a competitive remuneration package and a dynamic work environment.

 

We are Galapagos : together we can make it happen…!