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575 offres d'emploi Associate Director Director, Regulatory - Flanders


Associate Director in Solid State Sciences & Characterization

Lieu : Beerse Flanders
Société : Johnson and Johnson

In Belgium (Beerse) there is a vacancy for an Associate Director in Solid State Sciences & Characterization ...

Postuler


Associate Director in Solid State Sciences & Characterization

Lieu : Beerse Flanders
Société : Johnson and Johnson

Scientific and Regulatory literature) to create new opportunities within Pharmaceutical & Material Sciences...quality assurance and regulatory to select,..

Postuler


Associate Director in Solid State Sciences & Characterization

Lieu : Beerse Flanders
Société : Johnson and Johnson

..quality assurance and regulatory to select,..In Belgium (Beerse) there is a vacancy for an Associate Director in Solid State Sciences & Characterization ...

Postuler


Associate Director in Solid State Sciences & Characterization

Lieu : Beerse Flanders
Société : Johnson and Johnson

Scientific and Regulatory literature) to create new opportunities within Pharmaceutical & Material Sciences...In Belgium (Beerse) there is a vacancy for an Associate Director in Solid State Sciences & Characterization ...

Postuler


Associate Director in Solid State Sciences & Characterization

Lieu : Beerse Flanders
Société : Johnson and Johnson

In Belgium (Beerse) there is a vacancy for an Associate Director in Solid State Sciences & Characterization ...

Postuler


Associate Director/Director, Regulatory

Lieu : Ghent Flanders
Société : Argenx

This role serves as a close business partner and facilitator of regulatory activities and is expected to contribute to developing sound regulatory strategies globally...

Postuler | Plus d'offres Associate Director/Director, Regulatory
Plus d'offres - Ghent


Associate Director/Director, Regulatory

Lieu : Ghent Flanders
Société : Argenx

and distribution teams to ensure regulatory input is provided in a timely matter to support business decisionsServe as the conduit between strategy within the assigned project team and the broader global regulatory and development teamsDesired Skills and Experience:Minimum 10..

Postuler | Plus d'offres Associate Director/Director, Regulatory
Plus d'offres - Ghent


Associate Director/Director, Regulatory

Lieu : Ghent Flanders
Société : Argenx

and post-approval regulatory activities,..In close collaboration with other functions and the broader regulatory team,..

Postuler | Plus d'offres Associate Director/Director, Regulatory
Plus d'offres - Ghent


Associate Director/Director, Regulatory

Lieu : Ghent Flanders
Société : Argenx

and coordinate across disciplines to ensure timely filingsOversee regulatory affairs vendors involved in marketing authorization filings and help ensure high quality interactions with regulatorsWorking with the rest of the argenx regulatory team,..

Postuler | Plus d'offres Associate Director/Director, Regulatory
Plus d'offres - Ghent


Associate Director/Director, Regulatory

Lieu : Ghent Flanders
Société : Argenx

and other areas as requestedProvide regulatory leadership with post-approval activities including application maintenance activities such as drug registration and listing,..

Postuler | Plus d'offres Associate Director/Director, Regulatory
Plus d'offres - Ghent


Director of Regulatory Compliance - Enterprise Risk - Sector Focus Industries

Lieu : Machelen Flanders
Société : EY

Extensive knowledge and understanding of regulatory frameworks in multiple jurisdictions and industries...Strong business development acumen with a proven track record in developing business in the regulatory compliance space...

Postuler


Director of Regulatory Compliance - Enterprise Risk - Sector Focus Industries

Lieu : Machelen Flanders
Société : EY

drive and grow our corporate Regulatory Compliance service...this is the perfect opportunity for an individual with a strong background in Regulatory Compliance and a nose for business development to make a mark in a leading global professional services firm that is committed..

Postuler


Director of Regulatory Compliance - Enterprise Risk - Sector Focus Industries

Lieu : Machelen Flanders
Société : EY

..or regulatory body...drive and grow our corporate Regulatory Compliance service...we do not discriminate on the basis of race,..

Postuler


Director of Regulatory Compliance - Enterprise Risk - Sector Focus Industries

Lieu : Machelen Flanders
Société : EY

Your Key Responsibilities Lead the Regulatory Compliance team and develop strategic plans to drive business growth within EY Consulting / Enterprise Risk...

Postuler


Director of Regulatory Compliance - Enterprise Risk - Sector Focus Industries

Lieu : Machelen Flanders
Société : EY

Extensive knowledge and understanding of regulatory frameworks in multiple jurisdictions and industries...EY is seeking an experienced Director of Regulatory Compliance to join our Consulting Enterprise Risk division...

Postuler


Director of Regulatory Compliance - Enterprise Risk - Sector Focus Industries

Lieu : Machelen Flanders
Société : EY

Extensive knowledge and understanding of regulatory frameworks in multiple jurisdictions and industries...or regulatory body...

Postuler


Director of Regulatory Compliance - Enterprise Risk - Sector Focus Industries

Lieu : Machelen Flanders
Société : EY

EY is seeking an experienced Director of Regulatory Compliance to join our Consulting Enterprise Risk division...

Postuler


Director of Regulatory Compliance - Enterprise Risk - Sector Focus Industries

Lieu : Machelen Flanders
Société : EY

this is the perfect opportunity for an individual with a strong background in Regulatory Compliance and a nose for business development to make a mark in a leading global professional services firm that is committed to building a better working world...

Postuler


Associate Director, Clinical Trial Lead (m/f/d)

Lieu : Overijse Flanders
Société : Merck KGaA, Darmstadt, Germany

typically Ph III and registrational/pivotal studies in mixed sourcing models...Demonstrates skills in successfully leading large-sized global project teams in a matrix organization and directs,..

Postuler


Associate Director, Clinical Trial Lead (m/f/d)

Lieu : Overijse Flanders
Société : Merck KGaA, Darmstadt, Germany

aligns clinical trial team with organizational goals and objectives of the Clinical Operations Team and/or Global Program Team.Filters,..

Postuler


Associate Director, Clinical Trial Lead (m/f/d)

Lieu : Overijse Flanders
Société : Merck KGaA, Darmstadt, Germany

local regulatory guidance including ICH-GCP;..able to predict the result of action in advance and evaluate options to achieve goals. Who you areAt least 10-12 years in clinical research in a CRO or Pharmaceutical/Biotechnology Industry environment with at least 7 years of in-depth ..

Postuler


Associate Director, Clinical Trial Lead (m/f/d)

Lieu : Overijse Flanders
Société : Merck KGaA, Darmstadt, Germany

..local regulatory guidance including ICH-GCP;..able to predict the result of action in advance and evaluate options to achieve goals. Who you areAt least 10-12 years in clinical research in a CRO or Pharmaceutical/Biotechnology Industry environment with at least 7 years of in-dept..

Postuler


Associate Director, Clinical Trial Lead (m/f/d)

Lieu : Overijse Flanders
Société : Merck KGaA, Darmstadt, Germany

local regulatory guidance including ICH-GCP;..Requires expert knowledge and experience in own discipline and beyond which may also require good market and competitor knowledge.Strong leadership competencies and influencing skills.Proven team dynamic knowledge and skills and ability ..

Postuler


Associate Director, Clinical Trial Lead (m/f/d)

Lieu : Overijse Flanders
Société : Merck KGaA, Darmstadt, Germany

..local regulatory guidance including ICH-GCP;..Demonstrates skills in successfully leading large-sized global project teams in a matrix organization and directs,..

Postuler


Associate Director, Clinical Trial Lead (m/f/d)

Lieu : Overijse Flanders
Société : Merck KGaA, Darmstadt, Germany

MS,..PMP) desirable.Proven experience in all aspects of clinical study planning and startup (including budget and resource planning) and in executing the complete range of clinical study activities,..

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