39 offres d'emploi Associate Director, Clinical Trial Lead (m f d) - be |
|
Site source : Talent BE
Lieu : Overijse Flanders
Société : Merck KGaA, Darmstadt, Germany
Détail de l'offre : 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,..
Postuler |
Site source : Talent BE
Lieu : Overijse Flanders
Société : Merck KGaA, Darmstadt, Germany
Détail de l'offre : nonclinical & pharmaceutical development,..audit & inspection leadership- interviewee & responses.Contribute to non-study -related initiatives in addition to study assignments...
Postuler |
Site source : Talent BE
Lieu : Overijse Flanders
Société : Merck KGaA, Darmstadt, Germany
Détail de l'offre : timelines and quality standards agreed upon by Governance Committees.As a core member of the Clinical Operations Team and leader of the Clinical Trial Team,..
Postuler |
Site source : Talent BE
Lieu : Overijse Flanders
Société : Merck KGaA, Darmstadt, Germany
Détail de l'offre : aligns clinical trial team with organizational goals and objectives of the Clinical Operations Team and/or Global Program Team.Filters,..
Postuler |
Site source : Talent BE
Lieu : Overijse Flanders
Société : Merck KGaA, Darmstadt, Germany
Détail de l'offre : Demonstrates skills in successfully leading large-sized global project teams in a matrix organization and directs,..
Postuler |
Site source : Talent BE
Lieu : Overijse Flanders
Société : Merck KGaA, Darmstadt, Germany
Détail de l'offre : 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 knowledge and experience in clinical
Postuler |
Site source : Talent BE
Lieu : Overijse Flanders
Société : Merck KGaA, Darmstadt, Germany
Détail de l'offre : Demonstrates skills in successfully leading large-sized global project teams in a matrix organization and directs,..
Postuler |
Site source : Talent BE
Lieu : Overijse Flanders
Société : Merck KGaA, Darmstadt, Germany
Détail de l'offre : including some knowledge of interfaces and interdependencies of clinical development with other functions (e.g.,..
Postuler |
|
Site source : Talent BE
Lieu : Overijse Flanders
Société : Merck KGaA, Darmstadt, Germany
Détail de l'offre : 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 knowledge and experience in clinical
Postuler |
Site source : Talent BE
Lieu :
Société : Genmab
Détail de l'offre : Prior experience working in Medidata Rave in the core configuration environment or system implementation is preferred. SAS programming experience or experience programming custom functions is advantageous.Responsibilities:Lead and participate in the development and maintenance o..
Postuler |
Site source : Talent BE
Lieu :
Société : Genmab
Détail de l'offre : Prior experience working in Medidata Rave in the core configuration environment or system implementation is preferred. SAS programming experience or experience programming custom functions is advantageous.Responsibilities:Lead and participate in the development and maintenance o..
Postuler |
Site source : Talent BE
Lieu :
Société : Genmab
Détail de l'offre : manage and govern clinical data standards;..and clinical data standards development and maintenance.Experience in pharmaceutical industry CDASH/SDTM data standards management and implementation required.Demonstrated experience in all phases of drug development and clinical..
Postuler |
Site source : Talent BE
Lieu :
Société : Genmab
Détail de l'offre : maintenance and adherence to Genmab’s clinical data standards including eCRFs,..global librarian) and has a track record in applying own knowledge to significantly improve efficiencies.Ability to work in a fast-paced environment and be influential in reaching prompt decisions to s..
Postuler |
Site source : Talent BE
Lieu :
Société : Genmab
Détail de l'offre : maintenance and adherence to Genmab’s clinical data standards including eCRFs,..Prior experience working in Medidata Rave in the core configuration environment or system implementation is preferred. SAS programming experience or experience programming custom functions is advan..
Postuler |
Site source : Talent BE
Lieu : Beerse Flanders
Société : Johnson and Johnson
Détail de l'offre : and CROs * Develops credible relationships with senior leaders,..and leading clinical data discussions * Mentorship of less experienced team members and may have direct reporting/people management accountability Principal Relationships Con..
Postuler | Plus d'offres Director, Clinical Project Scientist
Plus d'offres - Beerse |
Site source : Talent BE
Lieu : Beerse Flanders
Société : Johnson and Johnson
Détail de l'offre : • Members of the Clinical and Cross Functional Trial teams • Members of Oncology TA • Cross Functional Senior Management Contacts outside the Company:..
Postuler | Plus d'offres Director, Clinical Project Scientist
Plus d'offres - Beerse |
Site source : Talent BE
Lieu : Beerse Flanders
Société : Johnson and Johnson
Détail de l'offre : analysis * Reviews and maintains protocol specifications in alignment with standard operating procedures * Guides and mentors less experienced team members in adherence to clinical research guidelines and safety procedures * Maintains expertise on cl..
Postuler | Plus d'offres Director, Clinical Project Scientist
Plus d'offres - Beerse |
Site source : Talent BE
Lieu : Brussels Brussels
Société : Proclinical
Détail de l'offre : they're seeking several Clinical Operations Program Directors to strengthen our clients Global Clinical Trial Operations team...
Postuler |
Site source : Talent BE
Lieu : Brussels Brussels
Société : Proclinical
Détail de l'offre : they're seeking several Clinical Operations Program Directors to strengthen our clients Global Clinical Trial Operations team...
Postuler |
Site source : Talent BE
Lieu : Brussels Brussels
Société : Proclinical
Détail de l'offre : - Rare diseases experience would be a plus.About Proclinical:..This role is crucial in driving the execution of the clinical program in collaboration with the Clinical Development department.Key Responsibilities:..
Postuler |
Site source : Talent BE
Lieu : Brussels Brussels
Société : Proclinical
Détail de l'offre : - Lead the Clinical Development meetings,..Project Manager and other Clinical Development representatives...
Postuler |
Site source : Talent BE
Lieu :
Société : Astellas Pharma Inc.
Détail de l'offre : Strong clinical study management skills (including project and financial management) with good knowledge of global drug development,..
Postuler | Plus d'offres Associate Director, Study Management |
Site source : Talent BE
Lieu :
Société : Astellas Pharma Inc.
Détail de l'offre : product lifecycle management and clinical study design...About this role:As the Associate Director Study Management,..
Postuler | Plus d'offres Associate Director, Study Management |
Site source : Talent BE
Lieu :
Société : Astellas Pharma Inc.
Détail de l'offre : study sites and vendors for assigned clinical studies...About this role:As the Associate Director Study Management,..
Postuler | Plus d'offres Associate Director, Study Management |
Site source : Talent BE
Lieu :
Société : Astellas Pharma Inc.
Détail de l'offre : Direct key initiatives and studies to support Clinical Operations including budgeting and planning,..About this role:As the Associate Director Study Management,..
Postuler | Plus d'offres Associate Director, Study Management |
|
