1163 offres d'emploi Associate Director Director, Regulatory - |
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Lieu : Société : Astellas Pharma Inc. ..Description Associate Director,..prepare and execute contingency plans for operational risk including patient recruitment,..
Postuler | Plus d'offres Associate Director, Study Management |
Lieu : Wavre Wallonia Société : 9627 Corixa Corporation nursing) and a master degree in Epidemiology with minimum of 2 years of advanced training or experience in infectious diseases and/or vaccine-related epidemiologyTwo or more years of experience leading pharmaco-epidemiologic research programs in a vaccine development environment.Preferred ..
Postuler | Plus d'offres Associate Director, Epidemiology (Vaccines) Plus d'offres - Wavre |
Lieu : Wavre Wallonia Société : 9627 Corixa Corporation including regulatory authorities,..marital status,..initiate and manage external collaborations globally.Basic Qualifications:A combination of academic training and practical experience in epidemiology is required...
Postuler | Plus d'offres Associate Director, Epidemiology (Vaccines) Plus d'offres - Wavre |
Lieu : Wavre Wallonia Société : 9627 Corixa Corporation ....including regulatory authorities,..development of policies/guidances related to epidemiology activities and also organizational work streamProvide support to Regional Epidemiologists as needed.Partner with external groups conducting epi and other community studies globally;..
Postuler | Plus d'offres Associate Director, Epidemiology (Vaccines) Plus d'offres - Wavre |
Lieu : Overijse Flanders Société : Merck KGaA, Darmstadt, Germany ..local regulatory guidance including ICH-GCP;..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,..
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Lieu : Overijse Flanders Société : Merck KGaA, Darmstadt, Germany local regulatory guidance including ICH-GCP;..typically Ph III and registrational/pivotal studies in mixed sourcing models...
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Lieu : Overijse Flanders Société : Merck KGaA, Darmstadt, Germany ..local regulatory guidance including ICH-GCP;..influences and motivates people;..regulatory,..Demonstrates skills in successfully leading large-sized global project teams in a matrix organization and directs,..
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Lieu : Overijse Flanders Société : Merck KGaA, Darmstadt, Germany 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 trial management..
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Lieu : Overijse Flanders Société : Merck KGaA, Darmstadt, Germany ..local regulatory guidance including ICH-GCP;..aligns clinical trial team with organizational goals and objectives of the Clinical Operations Team and/or Global Program Team.Filters,..
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Lieu : Overijse Flanders Société : Merck KGaA, Darmstadt, Germany local regulatory guidance including ICH-GCP;..from startup through final study report.Experience in multiple Therapeutic Areas (oncology and immunology preferred)Requires substantial to extensive professional experience in relevant disciplines and substantial project management expe..
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Lieu : Overijse Flanders Société : Merck KGaA, Darmstadt, Germany regulatory,..Leads the development of the clinical trial strategy while accountable for successful project execution and delivery of clinical operational plan within the budget,..
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Lieu : Overijse Flanders Société : Merck KGaA, Darmstadt, Germany ..local regulatory guidance including ICH-GCP;....MA,..risk,..Familiar with and considers overall business objectives and company strategy.Acts as a senior advisor and mentor within the team and beyond and serves as best practice resource within own discipline or as technical expert..
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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 abilit..
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Lieu : Ghent Flanders Société : Sanofi or gender identity.Watch our and check out our Diversity Equity and Inclusion actions at !#LI-EURAt Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values...
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Lieu : Ghent Flanders Société : Sanofi Discover .Better is out there...to optimize overall success and have a meaningful impact on patients’ lives.Main responsibilitiesLead a project/one or several indications of a project in clinical developmentWith minimal direction from senior statistical project leader or team leader,..
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Lieu : Ghent Flanders Société : Sanofi Statistical Project Leader (Associate Director),..sexual orientation,..regulatory authorities,..
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Lieu : Société : Genmab The Role & DepartmentThe Associate Director,..ensure alignment with regulatory requirements.Participate in relevant study and project team meetings as the Standards Technical SME and provide input for standards components,..
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Lieu : Société : Genmab ..and related regulatory requirementsKnowledge of SDTM best practices and tools (such metadata repository,..aligned with industry and regulatory best practices.Support filing and submission readiness activities;..
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Lieu : Société : Genmab ensure alignment with regulatory requirements.Participate in relevant study and project team meetings as the Standards Technical SME and provide input for standards components,..
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Lieu : Société : Genmab aligned with industry and regulatory best practices.Support filing and submission readiness activities;..and related regulatory requirementsKnowledge of SDTM best practices and tools (such metadata repository,..
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Lieu : Wavre Wallonia Société : 1849 GlaxoSmithKline Biologicals S.A. assay qualification reports and assay validation plans in agreement with quality by design principles and fulfill requirements from regulatory authorities...
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Lieu : Société : Genmab SOPs and regulatory requirements.Experience multi-tasking and project management experience a must.Requirements - what you must have:Bachelor's degree in science or related area 10+ years of significant Standards Experience and/or Clinical Data Management (CDM) experience in biotec..
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Lieu : Anderlecht Brussels Société : Coca-Cola Europacific Partners Monitor and assess vulnerabilities and associated risks and when needed develop and implement the remediation strategies for the entire CCEP and make sure they are in line with CCEP master plans and cost effective...
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Lieu : Heist-op-den-Berg Flanders Société : Organon including associated vaccination prerequisitesFlexible Work Arrangements:Shift:Valid Driving License:Hazardous Material(s):Number of Openings:..
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Lieu : Heist-op-den-Berg Flanders Société : Organon it is expected that you will visit the Oss site once every other week.ResponsibilitiesTakes a leading role in CMS projects executed independently or in close collaboration with fellow CMS team members and provides mentoring or coaching to the CMS team or internal customers throughout all p..
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