416 offres d'emploi Regulatory Affairs Expert - |
|
Lieu : Machelen Flanders
Société : Johnson and Johnson
§ You have minimum 5 years of relevant experience in regulatory legal work in the life sciences industry,..minimum of 7 years of post-qualification legal experience of which at least 5 years also in regulatory legal matters in the pharmaceutical / medical devices / life scie..
Postuler |
Lieu : Machelen Flanders
Société : Johnson and Johnson
• Experience with regulatory legal support of medical devices is considered an asset...• You have experience with regulatory legal support of innovative medicines.Experience with advanced therapy medicinal products is considered an asset...
Postuler |
Lieu : Machelen Flanders
Société : Johnson and Johnson
..• You have experience with regulatory legal support of innovative medicines...working closely together with various functional groups on regulatory legal matters across the region,..
Postuler |
Lieu : Machelen Flanders
Société : Johnson and Johnson
Governmental Affairs & Policy,..The Johnson & Johnson EMEA Law Department is recruiting a Senior Legal Counsel to provide regulatory legal support to its healthcare businesses.The position will be based preferably in Belgium (Diegem or Beerse);..
Postuler |
Lieu : Machelen Flanders
Société : Johnson and Johnson
Through our expertise in Innovative Medicine and MedTech,..minimum of 7 years of post-qualification legal experience of which at least 5 years also in regulatory legal matters in the pharmaceutical / medical devices / life sciences sector...
Postuler |
Lieu : Machelen Flanders
Société : Johnson and Johnson
The Johnson & Johnson EMEA Law Department is recruiting a Senior Legal Counsel to provide regulatory legal support to its healthcare businesses.The position will be based preferably in Belgium (Diegem or Beerse);..
Postuler |
Lieu : Machelen Flanders
Société : Johnson and Johnson
Medical Affairs,..§ You have minimum 5 years of relevant experience in regulatory legal work in the life sciences industry,..
Postuler |
Lieu : Machelen Flanders
Société : Johnson and Johnson
minimum of 7 years of post-qualification legal experience of which at least 5 years also in regulatory legal matters in the pharmaceutical / medical devices / life sciences sector.Excellent written / spoken English...
Postuler |
|
Lieu : Brussels Brussels
Société : Lime
identifying and advising on pertinent issuesPreferred Qualifications 5+ years experience in government affairs,..
Postuler | Plus d'offres Public Affairs Senior Manager
Plus d'offres - Brussels |
Lieu : Brussels Brussels
Société : Lime
and community groups to align Lime's social mission with existing local initiatives.Track and advise on important changes in regulatory or legislative matters affecting your market.About you:A public affairs expert with political acumen and a strong understanding of po..
Postuler | Plus d'offres Public Affairs Senior Manager
Plus d'offres - Brussels |
Lieu : Brussels Brussels
Société : Lime
You will contribute to drive our policy and public affairs work in Benelux in a dynamic and diverse team...and community groups to align Lime's social mission with existing local initiatives.Track and advise on important changes in regulatory or legislative matters affecting ..
Postuler | Plus d'offres Public Affairs Senior Manager
Plus d'offres - Brussels |
Lieu :
Société : Chronos Consulting
country) conform to Good Clinical Practice regulations and standardsEnsure adherence to protocols and compliance with regulatory (FDA/ICH/ISO/GCP) guidelines as well as SOP proceduresIdentify clinical training needs and develop training materials for in-house and clinical site use..
Postuler |
Lieu :
Société : Chronos Consulting
country) conform to Good Clinical Practice regulations and standardsEnsure adherence to protocols and compliance with regulatory (FDA/ICH/ISO/GCP) guidelines as well as SOP proceduresIdentify clinical training needs and develop training materials for in-house and clinical site use..
Postuler |
Lieu :
Société : Chronos Consulting
Biopharmaceutical experience would provide a strong advantage3) Additional 4+ years direct experience in clinical trial management4) Solid track record in successfully executing Phase I – III clinical trials5) Demonstrated expert knowledge and comprehensive understanding of applic..
Postuler |
Lieu : Brussels Brussels
Société : Dentons Global Advisors
we help clients engage with governments and regulatory bodies,..with a minimum of 3 days per week in the office) Responsibilities Research and analysis on a range of policy topics Organising and participating in meetings and events Supporting in the delivery of public affairs..
Postuler |
Lieu : Brussels Brussels
Société : Dentons Global Advisors
we help clients engage with governments and regulatory bodies,..economics…) Previous internship or experience in the EU institutions or in public affairs Knowledge of the EU institutions and of EU decision-making Enthusiasm for EU policy-making and a willingness to learn Un..
Postuler |
Lieu :
Société : Chronos Consulting
country) conform to Good Clinical Practice regulations and standardsEnsure adherence to protocols and compliance with regulatory (FDA/ICH/ISO/GCP) guidelines as well as SOP proceduresIdentify clinical training needs and develop training materials for in-house and clinical site use..
Postuler |
Lieu :
Société : Chronos Consulting
They are looking for a Clinical Affairs Program Manager Europe...country) conform to Good Clinical Practice regulations and standardsEnsure adherence to protocols and compliance with regulatory (FDA/ICH/ISO/GCP) guidelines as well as SOP proceduresIdentify clinical training n..
Postuler |
Lieu :
Société : Chronos Consulting
country) conform to Good Clinical Practice regulations and standardsEnsure adherence to protocols and compliance with regulatory (FDA/ICH/ISO/GCP) guidelines as well as SOP proceduresIdentify clinical training needs and develop training materials for in-house and clinical site use..
Postuler |
Lieu :
Société : Chronos Consulting
country) conform to Good Clinical Practice regulations and standardsEnsure adherence to protocols and compliance with regulatory (FDA/ICH/ISO/GCP) guidelines as well as SOP proceduresIdentify clinical training needs and develop training materials for in-house and clinical site use..
Postuler |
Lieu :
Société : Chronos Consulting
take corrective actions where necessary to address issuesDevelops budget for all clinical projects and adhere to company financial goalsEnsure clinical results are interpreted and documented clearly and concisely for regulatory submissions and publicationsDevelop,..
Postuler |
Lieu :
Société : BeiGene
and field resources for external use by Global Medical Affairs.Liaise with Global Publication Planning Leads and monitor the medical literature and conference abstracts for new reports in the therapeutic area for inclusion in Medical Affairs resourcesIncorporate insights into..
Postuler |
Lieu :
Société : BeiGene
in collaboration with clinical subject matter experts and MRC members and administratorsContribute to annual training planning cycles and support the development of global training projects and initiativesAdhere to BeiGene SOPs,..
Postuler |
Lieu :
Société : BeiGene
..and stakeholder expertise to identify,..and update materials appropriatelyCollaborate with Global Medical Affairs stakeholders to ensure global resources meet regional needs and develop local or country-specific resources as needed Ensure that key data statements and conclu..
Postuler |
Lieu : Brussels Brussels
Société : Dentons Global Advisors
we help clients engage with governments and regulatory bodies,.. Network to deepen professional expertise and knowledge...
Postuler |
|
