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As a senior global regulatory lead, you will be responsible for our gene therapy project's regulatory activities and strategies focused on treating severe cancer diseases...
To excel in the role of our new Director - Global Launch Lead, your primary responsibility will be overseeing the launch of one of our products. This entails leading a...
The Senior Clinical Trial Manager (CTM) serves as the clinical functional lead, accountable for the clinical monitoring/site management delivery of assigned tasks and project(s) as...
Be key account manager for CMOs for labeling and packaging activities of final drug product, transfer to and storage at drug depot, as well as for distribution logistics from drug...
Provide internal and external medical support for the Oncology portfolio by being an expert on products, patient treatment trends and scientific activities within the disease area,...
As our new Director, Global PV Operations you will become responsible for PV Operations activities and provide strategic and operational PV/quality/safety support for Ascendis...
Responsibilities include the implementation of outcomes research strategies, health economics research planning, and process improvements to ensure patient access to Daiichi...
You will ensure seamless management of clinical projects; You will be responsible for the planning and executing of clinical trials in phases 1-4 within all of Ferring’s...
You will contribute to clinical study reports, data analysis review, publications, and study strategic development; You will lead the trial team with representation from relevant...
As a Regulatory Affairs Manager you will be responsible and accountable for all local operational aspects of regulatory submissions providing planning and technical support for...
Oversees development and implementation of worldwide regulatory strategies for projects and issues affecting new product or new indication development; Leads interactions and...
Are you ready to play a role in public health protection and contribute to the quality of medicines worldwide? Do you think you have the right mix of scientific, relationship...
Act as a specialist in the area of oncology. Represent Regulatory Affairs internally working on a collaborative basis both within Europe and globally as a member of a...
You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics...
The main purpose of this position is establishing and maintaining a domestic Pharmacovigilance (PV) unit, being responsible for carrying out all PV activities as described in...
he Senior Manager of R&D Quality will proactively promote compliance to Good Clinical Practice (GCP) regulations by providing Clinical and Research Development teams compliance...
The Clinical Trial Supply Manager (CTSM) represents product supply in the Clinical Study Teams and drives the development and execution of effective product supply strategies in...
The Sr. Manager Medical Affairs Oncology Medical Spain & Portugal is responsible for supporting the development and execution of the national medical strategy and programs that...
The Associate Medical Director Clinical Science Haemophilia is responsible for Sobi’s clinical development activities for one or more product(s)/indication(s) in the therapeutic...
Providing Clinical Devices Quality input to cross functional teams dealing with complex and important projects and issues. Providing mentoring and guidance to other members of the...
Responsible for execution for medicinal products supervised designing CMC strategies and providing guidance to ensure regulatory compliance in time and quality; Set up, review and...
Performing Data Management of Clinical Safety & Pharmacovigilance (CSPV) information of ICSR from clinical trials and marketed products. Ensure regional ICSR team compliance with...
As our new Associate Director RA Device, you will be driving the regulatory strategy for device constituent parts of combination products and use your device regulatory experience...
Collaborate with and provide global support for all R&D sites as part of a newly formed global CMC management organisation on small-molecule API development projects from...
Support the Medical Leadership in implementing medical strategy applicable to assigned therapeutic area; Develop and deliver an annual medical clinical plan in line with the...