This job at Stryker is not available
We're sorry, the job you are looking for at Stryker on EuroPharmaJobs has expired.
Click here to see more jobs at Stryker.
We still have many live jobs. Click below for similar jobs in:
or go to our job search page.
Similar jobs selected for you
-
Top Job
Independently develop and implement regulatory submission strategies for assigned complex programs and/or portfolio of products; Represent the Regulatory Affairs function in...
Posted 7 days ago -
Top Job
This person will actively participate in/lead a broad range of medical affairs activities, including preparation of support to investigator initiated research (IIR) programs,...
Posted 13 days ago -
Top Job
This position is responsible for providing leadership and establishing strategy and implementing clinical drug efforts for Incyte's oncology products (Phase I though Phase III)....
Posted 27 days ago -
Top Job
Provide scientific and technical leadership within the cluster of countries for our COVID 19 vaccine and future vaccination programs; Develop and foster relationships with external...
Posted 35 days ago -
You will typically lead multiple components of clinical trial programs in pediatric oncology clinical development. You may also act as the Physician Responsible on certain...
Posted 4 days ago -
The Country Trials Manager is responsible for study startup deliverables for assigned studies at a country level that are of moderate to high complexity, country level...
Posted 10 days ago -
Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and...
Posted 12 days ago -
Scientific Affairs Manager, GSA (Germany, Switzerland and Austria)
Rhythm PharmaceuticalsHome-based, GermanyBe a trusted scientific partner to key external experts by conducting timely, appropriate, and frequent scientific exchanges to enhance the understanding of the scientific and...
Posted 12 days ago -
The Director, Country Head, Quality Assurance is responsible to ensure that the organization and monitoring of the company's vaccine/pharmaceutical operations are conducted in...
Posted 17 days ago -
The PV Director shall be responsible for the establishment and maintenance of the company’s PV system and therefore shall have sufficient authority to influence the performance...
Posted 19 days ago -
Senior Manager Medical Affairs THV (Grants and Clinical Trial Programs)
Edwards LifesciencesMultiple Locations, Multiple CountriesThe "Senior Manager Medical Affairs THV" will manage a team with responsible for processes within Medical Affairs (e.g., grants, clinical trial process operations) and Evidence...
Posted 24 days ago -
You will be responsible for the set-up and progress of clinical studies within the Nordic and Baltic (NOBA) countries, ensuring compliance with Quality Documents and regulations in...
Posted 25 days ago -
You prepare and submit applications for new marketing authorisations/registrations and respond to questions in a timely and accurate manner; You compile and update dossiers for...
Posted 26 days ago -
You will be the primary contact to internal and external stakeholders on behalf of Teva Global Regulatory Affairs EU for assigned responsibilities. You will be responsible for...
Posted 26 days ago -
Ensure that strategic aims of the Company are met within Mid Europe cluster and in Scandinavia/Nordics by providing high quality medical and scientific input and by active...
Posted 28 days ago -
Proactively managing CMC aspects of one or more development programs including overseeing preparation and submission of global CMC submissions, including clinical trial...
Posted 31 days ago -
The Medical Science Manager will pre/launch novel therapies targeting genetic and immunological drivers of cancer. You will be part of a new medical team in EU, that strives to be...
Posted 32 days ago -
Provide effective operational and regulatory support for assigned regulatory submission and maintenance activities, including preparation and submission of regulatory dossiers,...
Posted 33 days ago -
Represent GRA as a core member of the cross functional project team and Global Brand team and provides overall regulatory input for the project(s) globally. Be the single point of...
Posted 34 days ago -
You prepare and submit applications for new marketing authorisations/registrations and respond to questions in a timely and accurate manner; You compile and update dossiers for...
Posted 38 days ago -
As Quality and Regulatory Manager your mission will be to lead and manage the implementation and maintenance of the CHC Affiliate Quality System (covering GxP and other regulated...
Posted 39 days ago -
Manage clinical project timelines, milestones, schedules and updates during all project stages; Report project status updates and progress for a designated region; participate in...
Posted 39 days ago -
As Head of Clinical Development, you will be accountable to lead the overall execution of clinical programs, provide leadership, project management and program oversight for the...
Posted 40 days ago -
Posted 3 days ago
-
Posted 3 days ago
-
Posted 3 days ago
-
Posted 5 days ago
-
Posted 5 days ago
-
Posted 5 days ago
-
Posted 6 days ago
-
Jazz PharmaceuticalsOxford, United KingdomPosted 6 days ago
-
Posted 7 days ago
-
Posted 7 days ago
-
TevaBasel, SwitzerlandPosted 7 days ago
-
Posted 7 days ago
-
Posted 10 days ago
-
Posted 10 days ago
-
Posted 12 days ago
-
Posted 17 days ago
-
Posted 19 days ago
-
Posted 24 days ago
-
Posted 24 days ago
-
Posted 27 days ago
-
Posted 28 days ago
-
Posted 31 days ago
-
Posted 31 days ago
-
Posted 32 days ago
-
Posted 32 days ago
-
Posted 33 days ago
-
AlconMultiple Locations, Europe, Multiple CountriesPosted 33 days ago
-
Posted 33 days ago
-
AlconMultiple Locations, Europe, Multiple CountriesPosted 33 days ago
-
Posted 35 days ago
-
Posted 38 days ago
-
Posted 38 days ago
-
Posted 38 days ago
-
Posted 39 days ago
-
Posted 41 days ago
-
Posted 41 days ago
-
Posted 42 days ago
