13 job matcher din søgning
Novo Nordisk A/S, Bagsværd
Are you interested in clinical trials, operational project management and pharmacovigilance? Do you want to cooperate with stakeholders across the organisation?
As an Event Adjudication Adviser, you will be a driving factor between Safety Operations, Data Management, Global Development and external service providers Clinical research organisations (CROs) dealing with event adjudication in selected clinical development projects. You will make the first assessment of the events and ensure that all documentation is made timely available for the final event adjudication.
Indrykket 23. maj
We are looking for a colleague with passion for quality assurance to join the GLP QA team within QA & Knowledge Management as a QA Scientist.
As a QA Scientist, you will be expected to:
- Audit study plan, study data and study reports from our analytical laboratories or from contract research organisations.
- Lead audits of contract research organisations often placed in Europe or US.
- Be a QA contact person for a specific analytical laboratory.
We offer a challenging position in a dynamic department with dedicated colleagues.
Indrykket 18. maj
Maersk Line, Copenhagen
Are you an engineer comfortable working with a wide range of data technologies and platforms? Do you understand the day-to-day obstacles to effective data science and software development work? This is an opportunity to join Maersk's Digital organisation as our Data Engineering Lead and drive digital transformation at a globally respected, industry leading brand.
Your responsibilities will be to:
- Lead and coach a team of talented data engineers tasked with leveraging a scalable, performant data engineering ecosystem for internal and external app development.
- Craft a meaningful vision for the team and ensure achievement of immediate term goals through teamwork and high standards
- Represent the Data Engineering group to various stakeholders with myriad data and analytics needs
Indrykket 17. maj
We are looking for a Quality Manager (QM) to contribute to sponsor oversight of Lundbeck’s interventional clinical studies (phase II and onwards). The Quality Oversight Team contributes to ensure high quality of Lundbeck’s clinical studies and to ensure oversight with respect to compliance with ICH-GCP guidelines, regulatory requirements, corporate SOPs, the study protocols and other study specific procedures – both by remote quality oversight as well as by conducting Sponsor Visits to investigational sites participating in the Lundbeck clinical studies.
You will also be involved in following up on audit CAPAs as well as collaborate with the CAPA team anchor ensuring efficient handling and communication of CAPAs. You will work in close collaboration with the other QMs as well as International Study Managers (ISM), Clinical Quality Assurance (CQA) and CROs.
Indrykket 11. maj
LEO Pharma, Ballerup
LEO Pharma relies on a number of global Contract Research Organisations (CROs) and Contract Manufacturing Organisations (CMOs) to execute our clinical trials with quality compliance within agreed timelines. Would you like to play a key role in supporting our growing portfolio within the clinical outsourcing area? We are looking for a new colleague in Clinical Vendor Management.
You will manage all aspects of collaborations with our external partners; from assessing the need to outsource an activity, scouting for the optimal vendors – ensuring a match to LEO’s requirements, to contractual negotiation, performance monitoring and follow-up. You will collaborate and liaise closely with various internal stakeholders such as Clinical Project Managers, Clinical Operational Leads, R&D Quality, Global Procurement, R&D Legal, etc.
Indrykket 8. maj
Symphogen A/S, Ballerup
The position as Lead Clinical Research Associate (Lead CRA) offers a unique possibility to take part in the clinical development of Symphogen's antibody products.
As Lead CRA, you will work in close collaboration with the Clinical Trial Manager (CTM) and the Clinical Trial Team in supervising, monitoring, and supporting the administration and pro-gress of clinical trials.
- A challenging and versatile job in an innovative, flexible, focused and committed biotech environment
- Competitive salary based on qualifications
Indrykket 5. maj
I am looking for a Manager that can help my client, a world leading company within there field, start a department for production of material for clinical
NonStop Recruitment, København, Denmark
Jobsincopenhagen, 25. maj
Klinisk AfprøvningsTeam (KAT) ved Hæmatologisk Klinik opnormeres og har en 32-37 timers stilling (efter aftale) ledig pr. 1....
Region Hovedstaden, Region Hovedstaden
Region Hovedstaden, 23. maj
Vi søger en læge med interesse for endokrinologi og kardiologi til et projekt, der skal undersøge betydningen af glukose, frie fede syrer,...
Region Hovedstaden, Region Hovedstaden
Region Hovedstaden, 18. maj
Join an international sponsor company to work mainly on Oncology studies. Exciting fully home based option for an experienced CRA located within Greater
i-Pharm Consulting, Copenhagen
Jobsincopenhagen, 18. maj
Den Kliniske Forsknings Enhed i Hæmatologisk Afdeling søger en projektsygeplejerske til at varetage opgaver i forbindelse med...
Region Hovedstaden, Herlev
Region Hovedstaden, 17. maj
Radek Weichert at Skills Alliance is recruiting for a ( Senior ) Clinical Research Associate to join a Medium size global CRO in Denmark. It is a friendly
Jobsincopenhagen, 12. maj
Nomeco HealthCare Logistics er lægemiddelindustriens nationale og internationale outsourcing-partner inden for sundhedslogistik.
Nomeco A/S, København
StepStone, 8. maj