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LEO Pharma, Ballerup
Your overall focus is to secure a smoothly running operation within clinical trials and to support LEO Pharma’s 2025 strategy in which digitalisation plays an important part. You play a pivotal role in the daily system operation, and you are the indispensable link between IT and the business, identifying and translating business needs into specific system change requests, which you also ensure implementation of. Your primary tasks include – but are not limited
- Identifying and translating business needs into system changes and implement the changes
- Initiating and driving initiatives to monitor and improve data quality
- Coordinating data transfers across systems and maintain relevant system SOPs
Novo Nordisk A/S, Søborg
Being part of Novo Nordisk Research & Development means working at one of the world’s largest and most successful biopharmaceutical companies. This is the chance for a talented person with an interest in process optimisation and Standard Operating Procedure (SOP) development to join Global Clinical Compliance as our new Senior GCP Advisor.
Together with 8 colleagues, you will be responsible for ensuring that Novo Nordisk maintains one global clinical quality management system in compliance with GCP and other relevant external and internal requirements. You will be working in a dynamic department where flexibility on tasks is required. You will be GCP expert on the clinical SOPs in the SOP update process, provide GCP support to stakeholders and participate in cross-departmental working groups.
Ferring Pharmaceuticals A/S, Copenhagen
Driven by research and a passion for science Ferring Pharmaceuticals is a biopharmaceutical company dedicated to the development of innovative treatments that make a real difference in people’s lives all over the world.
Would you like to join us in a challenging position as QA Auditor with focus on GLP?
You will become a member of a highly motivated and dedicated team of auditors and compliance QA colleagues and your essential tasks will be to:
- Plan, conduct and report audits within GLP, covering study based audits and facility audits at Copenhagen site and sponsor audits at partners
- Report audit findings, trends and critical situations to Senior Management
- Interact with the Non-clinical R&D and compliance functions as part of follow up on audit observations and potential trends
Sanos Clinic A/S, Herlev
Sanos Clinic A/S is a newly established, dedicated clinical research clinic. In Sanos, we strive to deliver high quality clinical data in an innovative scientific environment, and to bring new medical treatments to the patients in need.
As a result of our growth, we are now looking for a physician qualified in Denmark to be a part of our team.
Your job as Clinical Research Physician is highly varied and will amongst other responsibilities include the following:
- oversee and be responsible for the conduct of clinical research that conforms with standards for Good Clinical Practice
- recruit and screen patients for clinical trials
- daily patient consultation
- contributing to trial protocol development and to feasibility assessments
Abbvie A/S, København
AbbVie A/S søger en engageret kollega til en 12-måneders ansættelse indenfor medicinsk afdeling. Du kan begå dig på både dansk og engelsk, forstår dig på processer, og elsker struktur. Du kommer til at være tovholder på mange forskellige kliniske kvalitetssikringsprojekter og studier på tværs af terapiområder, og vil ofte være AbbVie Danmarks kontaktperson til eksterne samarbejdspartnere. Du vil desuden komme til at arbejde tæt sammen med dine kolleger i Danmark, Europa og USA.
- Håndtere nationale postmarketing studier på tværs af terapiområder (f. eks. investigator-initierede studier, safamarbejdsstudier, register- og databaseprojekter og publikationer). Det kan inkludere site visits i forbindelse med opstart, opfølgning eller afslutning af studier, opfølgning på kontrakter, udbetalinger og andre milestones
- Assistere medicinske projekter, fx uddannelsesaktiviteter og kvalitetssikringsprojekter
Clinical Trial Administrator
Zealand Pharma A/S, Glostrup
Zealand Pharma A/S is seeking an experienced Clinical Trial Administrator to the Clinical Operations department. The department is responsible for setting up, overseeing and directing clinical trials from early development phases to market approval, typically with the use of and collaboration with Clinical Research Organizations (CROs).
The department is part of Clinical Development and is composed of a dynamic team with enthusiastic and professional colleagues. We have an open and respectful working environment with great team spirit and high quality mind-set, encouraging knowledge sharing and development of people and processes.
Due to the increased number of new trials to be initiated, we are seeking a new experienced colleague to join our team.
LEO Pharma, Ballerup
Would you like to play a key role in the development of our growing portfolio together with a friendly, ambitious and professional team of Clinical Trial Supply Professionals?
As a Clinical Trial Supply Professional you will join a very dedicated team, who is responsible for coordinating IMP outsourced related activities in connection with the conduct of Clinical Trials Phase I-IV. You will be working according to given company procedures and relevant GMP, GCP and regulatory requirements. You will also:
- Hold a strong understanding for IRT systems
- Provide input to the Clinical Trial Protocol
- Create SOPs and keep them updated
Klinisk Onkologi er et livskraftigt speciale i konstant udvikling.
Region Hovedstaden, København Ø
The University of Copenhagen announces a position as PostDoc at the Department of Nutrition, Exercise and Sports to commence as soon as...
Københavns Universitet, København Ø
Ved Rysensteen Gymnasium tilbydes 1 stilling som adjunkt/lektor fra 1. august 2018 inden for kemi og/eller fysik, gerne med...
Rysensteen Gymnasium, København V
Sektion for Klinisk og Forebyggende Ernæring ved Institut for Idræt og Ernæring på Københavns Universitet søger en diætist med...
Københavns Universitet, Frederiksberg C
Projektsygeplejerske til NSGO-CTU, Onkologisk Klinik, Rigshospitalet.
Region Hovedstaden, København Ø
Unilabs is seeking an experienced molecular biologist (Cand.
Unilabs A/S, København
Vi søger pr. 1. august 2018 , eller snarest muligt, en projektsygeplejerske, med en ugentlig arbejdstid på 37 timer.
Region Syddanmark, Odense C