stillingsbetegnelse: Clinical Compliance Coordinator

jobbeskrivelse:
- Research & Development - Denmark - Søborg Being part of Novo Nordisk Research & Development means working at one of the world's largest and most successful biopharmaceutical companies. Our R&D organisation is vital to Novo Nordisk's continued growth and we always welcome talented people who would like to grow with us. If you are motivated by supporting the standardisation, optimisation and quality of the Novo Nordisk Clinical Trial Standard Operating Procedures (SOPs), you may be our new Clinical Compliance Coordinator in Global Clinical Compliance, Global Development. About the department Global Clinical Compliance is responsible for developing and maintaining the Clinical Trial Standard Operating Procedure (CT SOP) system, implementing external and internal regulation requirements, handling of nonconformities to CT SOPs. The department is divided into two teams. The open position is located in the GCC Process Support Team. Geographically the department is situated in Søborg. The job You will be responsible together with 14 colleagues 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 part of the team responsible for ensuring the administrative process for updating clinical trial Standard Operation Procedures (SOPs) in accordance with relevant schedules and requirements, and that the format of the documentation is in accordance with the required standards. You will participate in the planning and reporting of meetings for the group within Novo Nordisk responsible for maintaining Clinical Trial SOPs (The Clinical Trial SOP Council). Most of your responsibilities will be performed independently, but it is essential that you are an excellent team player who is able to help build a strong network with colleagues at headquarters and in affiliates. Qualifications You have a bachelor’s degree in business language (English) or equivalent or English as native language, and experience from a highly structured administrative position. You have experience within the clinical area in the pharmaceutical industry and SOP update coordination. You are an experienced user of MS Office and motivated to master new IT systems. The ideal candidate will have a strong quality mindset and a high degree of initiative and independence. You are well structured with an eye for detail without loosing the overview. To be successful in this job you need to be both service-minded, and a positive and creative team player. Contact For further information, please contact Malene Jagd Moe at +45 3079 3253. Deadline 22 November 2015.

Arbejdsgiver Navn: Novo Nordisk A/S

Arbejdsgiver telefonnummer: 44448888

Arbejdsgiver faxnummer: 44442314

Job kort beskrivelse: Journalistisk arbejde

land: Danmark

region: Hovedstaden

Kontrakt varighed: Fast

Kontrakttype: Fuldtid

krævede uddannelse: Ikke angivet

Kilde til jobtilbud: AMS, Offentlige arbejdsformidlinger, Danmark