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job description: responsible for ensuring Clinical trials are conducted in accordance with scientific, medical, and ethical principles, and within regulatory requirements/guidelines. responsible for Volunteer safety & accurate interpretation and .....
job description the main responsibility of the deployment manager is to coordinate and facilitate the delivery of produced Software developed within a program either to the Marketing department for general availability (ga) or to it Operations for .....
we are looking for highly motivated individual to help with support our Food Safety and quality organization. in this role you will be responsible for collecting and examining product in the Lab. technicians on staff will have a crucial role in .....
job description: the senior manager/Associate Director will be responsible for all Statistical activities of assigned Clinical projects, lead the Statistical team and act as point-of-contact on Statistical activities of Clinical .....
quality Coordinator (incoming material inspection) hours: 7:30 am - 4:00 pm; monday – friday (1st shift) new added details: - review, change and release inspection plans within the Laboratory information management module in SAP - build new .....
descriptionas an it recruiter you will have a passion for people combined with a strong Planning skill set and fast paced delivery. you will interact with everyone in the company and, as part of the Operations team, you will also work close to the .....
clariness is a fast-growing, international company with locations in germany, usa, serbia, and switzerland. we provide Clinical Trial acceleration services to the Pharmaceutical, biotechnical and Medical Device industry. we pioneer global patient .....
wer wir sind: seit über 10 jahren unterstützen wir pharma- und biotechunternehmen, CRO’s und medizingerätehersteller mit einer mission: medizinische innovationen schneller auf den markt bringen zu können. wir sind der Überzeugung, dass unser .....
aufgabengebiet klinische bewertungen nach meddev 2.7/1 und verordnung (eu) 2017/745 über medizinprodukte systematische literatursuche in einschlägigen datenbanken (embase, pubmed etc.) analyse wissenschaftlicher literatur auswertung klinischer .....