Risultati della ricerca: 173 offerte di lavoro
...company F. Hoffmann La Roche based in Basel we are looking for a Documentations Specialist (m/f/d)
At Roche the Legal & Compliance team... ...repository GRACE/LCAR database and the physical archive in the document management.
Your main responsibilities will be:...
Consigliato
Tempo pieno
Remote job
...crucial role in reviewing and providing input on trial-related documents, contributing to the quality control of essential documents, and... ...in and contribute to trial team meetings.
Contribute to the CRO/Site selection process.
Perform accompanied visits, qualification...
Consigliato
Remote job
...responsible for driving the development of operational trial-related documents and procedures, as well as managing External Service Providers (... ...the deliverables towards the Contract Research Organization (CRO) and ESPs selected for the trial, to ensure compliance with...
Consigliato
...Manager is driving the development of the operational trial related documents and procedures, as well as setting-up the ESPs and supervising... ...the deliverables towards the Contract Research Organization (CRO) and ESPs selected for the trial, to ensure compliance with study...
Consigliato
Tempo pieno
Lavoro urgente
...coordinate the development and approval of study documents such as the protocol ICF studyspecific... ...oversight and the initial review of CRO and other thirdparty study vendor... ...satisfactory outcome.
Ensure that proper study documentation is maintained and archived in the...
Consigliato
Tempo pieno
...evaluate data provided by the CDMO
Review batch documentation assess deviations and contribute to batch release... ...project management and/or collaboration with CMO/CRO
~ Experience in establishing regulatory documents (Drug Product part of IMPD/INDs CTDs)
This interactive...
Consigliato
Tempo pieno
...reviewing relevant bioanalytical sections to regulatory and submission documents (e.g. IB, IND, CTD).
• Hire and lead a team of up to 40 (... ...and relevant (10+ years) GCP experience in a pharmaceutical, CRO or related industry.
• Demonstrated experience leading a regulated...
Consigliato
Tempo pieno
Temporaneo
Lavoro a turni
...Human, Proof of Concept, mechanistic and safety studies), and other documents such as investigators brochures.
• Responsible for clinical... ...leading early phase clinical trials; a senior role within a CRO responsible for managing the medical relationship with Sponsors;...
Consigliato
Tempo pieno
...Human, Proof of Concept, mechanistic and safety studies), and other documents such as investigators brochures.
• Responsible for clinical... ...leading early phase clinical trials; a senior role within a CRO responsible for leading the medical relationship with Sponsors;...
Consigliato
...activities for development projects performed at CRO/CMO site
selection and management of... ...ensure the availability of all required documentation
Write analytical overview reports and... ...of development sections of regulatory documents (e.g. CTD).
Support budgeting and...
Consigliato
Tempo pieno
...and suppliers
Supervising the deliverables towards the Contract Research Organization (CRO) and external providers
Leading the development of trial-related operational documents
Acting as the communication channel for the Clinical Research Associates (CRAs) to ensure...
Consigliato
...Experience designing and conducting early phase clinical trials including for inflammatory arthritis: either from pharma/biotech, a senior CRO role where you were responsible for the medical relationship and studies with Sponsors, or from a relevant academic medical center...
Consigliato
Tempo pieno
Lavoro post-doc
...apprenticeship as laboratory technician with at least 5 years of work experience, preferably in the area of DMPK in pharmaceutical industry or CRO/ESPs.
• Several years of working experience in animal experimentation is a must (e.g. valid accreditation with LTK1 course, FELASA...
Consigliato
Tempo pieno
Apprendistato
Orario flessibile
...and scientific knowledge and good practical knowledge of laboratory work
Expertise with software and computer tools, and good documentation practice
Benefits
~5 weeks vacation / 40h week
~ LinkedIn Learning with over 5000 trainings
~ Coverage of relevant...
Consigliato
Home office
...to the agile delivery of the implementation team
Design and implement application-level security configurations
Develop and document CIAM engineering patterns and guidelines.
Must haves:
Minimum of 7 years of experience working in IT and a minimum of 5 years...
Consigliato
In agosto
...parenteral manufacturing activities
Provide sound technical and quality assurance expertise for review and approval of quality related documents (e.g. SOPs, qualification, validation documents)
Requirements:
Degree in Engineering, Pharmacy, Biology,
Biochemistry,...
...Quality Operations Switzerland
Provide sound technical and quality assurance expertise for review and approval of quality related documents (e.g. SOPs, qualification, validation documents)
Partner with all stakeholders within the Clinical Supply Centre as well as with...
Temporaneo
Basilea BS
9 giorni fa
...Excellent communication skills in English and German
Are you interested? Do not hesitate and submit your complete application documents online today.
We also process applications by post, but will not return them for administrative reasons. We look forward to hearing...
Temporaneo
Lavoro urgente
Basilea BS
9 giorni fa
...Quality Operations Switzerland
• Provide sound technical and quality assurance expertise for review and approval of quality related documents (e.g. SOPs, qualification, validation documents)
• Partner with all stakeholders within the Clinical Supply Centre as well as...
Tempo pieno
Temporaneo
Home office
Basilea BS
9 giorni fa
...OverviewWe are looking to strengthen our young Qualification Management team with an affinity for technology, documents, an eye for detail and high quality standards. We operate in the pharmaceutical environment and are therefore required to comply with strict regulations...
