Risultati della ricerca: 191 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
...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
...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
Novartis Pharma AG
Basilea BS
24 giorni fa
...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
...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
...Experience with with clinical trial CMC and R&D accruals/prepaids (CRO fees investigator fees lab fees and other vendor costs) a... ...404 General Accounting compliance including:
Internal control documentation (maintenance of narratives control matrices/flowcharts)
When...
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 managing the medical relationship with Sponsors;...
Consigliato
Tempo pieno
Lavoro a turni
Novartis AG
Basilea BS
un mese fa
...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
...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
...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
...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...
Consigliato
...corresponding procedures.
Maintain cleanliness of the workplace.
Document all executed activities in a GMP compliant manner, both in electronic systems (SAPs) and on paper-based documentation.
Report any quality events or deviations to the Manager or deputy....
Consigliato
...and yearly financial statements following IFRS and OR standards (including the year-end statutory report in French)
Entering cash documents from plants in French-speaking Switzerland and reconciling bank accounts
Preparing VAT and withholding tax statements Regularly...
Consigliato
...corrective and preventive actions in consultation with QA
- Provide expert support to monitor, update, and adapt the GMP-relevant document landscape within pCMC
- Participating in the preparation and coordination of internal and health authority audits, as well as...
Consigliato
Paga oraria
...content, and potential genotoxic impurity determinations.
Documentation: Write up analytical methods for implementation and... ...guidelines.
Data Interpretation: Interpret and document analytical data from various stages including method development...
Apprendistato
...international study commissions/competitions or in the concept or implementation phase.
We look forward to receiving your application documents in digital form (PDF, no links to websites, only 1 attachment max. 10 MB file size) at ****@*****.***
If you have any...
Tempo pieno
...in Switzerland
Travel: no
Tasks and Responsibilities
Create and maintain command line and web/rest applications (design, document, develop, test and deploy)
Create scripts, customizations, templates to ensure speed of delivery
AWS Serverless Architecture...
Home office
Remote job
Lavoro urgente
Lavoro a turni
...trainings on new systems
Review and update SOPs, supporting documents, and procedures with the help of subject matter experts... ...local and global working and compliance processes and associated documentation
Requirements
Bachelor's degree or higher in chemistry...
Remote job
...Address business intelligence tickets and issues in a timely fashion
Manage user access and change management
Maintain documentations for all business intelligence processes
Profile:
~ University degree in IT Engineering /Computer Sciences or similar education...
