Suchergebnisse: 13 Stellenangebote
...functions, and ensure appropriate quality control of deliverables
• Supervise the deliverables towards the Contract Research Organization (CRO) and ESPs selected for the trial, to ensure compliance with study protocol and in accordance with scope of work; identify areas of...
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Vollzeit
Soforteinstellung
...collection and quality control of essential documents.
Participate in and contribute to trial team meetings.
Contribute to the CRO/Site selection process.
Perform accompanied visits, qualification visits, and initiation visits for assigned studies.
Conduct routine...
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Remote job
...on site is around 40-50%.
RESPONSIBILITIES AND TASKS
Review and provide input on requested trial-related documents and on any CRO prepared documents, e.g., protocol and protocol amendment, Informed Consent Form, Delegation of Authority, Case Report Forms Study-Specific...
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Freelance
Soforteinstellung
Remote job
...support for Organisation Clinical Trials:
- To represent CQA for organisations Clinical Trials
- To work closely with organisation, CRO Clinical Trial Teams during the preparation, execution, and closure of Organisation clinical trials
- To develop own area of...
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...biological compounds and biological drug product processes preferred.
~ Experience in project management and/or collaboration with CMO/CRO
~ Experience in establishing regulatory documents (Drug Product part of IMPD/INDs CTDs)
This interactive position requires...
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Vollzeit
...which requires a solid understanding of cutoffs and accruals.
Experience with with clinical trial CMC and R&D accruals/prepaids (CRO fees investigator fees lab fees and other vendor costs) a signficant plus.
Ability to work closely with other departments to ensure...
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Vollzeit
...Contribute to vendor evaluation and selection assist in contract preparation.
Responsible for vendor oversight and the initial review of CRO and other thirdparty study vendor invoices to ensure that work is performed in accordance with the scope of work.
Plan and support...
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Vollzeit
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Französischkenntnisse(88)
Temporär(64)
...relevant & significant clinical study experience: either from pharma/biotech leading early phase clinical trials; a senior role within a CRO responsible for leading the medical relationship with Sponsors; from a relevant academic medical center with PI & co-PI clinical...
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Novartis Pharma AG
Basel BS
Vor 29 Tagen
...sample analysis.
Role Requirements
• M.S. or Ph.D. with significant and relevant (10+ years) GCP experience in a pharmaceutical, CRO or related industry.
• Demonstrated experience leading a regulated biologics BA team. Preference to candidates with past experience...
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Vollzeit
Temporär
Schichtarbeit
...oversight and technical guidance of all analytical development in your projects
related activities for development projects performed at CRO/CMO site
selection and management of providers of analytical services
monitor analytical activities from starting material to...
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Vollzeit
...relevant & significant clinical study experience: either from pharma/biotech leading early phase clinical trials; a senior role within a CRO responsible for managing the medical relationship with Sponsors; from a relevant academic medical center with PI & co-PI clinical...
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Vollzeit
...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...
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Vollzeit
Postdoc Stelle
...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...
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Vollzeit
Lehrstelle
Flexible Arbeitszeit
