Clinical Trial Manager Jobs
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Suchergebnisse - Clinical Trial Manager Jobs
Roche Holding AG-Basel
in the pharmaceutical/healthcare industry and drug development (therapeutic area a plus), alongside a solid understanding of the clinical trial environment, ICH‑GCP, and lifecycle sequence/interdependencies.
• You are highly experienced in clinical trial management...
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AXEPTA SA-Genf
of evidence: IFU, risk management files, PMS data, trials and tests, labelling, complaints, vigilance and scientific literature.
• Ensure the alignment of clinical data within all regulatory documentation.
• Train and support the external providers involved...
Debiopharm-Lausanne
Mission
The Clinical Development Quality Manager (CDQM) is responsible for ensuring quality oversight across clinical development activities and supporting the maintenance of GCP compliance. This role supports stakeholders in vendor qualification...
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SJP Biotec GmbH-Zürich
development field - RAS/eIF4A/translation-pathway inhibition.
Key Responsibilities
Translate and deliver key directives from the board and senior management, and serve as the clinical face of the company.
Lead and manage all clinical development activities...
BeiGene, Ltd.-Basel
RCC) Inspection Lead is responsible for driving proactive risk management, sustained inspection readiness, audit support, and regulatory compliance across clinical trials. The role provides leadership and oversight to ensure consistent implementation...
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SJP Biotec GmbH-Zürich
Key Responsibilities
• Translate and deliver key directives from the board and senior management, and serve as the clinical face of the company.
• Lead and manage all clinical development activities across the SJP portfolio
• Design Phase 2 and 3...
AXEPTA SA-Genf
in charge of writing clinical documents.- Verify the consistency of the different sources of evidence: IFU, risk management files, PMS data, trials and tests, labeling, vigilance, and scientific literature.- Ensure the alignment of clinical data within...
Neurocrine Biosciences-Allschwil
to multidisciplinary project teams for assigned TA/Program, advises Senior Technical Leadership and Executive Management and regularly interfaces with internal and external colleagues to ensure timely and accurate dissemination of Clinical Pharmacology findings.
Your...
Roche-Basel
understanding of the clinical trial environment, ICH-GCP, and lifecycle sequence/interdependencies.
• You are highly experienced in clinical trial management tools, systems, and their interdependencies, specifically including IxRS, eCOA, centralised endpoint...
roche.com -
Rivia SA-Zürich
About Rivia Rivia is a data engine for clinical trial intelligence. It provides data infrastructure and AI-driven workflows for clinical trial teams, enabling biotechs to run studies more efficiently and to demonstrate which patients derive...
Alentis Therapeutics-Allschwil
management:
• Develop demand forecasts and supply plans based on study protocols, clinical scenarios and enrollment projections.
• Plan, implement and execute the supply strategy for trial medication and ancillary supplies in collaboration with clinical...
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Swiss Cancer Institute-Bern
research for a cure tomorrow," we conduct oncology clinical trials and serve as a key partner for authorities, professional associations, and the pharmaceutical industry. Approximately 70 employees at our Competence Center in Bern work closely with all...
Universitätsspital Zürich USZ-Zürich
and laboratory teams to jointly define research questions, develop analytical strategies, and execute research projects
• Additionally, you will contribute to prospective clinical studies and treatment trials in patients with sarcoidosis and apply advanced data...
Roche-Basel
development plans from Phase 1 through Phase 2 (proof-of-concept)
• Coach Clinical Scientists in a line- or functional-manager status
• Closely interface with project team leaders as well as safety, clinical pharmacology, clinical operations, biostatistics...
Johnson & Johnson Innovative Medicine-Allschwil
documents, including:
Risk management plans.
Safety development plan.
Clinical Trial Protocols and Informed Consent Forms (ICF).
Safety sections of Investigator's Brochure (IB) and addenda.
Clinical Study Reports (CSR).
Annual Safety Reports (ASR...
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