Clinical Trial Manager Jobs in Basel
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Search Results - Clinical Trial Manager Jobs in Basel
Proclinical StaffingBasel
the clinical supply chain. In this role, you will develop and implement optimal clinical trial supply strategies, ensuring continuity of supply to patients while managing risks effectively. This position offers an opportunity to work on a diverse portfolio...
Novartis AGBaseljobup.ch
Responsibilities:
• Operationally and scientifically lead complex clinical studies
• Drive and deliver aspects of global clinical trial execution from study design, set-up and recruitment to final reporting
• Lead the matrix-management of robust global clinical...
Stiftung WeizenkornBasel
Stiftung Weizenkorn is looking for a Clinical Trial Supply Manager for a global project in Basel, Switzerland. The successful candidate will define and execute clinical trial supply strategies, ensuring timely delivery of materials to patients...
Bayer Consumer Care AGBasel
and other COA assessments for clinical programs. Your mission is to enhance the patient experience from trial design to final reporting, ensuring commercial and regulatory success of products that include COAs in their endpoint measurement strategy across...
Novartis FarmacéuticaBasel
are maintained throughout the clinical trial lifecycle.
The ideal candidate will have at least 2 years of experience in clinical trial management and strong leadership skills. A commitment to mentor junior team members and optimize trial operations is essential...
Bayer Consumer Care AGBasel
of brilliant and diverse minds to make a real difference, there's only one choice.
Senior HEOR Manager Patient-Reported Outcome (12 months contract) m/f/d
As a Senior HEOR Manager COAs/PROs, you are at the forefront of clinical outcome assessment (COA)...
ITJOBSBasel
Biomarker, PK and PD) across the portfolio of trials. The BOL is an integral part of the Clinical Trial Team and provides operational/ project management expertise as it relates to sampling, site and patient logistics, and vendor management to ensure...
F. Hoffmann-La Roche GruppeBaselappcast.io
manager status
• Closely interface with project team leaders as well as safety, clinical pharmacology, clinical operations, biostatistics, regulatory, research and biomarker groups and other members of project teams
• Lead and/or support internal...
Baselicims.com
Overview:
The Manager, GMP Quality is responsible for the oversight and day-to-day quality interface with CDMO producing DS & DP for MRTx's ongoing clinical programs.. This includes supporting the review of MBRs/EBRs, analytical methods...
F. Hoffmann-La Roche AGBaselappcast.io
Scientists in a line‑ or functional‑manager capacity.
• Interface closely with project team leaders and cross‑functional groups including safety, clinical pharmacology, clinical operations, biostatistics, regulatory, research, and biomarker teams.
• Manage...
Revolution MedicinesBasel
across early‑ and late‑stage CMC regulatory activities, including clinical trial applications, initial marketing authorization applications (MAA), post‑approval variations, and lifecycle strategy.
The position requires deep expertise in EU regulatory...
F. Hoffmann-La Roche GruppeBaselappcast.io
functional teams on study analytics, data management, and safety profiles.
• Scientific Leadership: Maintain the highest levels of scientific and clinical knowledge within the MS and Neuroimmunology therapeutic areas.
• Regulatory Engagement: Take an active...
Monte Rosa Therapeutics Inc.Basel
Overview
In this exciting role the successful candidate will contribute to CMC tasks from discovery/preclinical stage to clinical and potentially commercial stage. This includes managing outsourcing activities for development and manufacturing...
Stiftung WeizenkornBaselappcast.io
times per week, participate in clinical rounds and journal clubs, and contribute to patient management decisions at a consultant level
• Engage in clinical research within the Cardiovascular Research Institute Basel (CRIB). Fellows will receive...
Abbott LaboratoriesBaselappcast.io
Act as a core member of the Product Safety Team, overseeing medical safety monitoring and contributing to PSURs, clinical overviews, and risk‑management plans
• As part of the Labeling Sub‑Team, provide medical input and scientific strategies...
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