Clinical Trial Manager Jobs
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Universität Zürich-Zurich
complete and audit-ready documentation.
• Establishing and continuously improving study processes, SOPs and quality systems, including the management of monitoring visits, audits, inspections, deviations and corrective actions.
• Managing the clinical trial...
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Bayer Consumer Care AG-Basel
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 clinical lifecycles.
YOUR...
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Debiopharm-Lausanne
Lausanne, Switzerland
Your Mission:
As the Senior Manager of Statistical Programming, you will provide strategic leadership for Statistical and Clinical Data Science Programming. You will be the driving force behind our digitalization strategy...
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Bayer Consumer Care AG-Basel
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)...
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Rivia SA-Zurich
Rivia is a technology company building a data engine that powers the future of clinical trial intelligence. Rivia was founded on the belief that new drugs can be brought to market more successfully with a fraction of today's capital.
Biotechs...
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ITech Consult AG-Basel
By joining us, you step into an innovative environment where we build cutting-edge tools, automation, and next-generation technologies that streamline clinical trial data collection and delivery, accelerating the release of life-saving medicines to patients...
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Cpl Life Sciences-St. Gallen
and commercialisation.
• Experience preparing and reviewing regulatory submissions including:
• Clinical Trial Applications (CTAs)
• Marketing Authorisation Applications (MAAs)
• Variations and lifecycle management submissions
• Experience interpreting and applying...
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EPFL-Lausanne
public health, or a related field.
• Significant experience managing human biological samples, human subjects/clinical research data and clinical trials.
• Demonstrated experience in research infrastructure leadership, biobanking governance, data...
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Elan Personal AG-Basel
lead the industry in speed, quality, and efficiency. By joining Roche, the individual will become part of an innovative environment where cutting-edge tools, automation, and next-generation technologies are developed to streamline clinical trial data...
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ITech Consult AG-Basel
pipeline, supporting research, early development, and clinical trials through technical innovation and collaboration. This position is located within the Analytical Development for Synthetic Molecules department, where cutting-edge techniques such as High...
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Gi Life Sciences Basel-Basel
pharmaceutical ingredients (APIs), drug products, and analytical sciences. PTDC plays a vital role in advancing the synthetic molecules pipeline, supporting research, early development, and clinical trials through technical innovation and collaboration...
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Idorsia-Allschwil
Manager (Artwork Focus) to join our Commercial Packaging & Clinical Trial Supply Team !
Job Responsibilities
• Lead and manage commercial pharmaceutical artwork projects across the product lifecycle, ensuring timely delivery, quality, compliance...
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two.jobs-Bern
to improving cancer treatment for the Swiss population as a non-profit organization. Guided by our vision “Clinical research for a cure tomorrow,” we conduct oncology clinical trials and serve as a key partner for authorities, professional associations...
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Roche-Kaiseraugst
and extensive years of professional experience.
• You have a strong understanding of end-to-end supply chain management, including warehouse and transportation management, logistics, and regulatory requirements for clinical trials.
• You bring relevant GXP...
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Travere Therapeutics-Schweiz
in the preparation, submission and maintenance of regulatory applications, including clinical trial applications (CTA), routine CTA amendments, pre & post authorization regulatory submissions and annual reports.
• Support regulatory leads in the preparation, review...
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