Clinical Trial Manager Jobs in Lausanne
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Suchergebnisse - Clinical Trial Manager Jobs in Lausanne
Interim Legal-Lausanne
Legal Counsel, Clinical Trials (Life Sciences Company)
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Legal Counsel, Clinical Trials (Life Sciences Company)
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Interim Legal
Legal Counsel, Clinical Trials (Life Sciences Company)
3 days ago Be among the first 25...
Debiopharm-Lausanne
stakeholders in vendor qualification, study risk management, team training, and quality coaching while monitoring key risk indicators and trends. Your expertise will help uphold the integrity of clinical trial data, safeguard patient safety, and drive...
Debiopharm-Lausanne
reporting for clinical trials under the supervision of the Clinical Safety Manager.
• Participate in multidisciplinary study team meetings alongside Clinical Safety Officers.
• Collaborate with internal teams, vendors, CROs, and partners to execute CS&PV...
workable.com -
Philip Morris International-Lausanne
including clinical trial, research collaboration, license, distribution, and vendor contracts, while mitigating risks and balancing business interests.
Partners with internal clients to support projects in particular coming from PMI’s scientific activities...
Debiopharm-Lausanne
development projects—including small molecules, biologics (ADCs), and radiopharmaceuticals. You’ll be the cornerstone for delivering high-quality CMC documentation to support clinical trial applications (Phase 1 to Phase 3), due diligences, and licensing...
appcast.io -
Debiopharm-Lausanne
Management organization in Lausanne, we are looking for a
Clinical Development Quality Team Lead ( 100%)
As a hands-on Clinical Development Quality Team Lead, you will lead the Clinical Development Quality Team driving compliance to the DPIs Quality...
workable.com -
Debiopharm-Lausanne
documentation for clinical trial applications, supporting Regulatory Affairs.
• Act as the key contact for CDMOs/CROs: oversee activities, challenge proposals, ensure scientific/documentary compliance.
• Collaborate in CMC strategy development, contributing...
appcast.io -
Debiopharm-Lausanne
stakeholders in vendor qualification, study risk management, team training, and quality coaching while monitoring key risk indicators and trends. Your expertise will help uphold the integrity of clinical trial data, safeguard patient safety, and drive...
Debiopharm-Lausanne
documentation for clinical trial applications, supporting Regulatory Affairs.
• Act as the key contact for CDMOs/CROs: oversee activities, challenge proposals, ensure scientific/documentary compliance.
• Collaborate in CMC strategy development, contributing...
workable.com -
Voisinconsulting-Lausanne
of standardized, reusable outputs and templates to support multiple studies
Collaborative and Communication Skills
Comfortable working cross-functionally with statisticians, data managers, and clinical teams
Strong documentation practices and the ability...
Debiopharm-Lausanne
This internship is your chance to dive into exciting statistical challenges such as dose optimization, adaptive phase 2/3 seamless designs, and probability of success of clinical trials.
Your Mission.
• Be part of a Clinical Trial Team and support study-level...
workable.com -
Debiopharm-Lausanne
development projects—including small molecules, biologics (ADCs), and radiopharmaceuticals. You’ll be the cornerstone for delivering high-quality CMC documentation to support clinical trial applications (Phase 1 to Phase 3), due diligences, and licensing...
workable.com -
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