Clinical Trial Manager Jobs in Basel
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Search Results - Clinical Trial Manager Jobs in Basel
StudySmarter GmbH-Basel-appcast.io-
Apsida Life Science has partnered with a leading biopharmaceutical client to identify a Sr. Global Strategic Manager for Allschwil, Switzerland. This full-time role focuses on strategic sourcing leadership for late-stage clinical trials, ESP...
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IQVIA-Basel-stellen-basel.ch-
Clinical Independent Rater – Turkish Speaking
Location: Remote/Virtual
Hours: Estimated 10–16 hours per month
Role: Clinical Independent Rater for Clinical Trials
About IQVIA
IQVIA is a global leader in advanced analytics, technology solutions...
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StudySmarter GmbH-Basel-appcast.io-
independent sourcing subject matter expertise to study teams
• Partner with study teams, functional areas and ESPs in forecasting/managing clinical deliverables and maintain collaborative relationships.
• Demonstrated ability to perform reviews of the scope...
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Research-Basel-stellen-basel.ch-
publications and professional contributions.
• Broad knowledge of oncology drug development and clinical trial execution.
• Excellent written and verbal communication skills.
• Proven leadership and people management experience.
• Strong mentoring...
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IQVIA LLC-Basel-appcast.io-
IQVIA LLC seeks a Systems Design Project Manager for IRT Basil, Switzerland, to design and deliver IRT systems for clinical trials. You will work with sponsors to translate study requirements into system specs, oversee implementation, and manage...
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IQVIA-Basel-stellen-basel.ch-
Clinical Trial Psych Rater – Hungarian Speaking
Location: Remote/Virtual
Hours: Estimated 10–16 hours per month
Role: Clinical Specialist
About IQVIA
IQVIA is a global leader in advanced analytics, technology solutions, and clinical research...
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BeiGene, Ltd.-Basel-appcast.io-
a thorough understanding of global regulatory requirements and guidelines governing the conduct of clinical trial operations across multiple regions.
Supervisory Responsibilities:
Not Applicable
Computer Skills:
All basic Microsoft Office Programs
Other...
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Roche-Basel-roche.com-
with tailored learning solutions, making it an ideal entry-point for aspiring regulatory professionals. Participants gain invaluable insights into the complete lifecycle of pharmaceutical products, from initial clinical trials to market exit, by engaging...
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IQVIA LLC-Basel-appcast.io-
Systems Design Project Manager – IRT Basil, Switzerland
About the Role
The Systems Design Project Manager (IRT) plays a key role in supporting clinical trials by designing and delivering IRT systems that ensure patients receive the correct study...
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IQVIA-Basel-stellen-basel.ch-
Clinical Trial Psych Rater – German Speaking
Location: Remote/Virtual
Hours: Estimated 10–16 hours per month
Role: Clinical Specialist
About IQVIA
IQVIA is a global leader in advanced analytics, technology solutions, and clinical research...
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Roche-Basel-roche.com-
processes and the highest scientific standards—utilising deliverables based on advanced data science, pharmacoepidemiology methodologies, and literature queries across Real World Data, Clinical Trial data, and literature databases while staying abreast...
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Roche Holding AG-Basel-stellen-basel.ch-
medicines to life. In this strategic leadership role, you will lead Technical Development Teams (TDTs) to design and drive Chemistry, Manufacturing, and Control (CMC) strategies for clinical drug candidates for synthetic molecules. From early human trials...
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Roche-Basel-roche.com-
independently develop, validate, and maintain datasets and statistical outputs for clinical trials, including Study Data Tabulation Model (SDTM) datasets, Analysis Data Model (ADaM) datasets, and tables, listings, and figures (TLFs), ensuring programming...
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IQVIA-Basel-stellen-basel.ch-
Systems Design Project Manager – IRT
Basil, Switzerland
About the Role
The Systems Design Project Manager (IRT) plays a key role in supporting clinical trials by designing and delivering IRT systems that ensure patients receive the correct study...
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ten23 health AG-Basel-stellen-basel.ch-
to the transfer of manufacturing processes from the client to the CDMO facility.
Day-to-Day Tasks
• Reviewing a new SOW for a client's phase III clinical trial drug product batch filling to ensure the timelines, pricing, and liabilities match the master...
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