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Clinical Scientist immunology(m/w/x)
Clinical protocol finalization and scientific expertise for global Phase I-II studies, preparing reports for Health Authorities. PhD, MD, or MD/PhD, plus 5+ years clinical research experience in pharma required. International project collaboration.
Requirements
- PhD, MD, or MD/PhD (or equivalent qualification)
- Over five years (5+) of hands-on clinical research experience in the pharmaceutical industry
- Proven ability to rapidly grasp and become proficient in new indications
- Exceptional skills in evaluating, interpreting, and synthesizing complex scientific data
- Outstanding verbal and written communication skills in English
- true international perspective and strong track record as a team player
Tasks
- Drive the creation and finalization of clinical protocols
- Prepare clinical reports and Investigator Brochures
- Submit documents to Health Authorities
- Provide scientific expertise for global Phase I-II studies
- Ensure execution aligns with strategy, budget, and timelines
- Lead the medical-scientific review of clinical trial data
- Analyze and interpret clinical trial results
- Publish findings and create internal/external presentations
- Direct the global, cross-functional Study Management Team
- Ensure all deliverables meet strict quality standards
Work Experience
- 5 years
Education
- Doctoral / PhD
Languages
- English – Business Fluent
Not a perfect match?
- RocheFull-timeOn-siteSeniorBasel
- Roche
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Clinical Scientist immunology(m/w/x)
Clinical protocol finalization and scientific expertise for global Phase I-II studies, preparing reports for Health Authorities. PhD, MD, or MD/PhD, plus 5+ years clinical research experience in pharma required. International project collaboration.
Requirements
- PhD, MD, or MD/PhD (or equivalent qualification)
- Over five years (5+) of hands-on clinical research experience in the pharmaceutical industry
- Proven ability to rapidly grasp and become proficient in new indications
- Exceptional skills in evaluating, interpreting, and synthesizing complex scientific data
- Outstanding verbal and written communication skills in English
- true international perspective and strong track record as a team player
Tasks
- Drive the creation and finalization of clinical protocols
- Prepare clinical reports and Investigator Brochures
- Submit documents to Health Authorities
- Provide scientific expertise for global Phase I-II studies
- Ensure execution aligns with strategy, budget, and timelines
- Lead the medical-scientific review of clinical trial data
- Analyze and interpret clinical trial results
- Publish findings and create internal/external presentations
- Direct the global, cross-functional Study Management Team
- Ensure all deliverables meet strict quality standards
Work Experience
- 5 years
Education
- Doctoral / PhD
Languages
- English – Business Fluent
About the Company
1201 F. Hoffmann-La Roche AG
Industry
Pharmaceuticals
Description
Roche is dedicated to advancing science and ensuring access to healthcare for everyone, with over 100,000 employees globally.
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