Early Development Project Leader
Accountable for the key deliverables of the drug early development and pre-clinical project and lead a multidisciplinary team
January 17, 2022
INSIGHTS
Global Program Head Anti-Infectives
Guide innovation, provide drug development expertise and strategic leadership to the Programs and project teams, comprising all pre-clinical, clinical, technical, regulatory, operational and commercial disciplines
January 9, 2022
Clinical Safety Physician, Early Drug Development
Monitor and report on the progress of delegated clinical trials, which includes budgets and timelines. Prepare, oversee, and review documents that are related to assigned clinical study.
December 8, 2021
Scientist, Clinical Pharmacology and Pharmacometrics
Monitor and report on the progress of delegated clinical trials, which includes budgets and timelines. Prepare, oversee, and review documents that are related to assigned clinical study.
December 2, 2021
Associate Principal Scientist Clinical Pharmacology
Monitor and report on the progress of delegated clinical trials, which includes budgets and timelines. Prepare, oversee, and review documents that are related to assigned clinical study.
December 2, 2021
Senior Scientist, Nonclinical DMPK
Monitor and report on the progress of delegated clinical trials, which includes budgets and timelines. Prepare, oversee, and review documents that are related to assigned clinical study.
December 2, 2021
Monitor and report on the progress of delegated clinical trials, which includes budgets and timelines. Prepare, oversee, and review documents that are related to assigned clinical study.
November 29, 2021
Monitor and report on the progress of delegated clinical trials, which includes budgets and timelines. Prepare, oversee, and review documents that are related to assigned clinical study.
October 19, 2021
Principal Scientist Pharmacology & Screening Anti-infectives
Be an integral member of the clinical development team and the clinical study team and drive execution of the clinical study in partnership with other functions
September 18, 2021
Author and review clinical and regulatory documents such as Study Protocols, ICFs, CSRs, IBs, Paediatric Investigation Plans, Briefing Books, Requests of Product Specific Waivers, applications for Orphan Drug Designations, and responses to Health Authorities; the documents should be accurate, suited for the intended audience and easy to read.
July 24, 2021
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Contact information
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- (+41) 78 889 3675
- signe.reidla@execruits.com