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ADME Pharmacokinetic Study Manager(m/w/x)
Managing outsourced in vitro/in vivo ADME/PK studies at a global pharmaceutical company, utilizing automated request and tracking systems. Proven project/study management experience in drug discovery/DMPK and outsourced studies required. Influence development of automated study tracking and data management tools.
Requirements
- University degree (BSc, MSc, or PhD) in Life Sciences, Pharmacology, Biochemistry, or related field
- Proven project or study management experience within drug discovery, DMPK, or related R&D functions
- Experience managing outsourced studies and external research partnerships (CROs)
- Interest and capability to collaborate with technical experts in developing and maintaining study tracking or data management tools
- Strong interpersonal and communication skills with a collaborative, solution-oriented mindset
- Ability to manage multiple projects and priorities effectively while maintaining attention to detail
Tasks
- Manage outsourced in vitro and in vivo studies
- Coordinate automated study requests and tracking
- Support outsourcing of ADME screening assays and PK studies
- Ensure operational efficiency and timely data delivery
- Utilize automated study request systems and tracking workflows
- Collaborate with scientific experts and project teams
- Partner with contract research organizations (CROs) to optimize assay performance
- Develop and maintain study tracking tools
- Contribute to process automation initiatives for data visibility
- Communicate study progress, timelines, and outcomes to stakeholders
- Foster a collaborative environment in screening operations
- Contribute to continuous improvement in partner management
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
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ADME Pharmacokinetic Study Manager(m/w/x)
Managing outsourced in vitro/in vivo ADME/PK studies at a global pharmaceutical company, utilizing automated request and tracking systems. Proven project/study management experience in drug discovery/DMPK and outsourced studies required. Influence development of automated study tracking and data management tools.
Requirements
- University degree (BSc, MSc, or PhD) in Life Sciences, Pharmacology, Biochemistry, or related field
- Proven project or study management experience within drug discovery, DMPK, or related R&D functions
- Experience managing outsourced studies and external research partnerships (CROs)
- Interest and capability to collaborate with technical experts in developing and maintaining study tracking or data management tools
- Strong interpersonal and communication skills with a collaborative, solution-oriented mindset
- Ability to manage multiple projects and priorities effectively while maintaining attention to detail
Tasks
- Manage outsourced in vitro and in vivo studies
- Coordinate automated study requests and tracking
- Support outsourcing of ADME screening assays and PK studies
- Ensure operational efficiency and timely data delivery
- Utilize automated study request systems and tracking workflows
- Collaborate with scientific experts and project teams
- Partner with contract research organizations (CROs) to optimize assay performance
- Develop and maintain study tracking tools
- Contribute to process automation initiatives for data visibility
- Communicate study progress, timelines, and outcomes to stakeholders
- Foster a collaborative environment in screening operations
- Contribute to continuous improvement in partner management
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
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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