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ADME Pharmacokinetic Study Manager(m/w/x)
Description
As an ADME Pharmacokinetic Study Manager, you will oversee the management of outsourced studies, ensuring efficient operations and timely data delivery. You will collaborate with internal experts and external partners to enhance scientific excellence.
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Upload your CV and Nejo AI will find matching job offers for you.
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
Education
Work Experience
approx. 1 - 4 years
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
Languages
English – Business Fluent
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ADME Pharmacokinetic Study Manager(m/w/x)
The AI Job Search Engine
Description
As an ADME Pharmacokinetic Study Manager, you will oversee the management of outsourced studies, ensuring efficient operations and timely data delivery. You will collaborate with internal experts and external partners to enhance scientific excellence.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
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
Education
Work Experience
approx. 1 - 4 years
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
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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