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Study Project Manager I(m/w/x)
Leading clinical research studies from initiation to completion for innovative medicines. 6 years pharma/clinical research experience required. Medical device trial experience a plus.
Requirements
- Bachelor’s Degree or equivalent degree
- 6 years pharma/clinical research experience
- Exposure in study initiation to completion (Phase 1-4)
- Medical Device Trial Experience
Tasks
- Drive connection between science and operational delivery
- Ensure operational excellence in clinical research studies
- Execute studies with quality, efficiency, and on-time
- Bring scientific acumen and strategic thinking to address risks
- Lead cross-functional Clinical Study Teams
- Define and drive operational strategies and deliverables
- Ensure compliance with quality standards (ICH/GCP, Global Regulations, AbbVie policies)
- Manage budget, timelines, and study issues proactively
- Influence cross-functional stakeholders to achieve milestones
- Manage vendors and external stakeholders effectively
- Foster a growth mindset and continuous learning
- Coach and support cross-functional team members
- Contribute to operational efficiencies and innovation
- Demonstrate excellent communication and problem-solving skills
- Prioritize patient and customer needs
- Navigate ambiguity and thrive in uncertain situations
- Develop clinical study design and associated systems
- Create and oversee study budgets
- Select, manage, and oversee external vendors
- Identify and address study-related risks and issues
- Empower decision-making in study execution
- Create an inclusive and innovative environment
- Lead, delegate, and support Study Management Associates
Work Experience
- 6 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
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Study Project Manager I(m/w/x)
Leading clinical research studies from initiation to completion for innovative medicines. 6 years pharma/clinical research experience required. Medical device trial experience a plus.
Requirements
- Bachelor’s Degree or equivalent degree
- 6 years pharma/clinical research experience
- Exposure in study initiation to completion (Phase 1-4)
- Medical Device Trial Experience
Tasks
- Drive connection between science and operational delivery
- Ensure operational excellence in clinical research studies
- Execute studies with quality, efficiency, and on-time
- Bring scientific acumen and strategic thinking to address risks
- Lead cross-functional Clinical Study Teams
- Define and drive operational strategies and deliverables
- Ensure compliance with quality standards (ICH/GCP, Global Regulations, AbbVie policies)
- Manage budget, timelines, and study issues proactively
- Influence cross-functional stakeholders to achieve milestones
- Manage vendors and external stakeholders effectively
- Foster a growth mindset and continuous learning
- Coach and support cross-functional team members
- Contribute to operational efficiencies and innovation
- Demonstrate excellent communication and problem-solving skills
- Prioritize patient and customer needs
- Navigate ambiguity and thrive in uncertain situations
- Develop clinical study design and associated systems
- Create and oversee study budgets
- Select, manage, and oversee external vendors
- Identify and address study-related risks and issues
- Empower decision-making in study execution
- Create an inclusive and innovative environment
- Lead, delegate, and support Study Management Associates
Work Experience
- 6 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
AbbVie
Industry
Pharmaceuticals
Description
Das Unternehmen setzt sich für die Entdeckung und Bereitstellung innovativer Medikamente und Lösungen ein, die ernsthafte Gesundheitsprobleme lösen.
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