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Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Deliver study execution by providing operational expertise into protocol design and feasibility, country selection, patient centricity and data delivery plans
- Ensure study quality and integrity by developing and maintaining study systems and documentation
- Provide country oversight for insourced studies
- Manage vendor performance by providing direction and actively managing relationships
- Plan demand and supply by overseeing the forecasting and maintenance of supplies needed for clinical studies
- Manage risk and compliance by assisting the study team in identifying, managing and mitigating study-related risks
- Drive operational excellence by providing operational expertise across operations-related activities
Requirements
What you’ll need- Hold a university degree or equivalent years of experience (preferred focus in life sciences)
- Strong and consistent performance as a Study Manager or equivalent in pharmaceutical and/or healthcare industry
- Drug development experience (therapeutic area experience a plus)
- Strong working knowledge of drug development process and respective regulations, including ICH and GCP guidelines
- Able to think on your feet and thrive in fast-paced, ambiguous and highly collaborative environments
Benefits
Comp & perks- 1-year fixed-term contract
- Opportunity to work in a collaborative, patient-centric environment
- Scientific rigor and innovation in drug development
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
Protocol DesignFeasibility AssessmentData Delivery PlanningRisk ManagementSupply ForecastingStudy DocumentationOperational Expertise
Soft Skills
CollaborationProblem SolvingAdaptability
