Global Study Manager
Global Study Manager
Posted on :
25-04-2024
Employer Active
1 Vacancy
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Job Description
Req ID : 2754060
- Accountabilities:
As a Global Study Manager, you'll contribute to the development of study documents, lead the preparation of country-specific agreements, manage third-party vendors, provide input to data management documents, and oversee the supply of Investigational product and study materials. You'll also monitor study conduct and progress, support risk management and quality efforts, prepare presentation material for meetings, and contribute to the implementation of audits and regulatory inspections.
Essential Skills/Experience:
- Bachelor's Degree and 3+ years of experience, Associate's degree plus 7+ years of experience or High School plus 11+ years of experience
- Experience of working with and delivering through strategic partners and 3rd party vendors
- Excellent knowledge of ICH-GCP principles
- Team orientated
- Ability to coordinate and prioritize multiple tasks and deliverables
- Proactive approach
- High degree of flexibility
- Demonstrated verbal and written communication skills
- Good negotiation and collaboration skills
- Demonstrated interpersonal and problem-solving skills
- Some travel may be required
- Desirable Skills/Experience:
- Early phase oncology clinical trial experience
- Global study management experience
- When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines.
- In-person working gives us the platform we need to connect,
- work at pace and challenge perceptions. That’s why we work, on average, a minimum of three days per week from the office.
- But that doesn't mean we’re not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.
Employment Type
Full Time
Department / Functional Area
Key Skills
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