Astrazeneca
Healthcare
GlobalStudyManager
Neural analysis suggests this role is
optimal for Manager candidates.
“Global Study Manager at Astrazeneca. Skills: Study management, Vendor management, ICH-GCP principles. Support delivery of cell therapy clinical studies. Ensure quality and compliance”
Industry & Context.
Problem-solving skills
Some travel may be required
What They're Looking For.
Must Have
Bachelor's degree, 4+ years study manager experience, Experience with strategic partners, Experience with 3rd party vendors, Knowledge of ICH-GCP principles, Ability to lead tasks, Ability to coordinate tasks, Ability to prioritize tasks, Vendor Management experience, Proactive approach, Demonstrated verbal communication skills, Demonstrated written communication skills, Good negotiation skills, Good collaboration skills, Demonstrated interpersonal skills, Demonstrated problem-solving skills, Ability to manage change, High degree of flexibility
Nice to Have
Early phase oncology clinical trial experience, Late phase oncology clinical trial experience, Experience in autologous therapies, Experience in allogeneic therapies, Clinical Study Management experience
What You'll Do.
Support delivery of cell therapy clinical studies
Ensure quality and compliance
Contribute to development of study documents
Lead preparation of country-specific agreements
Manage third-party vendors
Provide input to data management documents
Ensure supply of study materials
Oversee third-party vendors
Oversee global internal staff
Oversee local internal staff
Oversee investigator sites
Support effective delivery of study
Monitor study conduct
Monitor study progress
Support risk management
Support quality efforts
Assist in implementation of audits
Assist in implementation of regulatory inspections
How You'll Work.
Team & Collaboration
Global internal staff; Local internal staff; Investigator sites
Communication Scope
Verbal communication; Written communication
Process & Methodology
Study management
Full Job Description
Are you ready to make a bold move in your career? Join us as a Global Study Manager in Cell Therapy, where you will be responsible for supporting the delivery of cell therapy clinical studies ensuring quality and compliance. This role requires a high degree of flexibility as the exact accountabilities will differ depending on the nature of the clinical program or study. As a Global Study Manager, you will 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 ensure the supply of study materials. You will also oversee third-party vendors, global / local internal staff, and investigator sites to support effective delivery of a study. Your role will involve monitoring study conduct and progress, support risk management and quality efforts, and assisting in the implementation of audits and regulatory inspections. You will be based in Gaithersburg, MD and will report to the Director, Study Management Cell Therapy. ## **Essential Qualifications: ** * Bachelor’s degree with 4+ years of experience as a study manager * Experience of working with and delivering through strategic partners and 3rd party vendors * Excellent knowledge of ICH-GCP principles * Ability to lead, coordinate and prioritize multiple tasks and deliverables * Vendor Management experience * Proactive approach to achieving study goals * Demonstrated verbal and written communication skills * Good negotiation and collaboration skills * Demonstrated interpersonal and problem-solving skills * Ability to manage change with a high degree of flexibility * Some travel may be required ## **Desirable Experience:** * Early/late phase oncology clinical trial experience * Experience in autologous or allogeneic therapies * Clinical Study Management experience #CellTherapy _The annual base pay for this position ranges from $112K to $168K. Our positions offer eligibility for various incentives—an opp
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