Astrazeneca

Healthcare

GlobalStudyManager

$0–0k Gaithersburg, Maryland, United States FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Manager candidates.

The Brief

“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.

Healthcare
Problems you'll solve

Problem-solving skills

Eligibility Requirements

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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