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Executive Global Study Associate Astrazeneca Jobs

Parexel

Local Study Associate Director- FSP

Reports study progress/update to the Global Study Associate Director/ Global Study Team including Site Management and Monitoring (SMM) Lead. * Contributes to patient recruitment strategy including ...

Parexel

Local Study Associate Director- FSP

Reports study progress/update to the Global Study Associate Director/ Global Study Team including Site Management and Monitoring (SMM) Lead. * Contributes to patient recruitment strategy including ...

IQVIA

Senior Global Clinical Study Manager

Tampa, FL

Required Experience * 2+ years of global study management experience * Experience across multiple ... Facilitate internal and external meetings, including executive presentations * Drive collaboration ...

IQVIA

Senior Global Clinical Study Manager

Tampa, FL

Required Experience * 2+ years of global study management experience * Experience across multiple ... Facilitate internal and external meetings, including executive presentations * Drive collaboration ...

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How much do executive global study associate astrazeneca jobs pay per year?

As of Aug 24, 2026, the average yearly pay for executive global study associate astrazeneca in the United States is $89,977.00, according to ZipRecruiter salary data. Most workers in this role earn between $55,500.00 and $132,500.00 per year, depending on experience, location, and employer.

What does an Executive Global Study Associate at AstraZeneca do?

An Executive Global Study Associate at AstraZeneca supports the planning, coordination, and execution of global clinical trials. They work closely with project managers, clinical teams, and external partners to ensure studies are conducted according to regulatory standards and company protocols. Their responsibilities include maintaining study documentation, managing timelines, tracking progress, and assisting with problem-solving throughout the study lifecycle. This role is essential for ensuring that clinical trials are delivered efficiently, compliantly, and on schedule.

How does an Executive Global Study Associate at AstraZeneca typically collaborate with cross-functional teams during a clinical trial?

As an Executive Global Study Associate at AstraZeneca, you will regularly collaborate with cross-functional teams including clinical operations, data management, regulatory affairs, and medical writing. Your role often involves coordinating meetings, ensuring timely communication between departments, and supporting the progress of study milestones. Effective collaboration is essential for resolving issues, aligning on study timelines, and maintaining compliance with regulatory standards. This teamwork fosters a dynamic environment where proactive communication and organizational skills are highly valued.

What are the key skills and qualifications needed to thrive as an Executive Global Study Associate at AstraZeneca, and why are they important?

To thrive as an Executive Global Study Associate at AstraZeneca, you need a solid background in clinical research, project management, and a relevant life sciences degree. Familiarity with clinical trial management systems (CTMS), regulatory documentation, and Good Clinical Practice (GCP) certification is typically required. Strong attention to detail, organizational skills, and effective cross-cultural communication are valuable soft skills in this role. These competencies ensure smooth coordination of global clinical trials, regulatory compliance, and successful collaboration across international teams.

What is the difference between Executive Global Study Associate Astrazeneca vs Clinical Research Associate Astrazeneca?

AspectExecutive Global Study Associate AstrazenecaClinical Research Associate Astrazeneca
CredentialsBachelor's degree, relevant certificationsBachelor's degree, clinical research certifications
Work EnvironmentGlobal study coordination, cross-functional teamsSite monitoring, patient interaction
Employer & Industry UsagePharmaceutical research, global trialsClinical trial management, site oversight

The Executive Global Study Associate Astrazeneca focuses on coordinating and supporting global clinical studies, often involving cross-functional teams and strategic planning. In contrast, the Clinical Research Associate Astrazeneca primarily monitors clinical trial sites and ensures compliance. Both roles require relevant degrees and certifications but differ in scope and daily responsibilities.

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Executive Global Study Associate Astrazeneca jobs near you
Infographic showing various Executive Global Study Associate Astrazeneca job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 28% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $89,977 per year, or $43.3 per hour.

Global Study Director

South San Francisco, CA • On-site

AstraZeneca GmbH
See more jobs at AstraZeneca GmbHexternal

$180 - $240/hr

Other

Posted 11 days ago

Job description

Introduction to role

Are you ready to lead the charge in groundbreaking clinical studies? As a Global Study Director (GSD), you will play a pivotal role in the Cell Therapy Clinical Operations organization, driving the operational planning and delivery of high-priority and complex clinical studies. Your expertise will ensure the successful execution of clinical trials, managing quality, timelines, budgets, resources, investigational sites, vendors, and key project deliverables. Leading a cross-functional study team, you will provide direction and guidance to achieve study milestones. Collaborate with internal and external stakeholders to resolve issues and ensure compliance with SOPs, regulatory requirements, and ICH/GCP guidelines. Your leadership will extend to mentoring GSADs and spearheading non-drug programs and improvement projects.

Accountabilities
  • - Lead and coordinate a cross-functional study team to ensure clinical study progress according to timelines, budget, and quality standards.
  • - Contribute to vendor/ESP selection activities and lead operational oversight at the study level.
  • - Assist with operational planning for upcoming clinical studies, interfacing with cross-functional partners.
  • - Collaborate to establish strategies for increasing efficiency of global study teams.
  • - Facilitate communication across functions and provide guidance to study team members.
  • - Serve as the primary AZ contact for outsourced studies, ensuring delivery according to agreed standards.
  • - Hold accountability for essential study level documents development.
  • - Ensure external service providers perform to contracted goals and timelines.
  • - Develop and maintain relevant study plans, including risk management planning.
  • - Oversee study level performance against plans, milestones, and KPIs.
  • - Identify and report quality issues within the study and collaborate to overcome barriers.
  • - Ensure Trial Master File completion and compliance with governance controls.
  • - Manage study budget through lifecycle and provide progress reports.
  • - Ensure studies are inspection-ready at all times.
  • - Support professional development of team members.
  • - Provide guidance and mentoring to less experienced colleagues.
  • - Lead non-drug project work and improvement projects.
Essential Skills/Experience
  • - University degree or equivalent in medical or biological sciences or discipline associated with clinical research.
  • - Proven project management experience and training.
  • - At least 7 years of clinical trial experience.
  • - At least 3 years of experience in global study leadership and team leadership.
  • - Demonstrated clinical trial expertise in hematology and/or oncology.
  • - Extensive knowledge of ICH-GCP guidelines and clinical research regulatory requirements.
  • - Thorough understanding of the cross-functional clinical trial process.
  • - Strong strategic and critical thinking abilities.
  • - Proven skills in complex problem solving and decision-making.
  • - Strong abilities in establishing effective working relationships with senior stakeholders.
  • - Demonstrated abilities in mentoring.
  • - Excellent communication and interpersonal skills.
  • - Ability to manage multiple competing priorities.
  • - Experience in external provider oversight and management.
Desirable Skills/Experience
  • - Advanced degree, masters level education or higher.
  • - Project management certification.
  • - 5 years of experience in global study leadership and team leadership.
  • - Significant hematology/oncology expertise.
  • - Expertise in different phases of clinical delivery.
  • - Experience with project management software solutions.
    • - Cell therapy/CAR-T experience.
    • - Global phase 3 study experience.
Date Posted

10-Aug-2026

Closing Date

30-Aug-2026

Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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