Global Study Director – Clinical Operations

Astrazeneca AB; Göteborgs kommun, Mölndals kommun; On-site; SEK 1,000,000 - 1,300,000; Full time

Job summary

AstraZeneca AB in Gothenburg, Sweden, invites applications for a Global Study Associate Director to lead a cross-functional study team, ensure timely, high-quality delivery of clinical studies in CVRM, and act as main liaison between study teams and the Clinical Program Team.

You will develop study level documents, oversee external partners, ensure systems are current, and drive performance against plans and KPIs, including budget re-forecasts throughout the study lifecycle.

Qualifications

• Degree in medical or biological sciences or related field.
• Experience delivering clinical studies.
• Extensive study management experience.
• Solid knowledge of ICH-GCP and regulatory requirements.
• Strong leadership and communication.
• Ability to manage competing priorities.
• Experience with global studies.

Responsibilities

• Lead and guide a cross-functional study team.
• Develop essential study level documents.
• Oversee external service providers.
• Ensure study systems are current.
• Monitor performance against plans, milestones, and KPIs.
• Manage study budget re-forecasting.

Skills

Study management

Cross-functional leadership

Project management

ICH-GCP knowledge

Communication skills

Stakeholder management

Prior pharma experience

Education

University degree

Advanced degree desirable

Job description

AstraZeneca AB in Gothenburg, Sweden, invites applications for a Global Study Associate Director to lead a cross-functional study team, ensure timely, high-quality delivery of clinical studies in CVRM, and act as main liaison between study teams and the Clinical Program Team.

You will develop study level documents, oversee external partners, ensure systems are current, and drive performance against plans and KPIs, including budget re-forecasts throughout the study lifecycle.