Global Study Director – CVRM Clinical Operations

AstraZeneca GmbH

Mölndals kommun

On-site

SEK 1,000,000 - 1,500,000

Full time

14 days+

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Job summary

AstraZeneca is seeking a Global Study Associate Director in Gothenburg, Sweden, to lead cross-functional teams in CVRM clinical studies, directing study timelines, budgets, and quality. You will develop essential study documents and oversee external providers, ensuring systems and data stay current throughout the study lifecycle.

Ideal candidates bring extensive study management experience, strong ICH-GCP knowledge, and proven leadership in global clinical study settings.

Qualifications

University degree in medical or biological sciences.
Clinical research experience in pharma, including project management.
Extensive study management experience.
Strong knowledge of ICH-GCP and regulatory requirements.
Proven leadership and cross-functional team experience.

Responsibilities

Lead and guide a cross-functional study team to ensure timely, within-budget delivery.
Develop essential study-level documents and oversee external service providers.
Ensure study systems and data are current and accurate at the study level.
Monitor performance against plans, milestones and KPIs; manage study budget re-forecasting.
Collaborate with CPT and ensure compliance with quality standards across the study lifecycle.