Global Study Associate Manager

AstraZeneca; Barcelona; Presencial; EUR 30.000 - 50.000; Jornada completa

Descripción de la vacante

A leading pharmaceutical company based in Barcelona is seeking a Global Study Associate Manager. This role involves managing clinical study execution, collaborating with global teams, and overseeing compliance systems. Candidates should possess a Bachelor's degree in a relevant field, with over 3 years of experience in clinical research. The company promotes a culture of diversity and inclusion, offering tailored development programs to support employee growth. Apply now to make a meaningful impact in clinical studies!

Formación

• 3+ years of experience supporting global study teams in clinical research.
• Ability to drive discussions around project scope.
• Knowledge of Essential Documents, CFR, and/or ICH-GCP.

Responsabilidades

• Collaborate with global study teams to support clinical studies.
• Prepare study and vendor-related documents.
• Identify risks and contribute to mitigation plans.
• Support project and budget management.

Conocimientos

Fluency in English

Excellent organizational communication

Proficiency with Microsoft Office

Strong relationship building skills

Highly proactive

Educación

Bachelor’s degree in clinical practice/health care or life sciences

Herramientas

Microsoft Excel

Microsoft PowerPoint

SharePoint Online

eTMF

Veeva Systems

Descripción del empleo

Introduction to role:

This role is based in Barcelona, with an on-site commitment of three days a week. Fluency in English is required.

Are you ready to make a difference in the world of clinical studies? As a Global Study Associate Manager (GSAM) at AstraZeneca, you'll be an integral part of our Development Operations team, supporting the delivery of clinical studies from inception to completion. You'll work alongside internal and external partners to ensure the successful execution of clinical studies across various therapeutic areas and phases. Your role will involve assisting global study teams, leading administrative activities, overseeing compliance tracking systems, and supporting vendor oversight. This is your chance to contribute to life-changing research!

Accountabilities:

• Collaborate with global study teams and key vendors to support clinical study execution, ensuring adherence to timelines and quality standards.
• Lead the preparation of study documents and vendor-related documents, such as the Vendor Oversight Plan.
• Maintain and facilitate interactions with cross-functional team members, including Data Management, Procurement, Regulatory, Patient Safety, and Quality Assurance.
• Execute delegated aspects of the clinical study in alignment with objectives set by GPD, GSAD, or GSM.
• Contribute to the planning and execution of internal and external meetings.
• Identify risks and issues, contributing to the development of mitigation and action plans.
• Support project and budget management in collaboration with the GSM.
• Participate in departmental initiatives and serve as a mentor for team members.
• Provide support for other study and functional activities as assigned.

Essential Skills/Experience:

• Bachelor’s degree or equivalent in clinical practice/health care, life sciences, or drug development, or commensurate work experience.
• Proficiency with technological systems (Microsoft Office such as: Excel, PowerPoint, and SharePoint Online, eTMF and Veeva Systems).
• Excellent organizational communication and time management skills.
• Highly proactive and willing to take initiative.
• Strong relationship building skills.
• The duties of this role are generally conducted in an office environment. As is typical of an office-based role, employees must be able, with or without an accommodation to: use a computer; engage in communications via phone, video, and electronic messaging; engage in problem solving and non-linear thought, analysis, and dialogue; collaborate with others; maintain general availability during standard business hours.

Desirable Skills/Experience:

• Over 3 years supporting global study teams in a clinical research environment.
• Ability to drive discussions around the scope of work and oversee vendor-related activities.
• Excellent knowledge of Essential Documents, CFR, and/or ICH-GCP.
• Demonstrated ability to collaborate as well as work independently.
• Project management skills and basic PM methodology.

When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.

At AstraZeneca, we are driven by a passion for innovation and a commitment to making a meaningful impact on patients' lives. Our culture values diversity and inclusion, fostering an environment where new ideas can thrive. We are dedicated to supporting our employees' growth through tailored development programs that align with our mission. By joining us, you'll be part of a team that is empowered to drive change with integrity and make a difference where it truly counts.

Ready to embark on this exciting journey with us? Apply now to become a part of our team!

Date Posted

03-dic-2025

Closing Date

16-dic-2025

Alexion is proud to be an Equal Employment Opportunity and Aff... The Company will not make decisions about employment, training, compensation, promotion, and other terms and conditions of employment based on race, color, religion, creed, sex, sexual orientation, age, ancestry, national origin, ethnicity, citizenship status, marital status, pregnancy, parental status, military status, protected veteran status, disability, medical condition, gender identity or expression, genetic information, mental illness or other characteristics protected by law. Alexion provides reasonable accommodations to meet the needs of candidates and employees. To begin an interactive dialogue with Alexion regarding an accommodation, please contact [e-mail]. Alexion participates in E-Verify.