Global Study Associate Onco (TEMP Big Pharma)

Randstad España; Barcelona; Híbrido; EUR 30.000 - 40.000; Jornada completa

Descripción de la vacante

A global biopharmaceutical firm is seeking a Global Study Associate for its Barcelona hub. This role involves managing study documents, supporting compliance, and coordinating study operations. Candidates should have a Bachelor’s degree in a relevant field and 1-2 years of experience in clinical studies. This temporary position offers an attractive compensation package and smartworking options.

Servicios

Attractive compensation package

Smartworking policy

Temporary contract

Formación

• 1-2 years’ experience in administrative support of clinical studies.
• Excellent communication skills and ability to lead tasks.
• Demonstrated knowledge of ICH-GCP principles.

Responsabilidades

• Collect, review, and track study documents.
• Support production and compliance of study documents.
• Manage and coordinate study materials and invoices.

Conocimientos

Administrative support

Knowledge of ICH-GCP principles

Team orientation

Communication skills

Proactive approach

Task management

Educación

Bachelor’s degree in medical or biological science

Descripción del empleo

AstraZeneca is looking for a Global Study Associate or CTA for its global hub in Barcelona for a temporary contract.

Typical Accountabilities

• Collect, review and track relevant study documents.
• Support production of study documents, ensuring template and version compliance and that relevant documents are ready for publishing in the regulatory document management system.
• Set-up, populate and accurately maintain information in tracking systems and communication tools. Support other study team members in the use of these systems.
• Manage and contribute to the coordination and tracking of study materials and equipment.
• Assist in the tracking and reconciliation of invoices.
• Support study team and provide study metrics / reports during the study, audits and regulatory inspections.
• Lead the practical arrangements and contribute to the preparation of internal and external meetings e.g. study team meetings, monitor meetings, investigator meetings and advisory boards.
• Liaise with internal and external participants and / or vendors. Track approvals and completion of required documents.
• Prepare and distribute study-related correspondence. Contribute to and distribute material for meetings, newsletters and websites.

Requirements

University degree / Bachelor’s degree, preferably in medical or biological science, or discipline associated with Clinical Research.

Minimum of 1-2 years’ experience of administrative / operational support of clinical studies

Excellent knowledge of ICH-GCP principles

Team orientated

Ability to lead, coordinate and prioritise multiple tasks and deliverables

Proactive approach

High degree of flexibility

Demonstrated verbal and written communication skills

Offered

• Temporary contract of at less than seven months
• Onboarding in February
• Attractive compensation package
• Smartworking policy

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