Study Project Manager II Oncology

Allergan; Madrid; A distancia; EUR 30.000 - 50.000; Jornada completa

Descripción de la vacante

A global pharmaceutical company is seeking a Study Project Manager II Oncology to drive the execution of clinical research studies. The role requires at least 8 years of experience in pharma or clinical research, specifically in oncology studies. Responsibilities include defining operational strategies, leading clinical studies, and managing cross-functional teams. This position supports home-based work and offers competitive pay.

Formación

• 8 years of pharma-related or clinical research experience required.
• Experience in Oncology studies within the last 5 years.
• Expertise in managing all phases of clinical studies.

Responsabilidades

• Define operational strategies linking to asset goals.
• Execute clinical studies following quality standards.
• Lead cross-functional teams and influence stakeholders.

Conocimientos

Clinical study operations management

Project Management in interventional trials

Strategic asset level thinking

Stakeholder management

Innovation

Educación

Bachelor’s Degree or equivalent

Descripción del empleo

Overview

The Study Project Manager II Oncology drives the connection between the asset and operational delivery and execution of one or more clinical research studies. Leading the delivery of clinical operational strategies to ensure studies are executed with quality and efficiency, on-time, within budget, and meet company objectives. The Study Project Manager II achieves these objectives by bringing scientific acumen, strategic asset level thinking, innovation, expertise in clinical study operations management and stakeholder management to address risks and challenges.

Responsibilities

• Defines and drives the study level operational strategies and deliverables – linking these to asset level goals
• Brings strategic, asset level thinking and innovative problem solving to study planning and execution
• Responsible for executing clinical studies in compliance with quality standards (ICH/GCP, Global Regulations, and AbbVie policies and procedures).
• Effectively present and contribute to discussions on study operations at asset level strategic meetings
• Leads clinical operations planning through to execution via cross functional matrix environment and influences cross functional stakeholders to drive milestone achievement
• Demonstrates the skills, experience and critical thinking to lead cross functional teams with minimal supervision.
• Expertise in end-to-end clinical study operations management (all phases, set up to close out)
• Coaches and mentors team members, delegates and empowers to the right level, actively contributes to Development Operations community
• Demonstrates leadership with high level cross functional stakeholder management and influencing skills
• Lead operational efficiencies and foster a culture of innovation

Qualifications

• Bachelor’s Degree or equivalent degree is required
• 8 years of demonstrated pharma-related and/or clinical research related experience or equivalent required.
• Exposure in study initiation through study completion in Phase 1-4 and/or Medical Device Trial Experience
• No direct reports, but matrix management.
• Required experience in Project Management interventional trials
• Experience in Oncology studies in the last 5 years of experience.
• Homebased.

Additional Information

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

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