Clinical Project Manager, IQVIA Biotech Immuno-Oncology and Cell and Gene Therapy (EMEA)

QPL IQVIA RDS Poland Sp. z o.o.; Madrid; Presencial; EUR 50.000 - 70.000; Jornada completa

Descripción de la vacante

A leading global healthcare solutions company is seeking a Clinical Project Manager for their Immuno-Oncology and Cell and Gene Therapy Unit in Madrid, Spain. This role involves managing cross-functional teams and ensuring project milestones and quality. The ideal candidate will have a Bachelor's degree in life sciences, 2-4 years of project management experience in the drug development industry, and knowledge in Cell and Gene Therapies. Responsibilities include leading project delivery and acting as the main contact for customers.

Formación

• Minimum 2-4 years prior project management experience in the drug development industry.
• Must have previous CRO experience.
• In-depth knowledge of First in Human and Paediatric Oncology.

Responsabilidades

• Lead global cross-functional project team delivery.
• Serve as the primary contact with the customer for progress.
• Manage study team assignments and resource requirements.

Conocimientos

Global project management experience

Knowledge in Cell and Gene Therapies

Experience in clinical operations

Educación

Bachelor's degree in life sciences or related field

Descripción del empleo

Overview

Clinical Project Manager — Immuno-Oncology and Cell and Gene Therapy

IQVIA Biotech

IQVIA’s Biotech Immuno-Oncology and Gene Therapy Unit is a global team of professionals dedicated to assisting our clients in driving healthcare forward and enabling medical breakthroughs that advance healthcare and patient treatment options around the world.

Role

As a Clinical Project Manager you will manage cross functional teams and liaise directly between IQVIA Biotech functions and the customer, acting as that accountable point for delivery and quality whilst maintaining financial control. You will be supported by domain experts in every function, enabled by best-in-class technology and data analytics.

Key collaborators

This role collaborates with the Clinical Lead for site management, the Project Vendor Manager, the Project Management Analyst for project coordination, tracking and financial analysis, and the Site Activation Manager as an expert in start-up.

This is an important and high-profile role within our Research & Development Operation and IQVIA Biotech’s size and global footprint will present you with the breadth of opportunities necessary to develop your career.

Responsibilities

• Leading global cross-functional project team delivery, accountable for achievement of milestones and quality of contracted scope
• Serving as the primary contact with the customer for progress and governance
• Developing study management plans and ensuring consistent use of study tools, training materials and compliance with standard processes, policies and procedures
• Anticipating risk and implementing mitigation strategies
• Managing study team assignments, accountability and resource requirements
• Ensuring the study budget is managed proactively including scope changes and financial systems are accurate

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

• Bachelor's degree in life sciences or related field
• Global project management experience within the drug development industry, with previous CRO experience is a must
• Minimum 2-4 years prior project management experience and experience in clinical operations; or equivalent combination of education, training and experience
• In depth therapeutic knowledge in Cell and Gene Therapies, First in Human and Paediatric Oncology