Senior Start Up Manager

Study Start Up Manager 

📍 Barcelona (3 days on-site / 2 days remote)

Make an impact where it matters most.

At Morgan Philips, we are looking for a Study Start-Up Manager to help accelerate patient access to cutting-edge oncology treatments for a leading global pharmaceutical company.

In this role, you will support the timely and compliant activation of clinical trial sites, contributing to the delivery of studies across a diverse portfolio, including oncology. You will work at the intersection of regulatory, operational, and cross-functional teams to ensure that study start-up activities are executed efficiently and in line with required standards.

What you’ll be doing

You will play a critical role within a high-performing local study delivery team, partnering cross-functionally with stakeholders to ensure timely and compliant study start-up.

• Support and coordinate clinical study start-up activities through to site activation.
• Ensure all documentation is complete and compliant with UCH-GCP and internal procedures.  
• Collaborate with cross-functional teams including Contracts, Feasibility, and Study Support Services.
• Track and share site activation progress and metrics with relevant stakeholders.
• Identify potential delays or risks in start-up activities and escalate as needed.
• Review site-level Informed Consent Forms (ICFs).
• Maintain and update systems such as Veeva Clinical Vault and other tracking tools.
• Ensure Trial Master File completeness and readiness for audits and inspections.
• Support preparation and documentation for regulatory submissions and inspections.
• Contribute to the creation and management of clinical-regulatory documents in internal systems.

What you bring

• Bachelor’s degree in a relevant field.
• +4 years of experience in study management or study start-up lead within a pharmaceutical environment.
• Knowledge of clinical trial regulations and study management practices.
• Fluency in English and Spanish.

What sets you apart

• Advanced degree within the field.
• ​Professional certification.
• Understanding of multiple aspects within Study Management.

Why this opportunity?

• Join a global leader in oncology innovation with a robust and diverse pipeline.
• Be part of a company committed to scientific excellence and patient impact.
• Work in an international, collaborative environment where your voice matters.

If you’re ready to take ownership of local study start-up activities and contribute to accelerating breakthrough treatments, this is your opportunity to make a real difference.

👉 Apply now!