Global Feasibility Specialist

Global Feasibility Specialist (FSP)

Location: Remote – Spain

Advanced Clinical is looking for a Global Feasibility Specialist to join our growing Functional Service Provider (FSP) team, supporting a leading global biopharmaceutical company.

This is an excellent opportunity for an experienced feasibility professional who enjoys working independently, partnering with global study teams, and driving the feasibility strategy across international clinical trials.

Key Responsibilities

• Lead and coordinate global feasibility activities across Phase I–III clinical studies.
• Manage multiple feasibility projects simultaneously, supporting study start-up timelines.
• Partner closely with Clinical Trial Managers, Study Start-Up teams, Medical Science Liaisons, CROs and investigators.
• Design, launch and manage feasibility questionnaires and oversee response tracking and analysis.
• Analyse feasibility data to support country and site strategy recommendations.
• Utilise feasibility platforms and clinical systems to drive high-quality decision making.
• Identify opportunities to improve feasibility processes and operational efficiency.
• Collaborate with cross-functional stakeholders to ensure studies are delivered on schedule.

What We're Looking For

• Experience managing global feasibility activities within a sponsor or CRO environment.
• Experience supporting multiple Phase I–III studies simultaneously.
• Strong experience working directly with investigators, clinical sites and cross-functional study teams.
• Ability to work independently with minimal supervision.
• Experience analysing feasibility data and providing strategic recommendations.
• Strong project management, communication and stakeholder management skills.
• Good understanding of the clinical trial process and global clinical research operations.

Preferred Experience

• Experience with Veeva Feasibility would be highly advantageous.
• Experience using feasibility platforms such as goBalto or similar systems.
• Experience improving or optimising feasibility processes.
• Experience within rare disease studies would be beneficial.