Clinical Trial Manager

About the role

Bristol Myers Squibb is looking for a Clinical Trial Manager in Madrid. The manager is accountable for end-to-end study operational oversight and delivery at country level, ensuring adherence to timelines, budget and quality standards, and acts as the main point of contact for internal and external stakeholders.

Key responsibilities

• Coordinate the country with global study team members and local cross-functional teams, and implement the local feasibility process and study targets
• Plan and execute start-up timelines, patient recruitment strategy and enrolment targets, and lead risk management and escalation
• Assess and set up vendors, prepare investigator meetings and verify that CTMS data, eDC and eTMF access are available
• Validate study materials (protocol, informed consent forms, patient materials) and support site initiation visits and site closure
• Ensure inspection readiness, support health authority and ethics committee submissions, and drive CAPA implementation
• Support site relationships, site monitoring reports, database locks and query follow-up, and coordinate study team meetings

Required profile

• Bachelor's or master's degree in life sciences or equivalent
• Minimum 4 years of industry experience; senior Clinical Trial Managers need at least 6 years
• Experience leading or taking part in cross-functional teams, task forces or local and global initiatives
• Ability to mentor peers and act as a subject matter expert
• Good verbal and written communication in English and the local language

Required skills

• Deep understanding of GCP, ICH guidelines and local clinical research regulations
• Independent use of Microsoft Suite, CTMS, eDC and eTMF