Senior Clinical Trial Manager (Clinical Research)

Location: Remote position based in Madrid, Spain

Company

Develops innovative medicines and solutions for serious health issues across immunology, oncology, neuroscience, and aesthetics.

What you will do

• Execute one or more elements of clinical studies in compliance with ICH/GCP, global regulations, and internal procedures.
• Support the Study Project Manager and cross-functional study team through meeting preparation, status updates, stakeholder communication, and CTMS maintenance.
• Support development of clinical study protocols, blueprints, informed consent forms, eCRFs, IRT, CSRs, and related systems.
• Support vendor selection, scope development, management, and oversight.
• Generate study-related training for study teams, sites, and vendors.
• Identify, resolve, and escalate study issues while contributing to process improvement initiatives.

Requirements

• Bachelor's degree or equivalent, typically in nursing or a scientific field; an Associate Degree in Nursing with relevant experience and Registered Nurse licensure is also acceptable.
• At least four years of pharmaceutical or clinical research experience.
• At least three years of experience in clinical trial management positions.
• Strong communication skills and competence with standard business procedures, ICH, global regulations, ethics, and compliance.
• Fluent English at C1 level required.

Nice to have

• Exposure to clinical studies from initiation through completion.

Culture & Benefits

• Remote work arrangement based in Madrid.
• Commitment to integrity, innovation, transforming lives, and serving the community.
• Equal opportunity employment.