Senior Clinical Trial Manager

This is a fully remote position, open to applicants in Spain.

📋 Description

• Implement one or more components of clinical studies while adhering to ICH/GCP, global regulations, and AbbVie policies and procedures.

• Assist the Study Project Manager in guiding the cross-functional study team.

• Organize Clinical Study Team meeting agendas and document minutes.

• Provide consistent updates on study status to the cross-functional team and stakeholders.

• Maintain the CTMS (Clinical Trial Management System) accurately.

• Aid in the development of the clinical study blueprint/protocol along with related systems and documentation, which includes informed consent forms, eCRFs, IRT, and CSR.

• Assist with vendor selection, scope development, management, and oversight.

• Create training materials related to the study for study teams, study sites, and vendors.

• Actively identify, address, and/or escalate study-related issues.

• Engage in initiatives aimed at process improvements.

⛳️ Requirements

• A Bachelor’s Degree or an equivalent degree from outside the U.S., typically in a nursing or scientific field, is required.

• A Registered Nurse licensure with an Associate’s Degree in Nursing accompanied by relevant experience is also acceptable.

• A minimum of four years of experience in Pharma-related or clinical research fields.

• Proven high level of core and technical competencies.

• Strong communication skills.

• Familiarity with standard business practices, Standard Operating Procedures, ICH guidelines, Global Regulations, Ethics, and Compliance.

• Preferred experience from study initiation through to study completion.

• At least three years of experience in clinical trial management roles.

• Proficient in English (C1 level).

• Must reside in Madrid.

🏝️ Benefits

• Flexible remote work options.

• Commitment to equal opportunity employment.

• Employer support for reasonable accommodations.