Senior Clinical Trial Manager

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

📋 Description

• Implement one or more components of clinical trials in accordance with ICH/GCP, Global Regulations, and AbbVie policies and procedures.

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

• Aid in the preparation of Clinical Study Team meetings, including the organization of agendas and minutes.

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

• Ensure the CTMS is maintained and current.

• Contribute to the development of the clinical study blueprint/protocol along with related systems and documentation, such as informed consent forms, eCRFs, IRT, and CSR.

• Assist with vendor selection, scope development, management, and supervision while adhering to relevant processes and regulations.

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

• Proactively identify, resolve, and/or escalate issues related to the study.

• Engage in process improvement initiatives.

⛳️ Requirements

• Bachelor’s Degree or equivalent overseas qualification, typically in nursing or a scientific discipline.

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

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

• Proven high level of core and technical competencies.

• Strong communication skills.

• Proficiency in standard business operations, including Standard Operating Procedures, ICH, Global Regulations, Ethics, and Compliance.

• Preferred experience in study initiation through to study completion.

• At least 3 years in roles related to clinical trial management.

• Fluent in English (C1).

🏝️ Benefits

• Remote position / employees can work from home.

• Equal opportunity employer.

• Commitment to operating with integrity, fostering innovation, transforming lives, and serving the community.