AbbVie is a global, research-driven biopharmaceutical company focused on developing innovative therapies for some of the world's most complex and critical conditions. Spun off from Abbott Laboratories in 2013, the company operates in key therapeutic areas including immunology, oncology, neuroscience, and eye care. With a workforce of approximately 50,000 employees worldwide, AbbVie is a major player in the pharmaceutical industry, consistently ranking among the top companies for research and development investment. In Spain, AbbVie maintains a robust presence with its commercial headquarters located in Madrid and a significant manufacturing facility in Tres Cantos. The company is recognized for its high-performance culture and commitment to diversity, making it an attractive destination for international professionals in medical affairs, clinical research, and specialized marketing. While many field-based roles require local language proficiency, the company's global nature provides opportunities for cross-border collaboration and career progression within the European market.

AbbVie was formed in 2013 following the separation from Abbott Laboratories. Since its inception, it has grown into a leading biopharmaceutical entity through significant R&D and strategic acquisitions, such as Allergan in 2020.

Senior Clinical Trial Manager

AbbVie

Requirements

Qualifications

•Bachelor’s Degree or OUS equivalent degree required, typically in nursing or scientific field; Registered Nurse licensure with Associate’s Degree in Nursing with relevant experience is also acceptable.
•Must have at least four years of Pharma-related/clinical research related experience and demonstrated a high level of core and technical competencies.
•Possesses good communication skills.
•Competent in application of standard business procedures {Standard operating procedures, International Conference on Harmonization {ICH), Global Regulations, Ethics and Compliance).
•Preferred exposure to study initiation through study completion.

•Remote position based in Madrid..

Benefits

Additional Information

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

Original Advert

Company Description

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

Job Description

•Responsible for executing one or more elements of clinical studies in compliance with quality standards (ICH/GCP, Global Regulations, and AbbVie policies and procedures).
• Supports the Study Project Manager in leading the cross functional study team: o -Supports the preparation of Clinical Study Team meetings (Agenda/Minutes) o -Responsible for regular updates to the cross-functional team and stakeholders on study status; ensure our CTMS is up to date
•Supports the development of the clinical study blueprint/protocol and associated systems and documents (Informed consent forms, eCRFs, IRT, CSR)
•Supports the vendor selection, scope development, management and oversight of external vendors in compliance with AbbVie's processes and procedures and the applicable regulations.
•Responsible for generating the study related training for the study team, study sites, and vendors for assigned studies
•Proactively identify and resolve and/or escalate study related issues
•Participates in process improvement initiatives