Senior Clinical Trial Manager

Description

**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 **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. * At least 3 years in clinical trial management positions. * Fluent in English (C1\) * Remote position based in Madrid. **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