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;
Remote position based in Madrid.
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