Clinical Trial Manager

AbbVie

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profile Job Location:

Madrid - Spain

profile Monthly Salary: Not Disclosed
Posted on: 30+ days ago
Vacancies: 1 Vacancy

Job Summary

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 AbbVies 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 :

Bachelors Degree or OUS equivalent degree required typically in nursing or scientific field; Registered Nurse licensure with Associates 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.
.


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

Work :

No


Employment Type :

Full-time

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 m...
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About Company

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AbbVie is a global biopharmaceutical company focused on creating medicines and solutions that put impact first — for patients, communities, and our world. We aim to address complex health issues and enhance people's lives through our core therapeutic areas: immunology, oncology, neuro ... View more

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