Purpose : Serve as a key member of a strategic start-up function in support of clinical program objectives. Apply project management methodology and tools to facilitate delivery of milestones & activities during study-start up.
Support continuous improvement initiatives focused on driving efficient and effective processes to meet trial timelines and organizational objectives.Responsibilities :
Execute such start up activities as (but not limited to) country and site feasibility, site selection, site activation, informed consent, development, etc.
by interfacing with country personnel & affiliates, document management, and sites as needed
Serve to execute regulatory and IRB / EC submissions; document collection; site contracting; etc via collaborative partnerships with Doc Management , site management and monitoring, Regulatory, legal, and contracting
Collect and gather benchmarking data across all disease areas / indications in support of business planning; business development;
and program planning activities
Support implementation of study and site start-up initiatives to meet regulatory requirements outside of US (OUS), and maintaining alignment with clinical program timelines to achieve business objectives
Must have a Bachelor's Degree in a scientific or medical field, or equivalent with relevant experience
Must have a minimum of 3 years of hands on experience in clinical study management, ICF / GCP clinical research regulations and local rial start-up and management.
Must be able to understand the local environment from an operations as well as from a regulatory / GCP perspective.
Must have experience building effective working relationships across functions and geographic locations
Job Level Code
Equal Employment Opportunity
At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients.
As an equal opportunity employer we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic.