Covance Project Support Coord I in Leeds, United Kingdom
As Project Support Coordinator, you will have primary responsibility for the coordination and completion of all administrative functions in support of the project manager for overall multi-site clinical studies. This is an ideal opportunity for recent graduate with some relevent work experience looking to establish their career within one of the worlds leading CRO's.
Provides administrative support for effective Clinical Trial Core Team Operations
Consistently comply with GCP
Learns and applies drug development process knowledge including GCP
Original document management
CTMS/eTMF set up per BP&S standards
Develop Inv Training
Granting EDC access, and access to other study required systems
CTMS Data Monitoring
Payments per Global Finance standards
Coordinates Study/Sponsor Specific Training in iLearn
Performs other duties as assigned by management to support study teams needing collaborative support
Education / Qualifications
University/college degree, or certification in a related allied health profession (i.e. nursing, medical or laboratory technology), in lieu of college degree candidate may have relevant industry experience.
Knowledge of the clinical trial process with early clinical pharmacology experience preferred
Computer competency with various programs (e.g., Microsoft Word, Excel, Project, Access and Power Point)
Some previous relevant industry experience.
Additional experience may be substituted for education requirements
Job Number 2018-20595
Job Category Clinical Operations
Position Type Full-Time
Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran/Sexual Orientation/Gender Identity). Your confidentiality and privacy are important to us.