Covance Project Support Coord I in Leeds, United Kingdom

Job Overview

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.

Main Responsibilities:

  • Provides administrative support for effective Clinical Trial Core Team Operations

  • Consistently comply with GCP

  • Learns and applies drug development process knowledge including GCP

  • Study Plans

  • 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

  • Trackers

  • Coordinates Study/Sponsor Specific Training in iLearn

  • Performs other duties as assigned by management to support study teams needing collaborative support

Education / Qualifications

Recommended:

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)

Experience

Minimum Required:

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.