Clinical Trials Associate

Worldwide Clinical Trials•Carolina, NC

9h•$17 - $34

About The Position

The Clinical Trials Associate is responsible for providing administrative and project tracking support to the clinical project team, ensuring tasks for all assigned projects with Project Delivery services are performed timely and accurately.

Requirements

Degree level qualification or equivalent experience plus a minimum of one years’ experience in a related role
Skill sets and proven performance equivalent to the above
Excellent written and verbal English as well as fluency of the language of the country of location
Strong interpersonal skills
Ability to work independently and as a team member
Sense of urgency and ability to be adaptable in a fast-paced and rapidly changing environment
Ability to handle multiple tasks and exercise independent judgment
Strong attention to detail and focus on quality of work
Strong organizational and problem-solving skills
Excellent skills in MS Office applications including Outlook, Word, Excel and PowerPoint
Knowledge and understanding of ICH, GCP, and FDA or EU directive regulations (as applicable)

Responsibilities

Arrange and track system access for project team (Project Managers, Lead CRAs, CRAs, etc.)
Maintain and quality audit to assure the most recent revisions of documents are on project portals
Assist project team with preparation and shipment of clinical trial documentation, including Investigator Site File
Maintain version and quality control of project documentation and submit to trial master file
Assist with the tracking and maintenance of project related information, including site medical question and answer log
Generate and distribute minutes for a range of project related meetings, including Sponsor and Internal Management
Maintain current participating site and personnel information
Arrange and track the distribution of project specific training to the project team
Perform other duties as assigned