Note: The job is a remote job and is open to candidates in USA. Worldwide Clinical Trials is a contract research organization conducting clinical research. The Clinical Trials Associate provides administrative and project-tracking support to clinical project teams, helping ensure assigned project tasks are completed accurately and on time.
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
Skills
- Excellent written and verbal English as well as fluency of the language of the country of location
- 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
- 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
Company Overview
Company H1B Sponsorship