Project Coordinator
On-siteBethlehem, Pennsylvania, United States or Rhymney, Wales, United Kingdom
Job Summary
Work closely with IRT Project Managers on assigned study support tasks to meet project deliverables and milestones within the various stages of the project life cycle. Serve as an additional point of contact to sponsors, sponsor vendors, and sites. Resolve or escalate study support issues in accordance with processes, work instructions and standard operating procedures (SOP). Develop project specific import/export and report specifications. Assist with the set-up of client acceptance testing (CAT). Collect, document, and perform requested parameter and data changes in alignment with documented procedures. Create, revise, and maintain study specific documents such as user guides. Collaborate with internal teams and sponsors to create and maintain study specific training materials. Monitor study specific IRT issues and resolutions for trends. Provide urgent study specific support after normal business hours as needed.
Required Qualifications
- Associate's degree
- Previous exposure to clinical trials
- Basic understanding of medical and/or clinical trial terminology
Desired Qualifications
- Previous experience with clinical trials in a client-facing role
- Experience working with computer software including Word, Excel and Access
- Ability to work independently and to adjust to changing priorities
- Excellent attention to detail and orientation toward project work
- Strong verbal and written communication skills
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