What are the responsibilities and job description for the Project Coordinator - Clinical Trials position at ICON Strategic Solutions?
**About This Role**
We are seeking an experienced Technical ePRO Project Manager to join our team. The successful candidate will be responsible for managing the translation process and timelines with vendors, kickoff ePRO development, draft/finalize user requirement specifications, execute UAT scripts / change requests, establish Project Plan via Microsoft Project, manage ePRO project schedule, coordinate resolution & risk mitigation of all ePRO / eCOA-related issues and end-of-study vendor deliverables, write / update standard operating procedures, develop a library of ePRO data capture and reporting standards, as needed.
**Responsibilities Include:**
- Manage translation process and timelines with vendors
- Kickoff ePRO development
- Draft/finalize user requirement specifications
- Execute UAT scripts / change requests
- Establish Project Plan via Microsoft Project
- Manage ePRO project schedule
- Coordinate resolution & risk mitigation of all ePRO / eCOA-related issues and end-of-study vendor deliverables
- Write / update standard operating procedures, develop a library of ePRO data capture and reporting standards, as needed
**Requirements:**
To be successful in this role, you will need:
- Experience in managing technical projects, preferably in the pharmaceutical or biotechnology industry
- Strong communication and interpersonal skills
- Ability to work in a fast-paced environment and prioritize multiple tasks
- Proficiency in Microsoft Project and other project management tools
**What We Offer:**
We offer a competitive salary and benefits package, including health insurance, retirement plan, and paid time off.
