Clinical Project Associate

The Clinical Project Associate is an integral member of the Operations department, providing support and troubleshooting on various aspects of projects for the clinical project teams.

Responsibilities:
- Attend local investigator and project specification design meetings.

- Participate in study design meetings along with the Clinical Project Manager, including teleconferences and in-person client meetings.

- Liaise with UK and inter-departmental colleagues on project-related issues.

- Provide backup to the Clinical Project Managers (CPMs) on project-related duties.

- Troubleshoot on live study issues for the Clinical Project Managers.

- Create end-user documentation, call flow charts and other study-related documents as necessary.

- Create unit testing for test plans and execute testing.

- Prepare and collate completed study validation packages for transfer to the UK for the Clinical Project Managers.

- Support the client testing process by being available to assist clients with any issues.

- Raise Project Amendment Forms (PAFs), test PAF changes and follow through to completion and go-live.

- Update Specifications and other study-related documentation as necessary.

- Communicate with clients as necessary on any aspect of the projects.

Qualifications:
This job requires a person to be highly customer focused with excellent computer skills, including proficiency with MS Office. This position requires organizational skills with a high attention for detail. The ability to work in a team environment, meet deadlines, and prioritize and balance work from multiple individuals is necessary. Excellent verbal and written communication skills are essential.

Bachelor's degree preferred with one to two years of experience working in a client-based environment within the CRO, research or biopharmaceutical industries.