£ 13.88 Per hour
Administrator
contract, Part time, Temporary
Job Description
- Work with the project plans, and help the CI to manage the timeline, project roles and responsibilities, risk assessments etc.
- Work with clinicians and researchers to prepare ethics and regulatory submissions, keeping a track of submissions, amendments & approvals.
- Work with clinicians and researchers to prepare and co-ordinate reports for ethics committees and funding body as required.
- Be responsible for the Trial Master File/s, all document control and office systems ensuring all essential trial documentation is complete, correct and readily available for use and review.
- Organize regular project meetings (both online and in person).
- Prepare agendas and take minutes for project meetings.
Required Knowledge, Skills, and Abilities
- Technical mind-set with the ability to quickly understand new software
- Excellent written and verbal communication skills with the ability to communicate effectively with a wide range of people
- Ability to support non-technical users
- Organized and methodical approach
Reference no: 98850