Description:
- The efficient day-to-day management of LVG trials consistent with Good Clinical Practice and Data Protection requirements
- Ensure procedures adhere to regulatory and ethical requirements and the trial protocol
- Develop monitoring systems and conduct quality control processes to ensure trials are managed within the time frame that adhere to regulatory, ethical requirements consistent with the trial protocol
- Communicate with stakeholders to ensure protocol requirements are met
- Promote recruitment of research participants by actively attending public events and presenting the trial
- Provide training in trial management processes to the LVG team
- Support investigators with submission of qrants.
The ideal candidate will have a degree in a related scientific subject, coupled with experience in the management and co-ordination of clinical trials. A sound appreciation of GCP and regulatory/ethical requirements is essential, as is a proven track record of working in a clinical or medical research environment. We need someone with the ability to thrive in a team environment as well as being able to deliver in a meticulous and accurate manner as an individual. Ideally you will be able to demonstrate:
- A degree or equivalent in a related scientific subject
- Excellent understanding of GCP and regulatory /ethical requirements
- Experience of database cleaning and management
- Trial design, supporting grant applications and/or statistics (desirable)
- Demonstrate excellent teaching skills/clinical teaching skills with the ability to teach post-graduate students
- Excellent time management and organisational skills
- Strong interpersonal skills with the ability to create and maintain strong inter- disciplinary relationships
- Ability to work under pressure to meet tight timelines
- Ability to show initiative, provide solutions to problems and have the confidence in taking decisions