How can the NWORTH Trial Management team support your study?
The NWORTH Trial Management team work closely with Chief Investigators, Sponsors and site staff to manage and support trials from inception through to closure. Our Trial Managers coordinate and monitor the daily activities throughout the trial, including trial management & administration, data management, pharmacovigilance and quality control. They ensure the protocol is adhered to and your study runs on time, within budget and to target.
Our Trial Managers can support with:
- preparing funding applications, including costing and timelines
- drafting the protocol
- trial design and methodology development
- obtaining regulatory and ethical approvals
- selection and management of study sites, including set-up and training
- maintaining the Trial Master File (TMF) and trial documentation
- safety reporting and pharmacovigilance
- Daily monitoring and management throughout the study’s duration
- Closure and archiving
All NWORTH Trial Managers have detailed knowledge of Good Clinical Practice (GCP), the UK regulatory and ethical system and governance, and all clinical trial processes. Trial Managers work in accordance with NWORTH Standard Operating Procedures (SOPs), ensuring all trial activities adhere to relevant legislation.