About the Role
The Study Feasibility and Activation Manager is responsible for improving patient access to clinical trials. This role involves leading and conducting site feasibility, hospital approval processes, and set-up phases of clinical trials.
Key Responsibilities
* Guide sponsors through the start-up process to ensure a timely approach to study activation.
* Manage the feasibility assessment of the study and sites capacity, coordinate the legal agreement process and budget process, processing of the study application through the CRC and hospitals' approval process, liaise with the clinical team on their requirements to conduct the study and coordinate the activation of the study at the site.
* Coordinate and host feasibility meetings with sponsors and relevant clinical team members until study greenlight.
Requirements
* Degree in a relevant field, such as Nursing.
* Good Clinical Practice qualification required.
* Three years of experience as a clinical research nurse or other relevant degree with 3 years previous involvement in the conduct of clinical trials.
* Able to demonstrate knowledge of the potential steps in the feasibility process for research studies.
* Able to demonstrate experience in reviewing and understanding the requirements of a clinical trial protocol.
* Experience of supporting project plans and implementing them within agreed timelines.
RCSI Clinical Research Centre (RCSI-CRC) works to improve patient access to clinical trials. We seek an exceptional individual to take on the role of CRC Study Feasibility and Activation Manager to deliver the study feasibility and Start-up programme at RCSI-CRC.
The ideal candidate will have strong stakeholder management skills, a keen ability to positively influence and negotiate successful outcomes, and excellent communication skills with an ability to translate needs and guidance to both clinical and non-clinical stakeholders.