Clinical Trial Liaison

Role Summary

This role is responsible for maximizing site performance and site engagement in clinical studies. Leveraging strong clinical operational and therapeutic expertise to support execution of clinical studies. Engages with clinical sites to develop, build, and maintain strong relationships with investigators/staff to support clinical development programs. Provide operational support to deliver the study within planned timelines and quality standards. Evaluate, screen and develop high-quality investigative sites to support clinical development programs.

Responsibilities

• Develop, communicate, and execute Site Engagement Strategy/Plan working closely with the Clinical Team and key internal stakeholders throughout the life cycle of clinical trials
• Support the clinical team in coordinating and executing site engagement activities by understanding the competitive landscape, capturing trial roadblocks, and using motivational tactics to ensure the timely delivery of trials
• Engage, evaluate, and develop a network of high-performing sites through coordinated, consistent interactions using multiple communication channels to create awareness of its activities thereby increasing their desire to partner with ProKidney
• Develop & maintain relationships with site engagement organizations; assist identification of high-performing sites and key opinion leaders that can contribute to forums, boards and/or discussions.
• Interact/train new investigators to work on clinical trials ensuring the clinical and scientific understanding of the trial
• Support site with enrollment, including the development of patient material, advertisement materials, new requests for concierge services for participants (including travel/accommodation/appreciation items)
• Serve as primary contact for biopsy and/or procedure injections scheduling, logistics and
• Support site with screen failures during the enrollment phase, including pre-screening activities to improve patient selection and trial readiness

Monitoring Deliverables

• Responsible for attending Site Initiation Visits and managing the sites‚Äô performance regarding protocol and procedure knowledge and support
• Acts as the primary contact for the site regarding the general organization of the study, timelines, status, educational needs, and process flows.
• Responsible for the early engagement with Key Opinion Leaders (KOLs)/sites/patients organizations and key contact points for these throughout the study.
• Interact/train new investigators to work on clinical
• Attend key therapeutic training/meetings and/or industry
• Close collaboration and partnership with CRO to inform of all aspects of the clinical trial status at the site.
• Ensure appropriate engagement and communication with internal stakeholders regarding site visits and related activities.
• Support the development of presentations at Investigator Meetings or other trial-related
• Contributes to updates of clinical program information, e.g., annual safety updates, Investigator‚Äôs Brochure, and on query resolution, as needed, etc.
• In collaboration with CPM/study team, ensure that the study is audit/inspection ready and any resulting findings from audits/inspections are addressed appropriately and in a timely manner.

Qualifications

• Bachelor's Degree Preferably in life/physical sciences, RN or clinical degree highly preferred.
• Experience working in renal therapeutic area required
• Strong scientific background with at least 5 years of experience in Clinical Operations, Clinical Development, or as a Clinical Trial Liaison or Medical Science Liaison.
• Strong understanding of start-up activities, clinical trial planning, (site) management, and metrics.
• Strong communication and leadership
• Travel required to Boston and Raleigh HQs for team meetings as needed