Kardigan is seeking a Director, Clinical Trial Liaison to develop relationships with clinical trial investigators and research site staff to facilitate recruitment of subjects in Kardigan clinical trials. The successful candidate will support Global Development clinical study execution as the local field-based representative for Kardigan in the Northern Midwest region, covering Illinois, Indiana, Michigan, Minnesota, Missouri, Iowa, and North Dakota.
Requirements
- Develop relationships with clinical trial investigators and research site staff
- Support Global Development clinical study execution as the local field-based representative for Kardigan
- Provide country/regional operational insight into site feasibility and selection and overall patient recruitment strategy
- Identify and cultivate high-quality cardiovascular investigators
- Communicate scientific and clinical information clearly and accurately
- Collaborate with Clinical Operations and Clinical Development
- Participate in clinical study team meetings and quality meetings
- Attend and present at SIVs, investigator meetings, monitor workshops/training
- Support enrollment and retention efforts through tailored discussion, data-driven insights, and strong relationship-building
- Responsible for review, documentation and follow up of investigator site issues including tracking metrics
- Provide sponsor regional operational support and acts as point of escalation for investigator sites as appropriate
- Identify and escalate site needs, barriers, or operational challenges to the Clinical Operations and Medical teams
- Participate in Regulatory GCP inspections and/or audits at investigator sites as sponsor representative
- Complete all administrative responsibilities consistent with SOPs and departmental guidelines
- Understand the scientific basis of assigned clinical trials
- Support creation of educational materials to effectively communicate the science behind the clinical trial
- Be able to communicate the scientific basis of the trials to other team members, investigators and site staff
- Identify effective prescreening strategies for each trial and recommend improvements
- Provide detailed reports of interactions with investigators and site staff
- Partner with Medical Affairs, Clinical Operations, and other cross-functional stakeholders to ensure consistent messaging and aligned site support
Benefits
- Generous Paid Time Off
- 401k Matching
- Retirement Plan
- Visa Sponsorship
