We are 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.
Requirements
- 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, ensuring sites understand study objectives, rationale, investigational product profile, and any updates or amendments.
- Collaborate with Clinical Operations and Clinical Development
- Participate in clinical study team meetings and quality meetings where necessary providing input to study teams on operational issues based on site visits and contacts
- Attend and present at SIVs, investigator meetings, monitor workshops/training
- Participate in site visits with investigator site staff and/or CRO representatives, or independently, in support of clinical trial execution and report back to study teams e.g. feasibility, startup activities, enrolment or escalated study/site issues
- 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
- Provides 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 including but not limited to required training, field activity documentation, expense reporting, and other assigned tasks
- 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.
- Ensure all interactions comply with regulatory, ethical, and company standards.
Benefits
- Generous Paid Time Off
- 401k Matching
- Retirement Plan
- Health insurance
- Dental insurance
- Vision insurance
- Life insurance
- Disability insurance
