Director, Clinical Trial Liaison - West
$253,000 - $329,000 per year
Apply now (opens in a new tab)Director, Clinical Trial Liaison - West
L7
$253,000 - $329,000 per year
Industries
Research and Development in the Physical, Engineering, and Life SciencesResearch and Development in BiotechnologyOffices of Physicians- 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.
- Minimum Bachelor's degree, master's preferred or terminal degree (MD, PhD or PharmD)10+ years relevant industry and/or CRO experience required
- Extensive experience in site facing clinical trial operations required
- Cardiovascular clinical trial experience and expertise in cardiovascular disease (e.g., heart failure, cardiomyopathies, hypertension, cardiometabolic disease, etc.) preferred
- Extensive medical and scientific knowledge and clinical development understanding
- Excellent communicator of technical and scientific information
- Excellent interpersonal skills and demonstrated collaborative as well as independent working style
- Ability to build relations with the external medical community
- Proactive and self-motivated, ability to align activities with the clinical development plans (CDPs)
- Strong organizational skills with effective use of time and prioritization
- Cross cultural awareness
- Fluency in English and in local language in country of residence required
- A working knowledge of ICH/GCPComputer skills including Excel, Word, and PowerPoint
Level
ManagerL7
Salary
$253,000 - $329,000 per year
Location
Denver, CO
Occupation
Clinical Research Coordinators
Industry
Research and Development in the Physical, Engineering, and Life Sciences
Posted
yesterday
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