Clinical Trial Liaison

This is a fully remote position, open to applicants in Kentucky, +2 more states.

📋 Description

• Oversee the comprehensive process of investigator engagement, from identification and qualification to enrollment, database lock, and study closeout.

• Act as a scientific ambassador for clinical trials, articulating the intent of protocols, their scientific rationale, and the criteria for patient eligibility.

• Build and maintain strategic relationships with investigators across various trials and therapeutic areas.

• Design customized recruitment strategies to enhance enrollment efforts.

• Identify avenues to connect with new patients, expedite enrollment, and amplify impact at key sites.

• Gather insights from sites to enhance feasibility, protocol design, and study execution.

• Spearhead site-level strategy and risk management for enrollment and data delivery.

• Employ performance metrics to foresee challenges and uphold progress towards clinical milestones.

• Ensure inspection readiness across all sites.

• Collaborate with various functions and vendors to eliminate operational obstacles.

• Influence strategic selection of countries/sites and protocol adaptation based on local treatment and standard-of-care knowledge.

• Oversee vendor monitoring with a focus on quality assurance.

• Where applicable, manage Post-Marketing Safety Studies from start to finish, ensuring compliance with local regulations.

• Develop a network of strategically aligned investigators who prioritize client trials.

• Collaborate with Medical, Clinical, Study Delivery, field teams, vendors, and investigators to synchronize priorities and enhance enrollment outcomes.

• Conduct data-driven site prospecting and prioritization.

• Lead scientific, therapeutic, and solution-oriented discussions with site personnel.

⛳️ Requirements

• Bachelor's degree or equivalent; a strong preference for backgrounds in scientific, clinical, or health-related fields.

• At least 5 years of experience in clinical research or the pharmaceutical industry, with direct interactions or collaborations with healthcare professionals and clinical sites.

• Willingness to travel 60-80% during peak periods (travel demands may vary).

• Experience in Neurodegenerative diseases/Alzheimer's is advantageous.

• Employment with ICON is contingent upon possessing the legal right to work in the country of the role.

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

• Health and wellness programs, including medical, dental, and vision coverage where applicable.

• Retirement and pension plans.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

• Opportunities for learning and development through structured training and career pathways.