Clinical Trial Liaison

This is a fully remote position, open to applicants in Texas.

📋 Description

• Oversee the complete range of investigator engagement, from identification and qualification to enrollment, database lock support, and study closeout.

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

• Forge strategic relationships with investigators across various trials and therapeutic domains.

• Develop customized recruitment strategies and identify new opportunities to reach potential patients, thereby expediting enrollment.

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

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

• Utilize performance metrics to foresee potential issues and ensure progress towards clinical milestones.

• Promote inspection readiness across all sites.

• Collaborate with cross-functional teams and vendor partners to overcome operational challenges.

• Stay informed about local treatment paradigms and standards of care for effective country/site selection and protocol localization.

• Provide oversight and ensure quality assurance for vendor monitoring activities.

• Lead Post-Marketing Safety Studies when applicable.

• Build a portfolio of strategically aligned investigators.

• Enhance the investigator experience by acting as a scientific partner.

• Perform data-driven site prospecting and prioritization.

• Serve as a liaison among field teams, vendors, and investigators.

• Collaborate with field team colleagues to improve enrollment results and strengthen investigator relationships.

⛳️ Requirements

• Bachelor’s degree or equivalent; a strong preference for candidates from scientific, clinical, or health-related disciplines.

• At least 5 years of experience in clinical research or the pharmaceutical industry, with direct interaction or collaboration with healthcare professionals (HCPs) and clinical sites.

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

• Experience in oncology is essential, with a preference for Breast/Gyn experience.

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

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

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

• Retirement and pension plans.

• Life assurance and disability coverage.

• Employee assistance programs and wellness resources.

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