Clinical Trial Liaison

This is a fully remote position, open to applicants in Illinois, +4 more states.

📋 Description

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

• Act as a scientific ambassador for clinical trials, clearly communicating protocol intent, scientific rationale, and patient eligibility criteria to investigators.

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

• Enhance enrollment through customized recruitment strategies that align with site capabilities, patient demographics, and study goals.

• Identify avenues for reaching new patients, expediting enrollment, and maximizing impact at key sites.

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

• Lead strategic planning and risk assessment at the site level concerning enrollment and data delivery.

• Utilize performance metrics to foresee challenges, take action, and ensure progress towards clinical milestones.

• Promote continuous readiness for inspections across all sites.

• Work in collaboration with functions and vendor partners to address operational challenges.

• Leverage knowledge of local treatment paradigms and standards of care to influence site and protocol selection.

• Supervise and ensure quality assurance for vendor monitoring while proactively escalating risks.

• When applicable, manage Post-Marketing Safety Studies from start to finish in accordance with local regulations.

• Develop a portfolio of strategically aligned investigators.

• Provide a knowledgeable and responsive scientific partnership to investigators.

• Collaborate with Medical, Clinical, Study Delivery, field teams, vendors, and investigators to align priorities and tackle challenges.

• Conduct data-driven site prospecting and prioritization.

• Maintain scientific fluency and therapeutic knowledge in interactions with site personnel.

• Foster alignment, shared objectives, and knowledge transfer among field teams, vendors, and investigators.

• Enhance relationships with investigators, improve site experiences, and boost enrollment outcomes.

⛳️ Requirements

• Bachelor’s degree or equivalent; strong preference for degrees in scientific, clinical, or health-related fields.

• At least 5 years of experience in clinical research or the pharmaceutical industry.

• Experience in direct interactions with healthcare professionals and clinical sites.

• Willingness to travel up to 60–80% during peak periods.

• Experience in immunology is required.

• Must reside in Indiana, Kentucky, North Carolina, Michigan, Ohio, or Illinois.

• Legal authorization to work in the country where the position is based.

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

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

• Retirement and pension schemes.

• Life assurance and disability coverage.

• Employee assistance programs and wellness resources.

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