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 the identification and qualification stages through to enrollment, database lock, and study closeout.

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

• Establish and nurture strategic relationships with investigators across various trials and therapeutic areas.

• Collaborate on recruitment strategies that are in line with site capabilities, patient demographics, and study goals.

• Discover new avenues for reaching potential patients and enhancing enrollment, including innovative site models and community-based research efforts.

• Gather and amplify site insights to enhance feasibility, protocol design, and the overall conduct of studies.

• Direct site-level strategies and risk management for enrollment and data delivery.

• Utilize performance metrics to foresee challenges, intervene as necessary, and ensure progress towards clinical milestones.

• Ensure sites are prepared for inspections.

• Work alongside internal teams and vendors to overcome operational obstacles.

• Leverage knowledge of local treatment paradigms and standard care practices to guide country/site selection and protocol adaptation.

• Supervise vendor monitoring and quality assurance, proactively escalating any risks.

• Where applicable, take charge of the comprehensive management of Post-Marketing Safety Studies in accordance with local regulations.

• Build a network of strategically focused investigators who prioritize client trials.

• Deliver a responsive and knowledgeable experience to investigators as a scientific partner.

• Coordinate with Medical, Clinical, Study Delivery, field teams, vendors, and investigators to ensure alignment of priorities and address challenges.

• Conduct data-driven site prospecting and prioritization.

• Facilitate scientific and therapeutic dialogues with site personnel.

• Ensure alignment, shared objectives, and knowledge sharing among field teams, vendors, and investigators.

• Enhance investigator relationships, site experiences, and enrollment results.

⛳️ Requirements

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

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

• Experience in direct interaction with or collaboration with healthcare professionals and clinical sites.

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

• Experience in immunology is mandatory.

• 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.

• 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.

• Travel opportunities of up to 60–80% during peak periods.