Clinical Trial Liaison

This is a fully remote position, open to applicants in North Carolina, +3 more states.

📋 Description

• Oversee the engagement of clinical investigators, from initial identification and qualification to enrollment, database lock support, and study closeout.

• Act as a scientific ambassador for clinical trials, clarifying protocol intent, scientific rationale, and patient eligibility criteria.

• Develop and maintain strategic relationships with investigators across multiple trials and therapeutic domains.

• Collaborate in the creation of tailored recruitment strategies and identify avenues to reach new patients and expedite enrollment.

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

• Lead the strategy and risk planning at the site level for enrollment and data delivery.

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

• Promote inspection readiness across all sites.

• Work with cross-functional teams and vendors to eliminate operational obstacles.

• Leverage knowledge of local treatment paradigms and standards of care for country/site selection and protocol adaptation.

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

• If applicable, manage Post-Marketing Safety Studies end-to-end, ensuring compliance with local regulations.

• Develop a portfolio of strategically aligned investigators and enhance their overall experience.

• Conduct data-driven site prospecting and prioritization.

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

• Represent Investigator Engagement with regulatory bodies, ethics committees, and national research organizations as needed.

• Influence the clinical trial environment and align regional initiatives with overarching clinical development goals.

⛳️ Requirements

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

• A minimum of 2 years of relevant experience in the clinical or therapeutic area of Oncology.

• An advanced degree in a scientific or clinical discipline (PharmD, PhD, MD, or MSc preferred).

• Strong understanding of Good Clinical Practice (GCP), clinical development and operations, and the trial lifecycle.

• Proven knowledge of the therapeutic landscape and standards of care, with the capacity to apply this expertise in decision-making.

• Demonstrated capability to establish credibility and influence the healthcare professional community through scientific knowledge and relationship-building.

• Current experience in Oncology is essential.

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

• Willingness to travel up to 60% of the time.

🏝️ 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 advancement pathways.