Director, Regional Site Liaison

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

📋 Description

• Reporting to the Executive Director of Clinical Partnerships & Engagement, the Regional Site Liaison (RSL) acts as a vital operational and scientific collaborator, bridging the gap between Jade and clinical trial sites.

• Develop and sustain robust relationships with Principal Investigators (PIs), site personnel, and Key Opinion Leaders (KOLs) to support ongoing and upcoming clinical trials.

• Plan and conduct in-person visits with PIs and site teams.

• Function as the primary contact for regionally assigned clinical trial sites across various programs at Jade.

• Offer protocol assistance to Investigators and site teams.

• Support and uphold site responsibility for meeting enrollment targets.

• Address site inquiries that fall outside the CRA scope promptly, escalating issues cross-functionally when necessary.

• Efficiently identify and resolve site-related challenges, providing exceptional service.

• Collaborate with internal teams and CROs to design and implement customized site engagement strategies.

• Collect and relay field insights to the internal Jade team, including performance metrics, KPIs, protocol feedback, and competitive trial activities.

• Deliver regular updates to Clinical Operations regarding site-level enrollment plans and performance to aid in the global enrollment strategy and ensure consistent trial execution.

• Ensure alignment with Clinical Operations, Clinical Development, Medical Affairs, and CRO partners (including CRAs).

• Assist with site initiation, activation, and ongoing trial conduct as requested by Clinical Operations, including co-monitoring with the CRA when appropriate.

⛳️ Requirements

• A Bachelor's degree in a related field is required; an advanced scientific or clinical degree is preferred.

• Over 10 years of clinical research experience (15 years for Director), ideally in Clinical Operations or Clinical Development (sponsor or CRO), with at least 4 years in a site-facing role (e.g., CRA, MSL, CTM).

• Strong comprehension of clinical trial protocols, processes, and compliant, non-promotional scientific exchange.

• Familiarity with FDA and ICH Guidelines, GCP, and clinical research standards.

• Exceptional interpersonal and communication abilities, capable of fostering effective relationships with both internal and external stakeholders, including CROs.

• Proven problem-solving skills with the capacity to escalate issues appropriately.

• Ability to work autonomously in a field-based position.

• Demonstrated effectiveness in a dynamic and fast-paced environment.

• Willingness to travel domestically or regionally (~ 50%); international travel may be necessary to support global programs.

🏝️ Benefits

• Jade Biosciences is proud to be an Equal Opportunity employer.

• All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.