Vor Bio is hiring a Clinical Site Liaison

Vor Bio is hiring a Clinical Site Liaison to serve as a key field-based extension of our Clinical Operations team. In this role, you will build strong relationships with investigative sites, ensure high-quality study execution, and provide proactive support to facilitate communication and remove operational barriers.

What You'll Do

• Serve as the primary point of contact for assigned clinical trial sites, fostering strong, collaborative relationships.
• Conduct regular check-ins (virtual or on-site) to assess site needs, enrollment progress, and operational challenges.
• Ensure sites have timely access to study materials, training, and updates.
• Monitor enrollment performance and partner with sites to identify recruitment opportunities and barriers.
• Support site-level feasibility, start-up activities, and readiness assessments.
• Provide guidance on protocol requirements, visit schedules, and operational expectations.
• Reinforce adherence to protocol, GCP, and study-specific procedures.
• Identify and escalate potential quality issues, data inconsistencies, or protocol deviations.
• Collaborate with CRAs, Clinical Operations, and Medical Monitoring to ensure timely issue resolution.
• Act as a conduit between sites and internal teams (Clinical Ops, Medical Affairs, Data Management, Safety).
• Share site insights to inform study planning, risk mitigation, and operational decision-making.
• Support vendor coordination (central labs, imaging, ePRO, etc.) as needed.
• Participate in investigator meetings, site trainings, and study team calls.
• Contribute to development of site-facing tools, communications, and best practices.
• Maintain accurate documentation of site interactions and follow-up actions.

What We're Looking For

• Bachelor’s degree in life sciences or a related field.
• 8 years of experience in clinical research (Clinical Study Manager, CRM or CSL or Clinical Trial Lead) for Associate Director level.
• 6 years of experience in clinical research (Clinical Study Manager, CRM or CSL or Clinical Trial Lead) for Senior Manager level.
• Strong understanding of clinical trial operations, GCP, and site workflows.
• Excellent communication, relationship-building, and problem-solving skills.
• Ability to travel to investigative sites as needed (approximate travel 85%).

Nice to Have

• Advanced degree.
• Experience in small biotech or fast-paced clinical environments.

Team & Environment

You will be a field-based extension of the Clinical Operations team, working independently to support investigative sites.

Benefits & Compensation

• Senior Manager: $175,000-$190,000 per year.
• Associate Director: $195,000-$210,000 per year.
• Comprehensive health coverage.
• Flexible paid time off.
• Generous parental leave.
• Competitive 401(k).
• Education assistance.
• Wellness resources.
• Financial security.

Work Mode

This is a local-country, field-based position requiring significant travel to investigative sites.

As an equal opportunity employer, we at Vor Bio know that diversity inspires innovation, inclusiveness, and creativity. We invite you to come as you are. All applicants will be considered for employment agnostic to race, age, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.