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AtaiBeckley · 1 week ago

Clinical Development Liaison

United States

Full-time

Remote

Senior Level

5+ years exp

AtaiBeckley is seeking a Clinical Development Liaison to act as a key link between clinical research sites and internal study teams. This role involves driving site activation, enrollment support, and operational delivery while building strong relationships with research sites and supporting trial oversight activities.

BiotechnologyLife ScienceMental HealthNeuroscienceTherapeutics

Growth Opportunities

Responsibilities

Oversee high-quality Site Initiation Visits (SIVs) and co-monitoring visits conducted by the CRO, ensuring compliance with protocol, GCP, and regulatory requirements

Develop and execute site engagement strategies to drive enrolment, including investigator meetings, site visits, and tailored site support initiatives

Support first-patient dosed milestones, provide on-site training reinforcement, and enhance site motivation through targeted engagement efforts

Implement site appreciation tactics such as team meetings, investigator touchpoints, and recognition efforts to strengthen relationships

Identify and proactively mitigate site-level operational challenges, escalating issues as needed

Collaborate with cross-functional teams (e.g., medical, feasibility, and operations) to ensure aligned site support strategies

Act as a key contributor to trial management activities, supporting Clinical Project Managers (CPMs) in oversight of study execution

Track and assess site and CRO performance metrics, contributing to risk mitigation strategies

Assist in developing and maintaining study plans, including site monitoring plans and enrolment tracking

Participate in vendor and CRO oversight activities, ensuring alignment with study timelines and quality expectations

Support clinical study documentation, including review of monitoring reports, study logs, and essential document management

Contribute to study meeting preparation, including investigator meetings, internal study team calls, and governance meetings

Collaborate with regulatory, safety, and data management teams to ensure seamless study execution

Qualification

Clinical research experienceGCP knowledgeICH guidelines knowledgeSite engagement strategiesClinical trial managementProblem-solvingOrganizational skillsCommunication skillsCollaboration skills