POSITION SUMMARY

We are seeking a motivated and collaborative Medic - EU to join our growing clinical development team. This full-time role will support global clinical trials across multiple programs, working closely with cross-functional teams, investigators, CROs, and study sites. The ideal candidate is a physician (MD or equivalent) with clinical research experience who thrives in a fast-paced, hands-on environment and is passionate about advancing new therapies.

ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.

Strategic Objectives

· Support the execution of the global clinical development strategy with high-quality trial conduct.

· Build collaborative relationships with external investigators, CROs, and cross-functional internal teams.

· Provide clinical insights to optimize patient recruitment and retention.

· Contribute to ongoing safety signal detection, risk mitigation, and data integrity oversight.

· Support future protocol amendments, expansion cohorts, and potential new development programs.

Operational Objectives

· Ensure protocol compliance and patient safety through active medical monitoring.

· Serve as a first-line medical resource for investigators and site queries.

· Collaborate with clinical operations to monitor enrollment progress, resolve operational issues, and ensure trial timelines are met.

· Support training of site personnel and CRO staff on protocol requirements and safety procedures.

· Contribute to clinical trial quality assurance, data review, and inspection readiness efforts.

· Attendance at scientific and medical conferences.

· Assist with analytical support of clinical trial data, including gathering, analyzing, reviewing, interpreting, and providing preliminary assessments and recommendations.