Start Up Lead

Precision for Medicine is seeking a dedicated Start Up Lead to join our European team. This fully remote role focuses on the strategic planning and execution of global site start-up activities, ensuring that clinical trials are activated efficiently and in compliance with regulatory standards.

Key responsibilities

• Develop and implement activation readiness strategies to oversee site start-up delivery.
• Coordinate critical path planning, including IRB/EC and CA/MoH submissions, ICF customization, and IMP release requirements.
• Collaborate with cross-functional stakeholders to align operational goals and ensure timely milestone delivery.
• Act as a Subject Matter Expert, providing guidance and mentorship to team members on local regulations and start-up processes.
• Proactively identify risks to project timelines and execute effective mitigation strategies.

Requirements

• Bachelor’s degree in life sciences, nursing, or an equivalent combination of education and experience.
• Minimum of 5 years of experience in clinical site start-up, with specific experience in a lead or project management capacity within a CRO or pharmaceutical environment.
• At least 2 years of experience in managing project milestones, resources, and budgets.
• Strong knowledge of Good Clinical Practice (GCP), ICH guidelines, and local regulatory requirements.
• Excellent communication, leadership, and organizational skills with proficiency in electronic information systems.

What we offer

• The opportunity to work in a fully remote environment within a global organization.
• Professional development through mentorship and knowledge-sharing initiatives.
• Engagement in high-impact clinical research projects with a collaborative, international team.