OverviewAs a Project Director, you lead global oncology clinical trial programs, overseeing study portfolios and cross-functional teams to ensure on-time, within-scope delivery.

You partner with clients to align on goals, drive process improvements, and maintain high-quality execution across studies.

You shape trial strategy, risk management, and change management while supporting business development and senior leadership.

This role offers remote work from several EU countries and wide collaboration with senior stakeholders.

Compensaciones / Beneficiosfully remote role work-life balance supportive and collaborative environment travel for bid defenses as required opportunity to mentor and develop staff

ResponsabilidadesAct as primary client liaison and lead proposal activities and presentations

Oversee end-to-end trial management across portfolios with consistent execution

Provide direction to project managers on establishment, planning, initiation, procurement, execution and closeout

Manage study budget, identify out-of-scope work, drive change orders, and ensure financial health

Develop robust project plans with timelines, risk mitigation, and quality controls

Ensure quality management for projects (eTMF readiness, CAPA/quality plans)

Establish and monitor tracking metrics; prepare status updates for clients and senior management

Lead internal and client meetings; set expectations and drive study-level strategies





Oversee cross-functional teams and ensure effective collaboration across functional areas

Communicate protocol/study issues to sponsor and precision management and implement corrective actions

Conduct formal presentations to diverse audiences including bid defenses

Ensure study-specific training and compliance throughout the project

Support business development and travel for bid defense activities

Mentor associate/project managers and contribute to SOP updates

Provide performance feedback and drive corrective actions as needed

Travel domestically and internationally as required

Requisitos principalesMinimum 8 years of clinical research or equivalent experience

Minimum 5 years direct project management experience

Proficiency with Microsoft Office, Microsoft Project, eTMF, EDC and CTMS

Excellent communication, interpersonal, organizational, and customer service skills

Experience managing highly complex and general studies or portfolios

Strong knowledge of ICH-GCP and company SOPs

Ability to lead cross-functional teams and manage stakeholders across regions

Independent planning, risk, and change management capabilities

Ability to travel as needed

Strong communication and presentation skills

Customer-focused mindset

Collaborative leadership

Microsoft Office Suite (Outlook, Word, Excel, PowerPoint)

Microsoft Project eTMF

📌 Project Director - España (Valladolid)
🏢 Precision Medicine Group
📍 Valladolid