OverviewIn this role you lead cross-functional clinical projects within a general CRO, ensuring delivery on time, within scope and budget while upholding quality standards.
You act as the central coordinator among Clinical, Data Management, Regulatory, and other teams, driving performance and managing risks for sponsor programs.
You will maintain client relationships and support business development, contributing to large-scale clinical development efforts.
This position offers impact through shaping project delivery and maintaining a strong quality and compliance focus in a fast-paced environment.
ResponsabilidadesLead end-to-end project delivery ensuring timelines, scope, and budget are met
Manage cross-functional teams (Clinical, Data Management, Regulatory, etc.)
Identify, assess, and mitigate project risks
Develop and maintain detailed project plans and timelines
Act as the main point of contact for clients and stakeholders
Monitor project performance, including financials and profitability
Ensure compliance with internal SOPs and regulatory requirements
Allocate and manage project resources in collaboration with line managers
Report progress and escalate issues where needed
Support business development activities, including proposals and bid defenses
Mentor junior Project Managers when required
Requisitos principalesBachelor's degree in Life Sciences or similar
Minimum 5 years'
experience in project management (ideally within clinical research / CRO environment)
Strong knowledge of clinical trial regulations (e.g., ICH-GCP)
Proven ability to lead and manage cross-functional teams
Excellent communication and stakeholder management skills
Strong organizational and prioritization abilities
Financial and budget management experience
Solid problem-solving and decision-making skills excellent communication stakeholder management leadership