Associate Director_cFSP RSU_EMEA

Location: Madrid, Spain

Company

Global provider of clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

• Direct Site Activation operations for an assigned EMEA sub-region or functional area.
• Develop strategic goals, implementation plans, resource plans, and success measures with senior management.
• Manage staff, hiring, performance evaluation, professional development, employee relations, and human resources actions.
• Lead operational delivery, process improvement, quality initiatives, and service offerings to meet customer expectations.
• Evaluate workload, quality, budget, and resourcing metrics, and guide corrective fiscal action plans.
• Collaborate with clients and cross-functional leaders to resolve project challenges and improve outcomes.

Requirements

• Bachelor's degree in healthcare or another scientific discipline preferred, or an equivalent combination of education, training, and experience.
• At least 10 years of clinical trials experience, including 6 years in a leadership capacity.
• Full knowledge of the drug development process, applicable regulations, SOPs, and corporate standards.
• Knowledge of GCP/ICH guidelines, regulatory requirements, budget management, and resourcing.
• Strong ability to lead and motivate teams, coordinate processes independently, and manage operational priorities.
• Strong knowledge of Microsoft Office, email applications, and medical terminology.

Culture & Benefits

• Work within a global clinical research and healthcare intelligence organization.
• Collaborate with senior management, clients, and functional leaders across Site Activation operations.
• Participate in strategic, quality, and process improvement initiatives.
• Work in an environment focused on diversity, inclusion, belonging, and innovation in healthcare.