Global Director, Regulatory Sciences Program Management

PPG UK ProPharma Group MIS Ltd; Greater London; Ibrido; GBP 180.000 - 240.000; Tempo pieno

Descrizione del lavoro

ProPharma in Europe seeks a Senior Director, Program Management - Regulatory Sciences, Development, to oversee large, cross-functional client programs and drive delivery across regulatory, clinical, nonclinical, and CMC workstreams. You will lead a global portfolio, establish governance, and mentor Directors and Project Managers while advancing client relationships.

You will also support business development, uphold high standards of quality and operational excellence, and collaborate with

Competenze

• 15+ years of experience within pharmaceutical, biotechnology, CRO, or regulatory consulting environments.
• Minimum 8 years of experience leading complex cross-functional global development programmes.
• Experience leading regulatory, clinical, nonclinical, and CMC workstreams within pharmaceutical development programmes.
• Significant experience leading client-facing project and programme delivery within a consultancy environment.
• Proven track record of delivering high-impact projects within budget and timeline expectations.
• Experience with Smartsheet portfolio management, dashboard development, resource planning, and reporting.
• Experience overseeing Europe and Rest of World regulatory development programmes; global programme leadership preferred.

Mansioni

• Provide expert program and project management leadership across multiple complex client programs.
• Lead the development, implementation, and oversight of integrated program plans across regulatory, clinical, nonclinical, CMC, and other development functions and stakeholders.
• Strategically lead and deliver flagship client programs, ensuring efficient execution across all project phases.
• Establish program governance structures and lead cross-functional team meetings, executive reviews, and client steering committees.
• Ensure robust project planning, resource forecasting, risk management, issue resolution, and milestone tracking.
• Oversee project management activities in accordance with internal procedures, including budget monitoring, invoicing oversight, client liaison activities, and service growth opportunities.
• Lead key client relationships across multiple projects and service lines, ensuring consistently high standard of communication and project execution.
• Drive business growth initiatives, contributing to marketing activities and providing subject matter expert support to business development interactions.
• Lead and develop a team of Directors, Associate Directors, and Project Managers, including responsibility for coaching, performance management, resource allocation, and career development.
• Develop and implement program management standards, tools, templates, governance frameworks, and best operational practices.
• Stay informed of relevant program management methodologies, regulatory development practices, and project management technologies and contribute to industry workshops, trainings and calls for collaboration.
• Contribute to the ongoing improvement of internal regulatory processes and procedures.

Conoscenze

Program leadership

Stakeholder management

Business development

Cross-functional leadership

Executive communication

Formazione

Advanced degree (MSc, MBA, PhD, or equivalent)

Bachelor's degree in life sciences, healthcare, business, project management

Strumenti

Smartsheet

Descrizione del lavoro

ProPharma in Europe seeks a Senior Director, Program Management - Regulatory Sciences, Development, to oversee large, cross-functional client programs and drive delivery across regulatory, clinical, nonclinical, and CMC workstreams. You will lead a global portfolio, establish governance, and mentor Directors and Project Managers while advancing client relationships.

You will also support business development, uphold high standards of quality and operational excellence, and collaborate with