Snr Safety Project Lead (Lifecycle Safety)

Location: Frankfurt, Hesse, Germany

Company

hirify.global provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

• Manage customer interfaces, communications, deliverables, timelines, scope, quality, and financial activities for assigned lifecycle safety projects.
• Lead clinical trial and post-market safety service delivery, coordinating internal teams, customers, oversight groups, and integrated partners.
• Design safety solutions for new business opportunities, including operational assumptions, budgets, customized content, strategy, and pricing.
• Support proposals, sales presentations, bid defenses, project transitions, and strategic initiatives across the commercial lifecycle.
• Oversee project start-up, identify delivery risks, implement mitigation measures, and contribute to audits, inspections, and corrective action plans.
• Provide project status updates, financial analysis, revenue recognition support, invoicing coordination, and change-order management.

Requirements

• Life sciences degree or another directly related qualification.
• At least 3 years of lifecycle safety experience, such as pharmacovigilance, CEVA, medical information, safety publishing, or risk management, including project management experience.
• Knowledge of global, regional, and local clinical research regulations, including GCP, ICH guidelines, and hirify.global standard operating procedures.
• Strong planning, prioritization, organization, delegation, presentation, reporting, negotiation, decision-making, and problem-solving skills.
• Ability to manage multiple projects and competing priorities independently while maintaining effective relationships with customers and coworkers.
• Knowledge of business operations, financial analysis, tactical planning, and budgeting.

Culture & Benefits

• Cross-functional collaboration with global management, sales, proposals, quality assurance, customers, and integrated partners.
• Opportunities to contribute specialist expertise as a subject matter expert on departmental and global initiatives.
• Work focused on accelerating the development and commercialization of medical treatments and improving patient outcomes.