Lifecycle Safety Program Lead

IQVIA Argentina; Durham (NC); On-site; USD 86,000 - 215,000; Full time

Job summary

IQVIA in Durham, NC seeks a Lifecycle Safety program leader responsible for management and service delivery excellence across large regional and global projects. You will guide customer interfaces, oversee planning, budgets, and quality, and work with cross-functional teams to deliver integrated safety solutions.

The role requires 4–6 years in clinical research within CRO/pharma, strong leadership, budgeting, and communication skills; familiarity with GCP/ICH and IQVIA SOPs; and the ability to

Qualifications

• 4 to 6 years of clinical research experience in CRO or pharmaceutical setting, including Lifecycle Safety.
• Strong knowledge of global/regional/local clinical research requirements (GCP/ICH) and IQVIA SOPs.
• Willingness to expand knowledge across Lifecycle Safety service lines and develop new skills.
• Excellent team leadership, conflict management, and delegation abilities.
• Proven ability to manage multiple projects and priorities in a matrix environment.

Responsibilities

• Lead customer-facing lifecycle safety programs, ensuring delivery against timelines and budgets.
• Oversee project planning, scope management, quality, and financial performance.
• Serve as Safety SME and primary liaison among customers, executives and partners.
• Collaborate with sales/proposals to tailor responses and grow the business.
• Provide leadership for project startup through transition to service delivery and renewal.

Skills

Leadership

Project management

Communication skills

Budgeting

Stakeholder management

Negotiation

Education

Bachelor's Degree Health Science

Job description

IQVIA in Durham, NC seeks a Lifecycle Safety program leader responsible for management and service delivery excellence across large regional and global projects. You will guide customer interfaces, oversee planning, budgets, and quality, and work with cross-functional teams to deliver integrated safety solutions.

The role requires 4–6 years in clinical research within CRO/pharma, strong leadership, budgeting, and communication skills; familiarity with GCP/ICH and IQVIA SOPs; and the ability to