Position is virtual and will be working on UK / US hours. 8PM to 5am PH Time

Qualifications:

• Bachelor's degree with at least 5 years of experience; OR a master's degree with at least 3 years of experience; OR a PhD with 0+ years of experience; OR as associate's degree with 8 years of experience;
• Bachelor’s degree in supply chain, scientific discipline, project management, or business administration
• 5+ years of experience in pharmaceutical or biotech project management and cross-functional team leadership
• Demonstrated understanding of pharma quality and regulatory framework.
• Demonstrated success in matrix team environments with strong collaboration and accountability
• Excellent English communication skills (written and verbal)
• Proficiency in Microsoft Office tools, including MS Project and Office Timeline-Pro
• Flexibility to work across global time zones

Skills:

• Knowledge of Good Manufacture Practice (GMP), Good Clinical Practice (GCP), and regulatory frameworks
• Proven ability to manage complex clinical development programs and multiple studies
• Background in drug development or clinical study logistics (e.g., randomization, packaging, labeling, distribution)
• Strong budgeting and forecasting skills, including supply demand planning
• Skilled in stakeholder alignment, negotiation, and performance measurement
• Experience presenting at conferences or large forums

Preferred:

• Business, scientific, or technical degree and/or coursework with specific training in supply chain management preferably in pharmaceutical industry.
• Training or experience in safety, regulatory, medical and/or clinical supply chain, delivery and/or implementation.
• In-depth understanding of pharmaceutical business processes and regulations, guidelines, and industry standards for compliance.
• Proven ability to effectively develop, communicate, and execute project plans with multiple stakeholders.
• Previous continuous improvement experience considered a plus.
• Strong interpersonal skills with a demonstrated ability to manage stakeholders in different levels of technical and business roles.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.