Jobs at Pfizer

Leads Pfizer’s global R&D Quality Management Systems, Validation, and Compliance program across sites. Responsibilities include managing cGLP, cGCP, and cGMP compliance; overseeing documentation, validation, training, audits, corrective actions, risk reviews, certifications, budgets, and continuous improvement. The role advises senior leaders, coordinates global stakeholders and vendors, manages multidisciplinary teams, and ensures consistent regulatory and quality-system implementation across pharmaceutical R&D facilities.

Leads strategic partnerships, negotiations, governance, and national agreements with Canadian retail pharmacy chains, banners, buying groups, and distributors. Translates agreements into execution models, analyzes account performance and channel insights, and collaborates with Legal, Compliance, Medical, Market Access, Operations, and Customer Solutions. Requires strong knowledge of pharmacy ecosystems, payer environments, healthcare systems, contracting, and partnership strategy, with frequent travel across Ontario and Western Canada.

Drives sales and territory growth for Pfizer’s migraine therapy by engaging healthcare providers in person and virtually. Develops territory call plans, builds customer relationships, uses reports and analytics to identify opportunities, educates providers on approved product and disease-state information, collaborates cross-functionally, and completes administrative responsibilities compliantly. The role requires travel throughout the assigned Southern Maryland territory and occasional overnight stays.

Leads Pfizer’s global customs governance and compliance framework, including Belgian Authorized Economic Operator status, internal controls, customs valuation reporting, audits, continuous improvement, and stakeholder partnerships. Provides technical expertise in customs law and operations while implementing standardized, automated workflows aligned with GDP, GMP, and local regulations. Oversees talent development, performance standards, budgeting, and strategic customs initiatives across global operations.

Manages archiving completeness and transport-document compliance for global pharmaceutical logistics shipments. Designs and improves compliance processes, oversees outsourced service providers, coordinates issue resolution, tracks KPIs, and leads stakeholder forums and continuous-improvement initiatives. Partners with Digital, Quality, Indirect Tax, Transportation, and external providers to recover documentation gaps and ensure compliance with EU GDP/GMP and applicable local regulations, including FDA and Japanese requirements. Promotes automation, AI-enabled tools, risk management, and adherence to SOPs and work instructions.

Manages, monitors, and closes assigned clinical trial sites, ensuring patient safety, protocol compliance, data quality, regulatory adherence, and timely study delivery. Responsibilities include site relationship management, recruitment support, onsite and remote monitoring, adverse event follow-up, investigational product oversight, issue resolution, audit and CAPA support, reporting, and database release. The role also mentors clinical research associates, supports site activation and feasibility activities, and participates in process improvement initiatives.

Promotes Pfizer oncology products to healthcare providers, institutions, and organized customers. Educates healthcare professionals on appropriate product use, develops strategic account and territory plans, builds relationships with key opinion leaders, assesses customer needs, overcomes access barriers, and generates demand. The role requires strong pharmaceutical or oncology healthcare experience, scientific communication skills, business acumen, digital proficiency, and the ability to collaborate across a matrixed organization.

Manages, monitors, and closes assigned clinical trial sites from initiation through database lock. Ensures patient safety, protocol compliance, data quality, regulatory adherence, recruitment progress, investigational product accountability, and timely issue resolution. Serves as the primary site contact, conducts onsite and remote monitoring, supports audits and CAPA activities, trains site personnel, resolves data queries, and collaborates with investigators, vendors, drug safety teams, and study stakeholders. The role also mentors Clinical Research Associates and contributes to process improvement initiatives.