GE HealthCare Strategic Category Lead Research Development 

United Kingdom, England 

247685598

As a Global Category Lead you will be responsible for supporting the coordination and management of all the procurement and sourcing activities for R&D for all aspects of drug product development, planned and current clinical trials globally.This position will require a working in partnership with Clinical Research Organisations (CRO) and suppliers, R&D, Program Management and functional leadership teams to create, develop and deliver the category strategy for R&D globally for GE Pharmaceutical Diagnostics’ (PDx).This position will also be responsible for ensuring we maximise the value obtained from partnerships with suppliers and includes supplier identification and selection, request for proposal (RFx), bid defenses, negotiating contracts, supplier performance metrics, and supplier oversight and governance.

Roles and Responsibilities

• As an integral member of the PDx Sourcing and R&D teams you will be responsible for developing and maintaining a lean and strategic approach to our CRO suppliers for the R&D.

• Ensure all activities with external suppliers are awarded and maintained in compliance with Good Clinical Practice, Standard Operating Procedures, and Corporate Policies, Guidelines and Standards.

• Responsible for maintaining internal collaboration between R&D, Product Management, Supply Chain & Direct material Sourcing (commercial launch planning), Quality and regulatory organisations within the PDx business.

• Execute agreed strategic sourcing strategy within the category and sub-categories to develop appropriate contracting frameworks to commercially capture the outputs, and manage all ongoing performance against live agreements.

• Responsible for supporting of new suppliers onto the Approved Supplier List for the current and future business needs, identifying gaps and identifying suitable suppliers to address the business need both regionally and globally.

• Support and manage the identification and selection process of clinical suppliers such as CROs, central labs, IVRS, Imaging, ePRO, etc., and support suppliers for R&D efforts such as regulatory, quality, etc..

• Generates Requests for Information (RFI), Request for Quotations (RFQ) and Requests for Proposals (RFP).

• Coordinates bid defenses and proposal review meetings and provides analysis to project teams.

• Contract lifecycle management: including support the drafting and management R&D contracts and change orders, including active negotiation of scope of work, payment terms and budgets.

• Works with the R&D Operations team, Clinical Project Directors, Portfolio Operations Manager and Contract Managers and or the Legal Team to support requirements and contractual needs and Change Orders.

• Works with Finance on budget/forecasting needs, cash flow, project budgets, etc.

• In partnership with the Quality and Supplier Quality organisations, ensures quality oversight of suppliers.

• Developing and maintain relationships with external partners, ensuring ongoing feedback and issue escalation is performed where needed.

• Measure’s supplier performance utilizing Key Performance Indicators (KPIs), Scorecard/Metric activities; and communicating feedback to the supplier, encourage adaptation on best practices across supplier types and development of continuous process improvements/ maintenance.

• Support supplier governance meetings and operating reviews.

• Develops effective partnerships with suppliers and internal stakeholders

• Identifies current trends in practices in the industry and develops a strategy around these trends that is then well communicated to internal stakeholders and implemented.

• Supports and contributes to complex functional or company initiatives and special projects as identified by executive management or business need.
  

Required Qualifications

• Bachelor’s degree (or equivalent) in a relevant subject, together with 5+ years of related industry experience.

• Experience in category management and sourcing along with defining and delivering effective category strategies which achieved significant cost transformations.

• Experience working within a preclinical or CRO environment.

• Experience in pharmaceutical research operations, compliance, clinical study execution and supplier management.

Desired Characteristics

• Strong Interpersonal and leadership skills.

• Established project management skills with the ability to document, plan, market, and execute projects.

• Strong business acumen and capacity to understand complex industry dynamics (supplier/partner/product relationships).

• Excellent communication skills and ability to interact and partner with all levels of management in the company.

• Project management skills to execute complex projects with multiple stakeholders.

• Fast learner: ability to learn enough of a complex industry and products to interact with highly technical experts, internal stakeholders and lead discussions, negotiations.

• Inclusiveness: ability to partner, support and listen and influence a wide array of internal and external

• Ability to energize, develop and build rapport at all levels within an organization.

Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration and support.