Associate Director, EGME Lead Mexico

Job Description Summary

Provides contracting life cycle management and business solutions optimizing operational expertise to US MA US Medical Affairs, partnering with all areas in the end-to-end planning process and execution. Responsible for managing cross-functional teams in evidence generation and medical excellence requiring alignment of team goals with organizational objectives, fostering collaboration, ensuring quality and compliance, and encouraging innovation. It also includes engaging stakeholders, managing resources efficiently, and monitoring team performance to achieve strategic outcomes.

Job Description

This role is based in Mexico City, Novartis is unable to offer relocation support for this role : please only apply if this location is accessible for you.

Key Responsibilities

Contract Life Cyle Management : Implements best-in-class contract management processes and tools in the day-to-day practice. Provides continuous feedback from the execution / implementation to align best practices with business needs. Reports on set cadence tracking metrics and suggested process improvements.

Contract : Authors, negotiates, executes, and manages the contractual documents needed to affect the research projects proposed and approved by US MA. Ensures contracting activities, as applicable, adhere to Internal SOP and WP processes, and Corporate Integrity. Produces final contracts / amendments and secures all necessary company approvals including SOX compliance to facilitate execution of said agreements. Ensures appropriate contractual Amendments and Addendums are in place. Assists US MA CBS team in defining scopes of work (SOW) and preparing project specific milestone payment schedules for both original contracts and amendments.

Collaborator : ability to collaborate with US Legal and Patent departments to Lead and to answer questions regarding contract terms, scopes of work, pricing, and payment schedules within the framework of the US legal and compliance requirements.

Lead / Manage : Facilitates / coordinates the process as the lead for NOCC and Evidence Generation and Medical Excellence Associates, inclusive of workload, strategies and priorities by bringing insights from the execution and delivery of tactics.Manage cross functional reports from Clinical Supply Management, Medical Operations and Contracts and Business Solutions

Excellence in Business Solutions execution : Coordinates / tracks contract and scope driven milestones and overall CLC and business solutions progress. Provides program management support for selected tactics based on complexity and relevance to harmonize team’s workload and integrate with ED CBS for the overall deliverables. Continuously evaluates to find improvement opportunities and improve strategic and tactical plans.

Budget management : Ensures FMV and Schedule As abide by US Laws, Regulations and adhere to all local process, aligning milestone deliverables with cost and payment to ensure minimal deviations from local guidelines and standards. Proactive evaluation and identification of risks / opportunities. Facilitates process to re-prioritize and define mitigative actions.

Stakeholder management & communications : Engages with multiple stakeholders within Medical Affairs and across the organization to ensure the delivery of quality, timely and cost-effective external resources to support US Medical Affairs. Partners with Executive Director of EGME to lead the process of developing tactical plans aligned to strategies and priorities. Supports projects and initiatives to ensure the workload is prepared to successfully respond to the changing needs and requirements of our business partners.

Knowledge management : US laws and regulations associated with contract language regarding US Phama regulations to GxP, with specific knowledge of Phase 1-IV, Registries, and IIT studies with secondary knowledge including, but not limited to, research collaborations, MAPS, consultancy agreements and confidentiality agreements, that may shift based on evolving business needs.

Direct Management Responsibility : Oversee and mentor direct reports, providing guidance, performance feedback, and professional development opportunities to ensure team success.

Minimum Requirements

Bachelor’s degree in business / legal field required; Advanced degree preferred.

Minimum 10+ years of experience in the Pharmaceutical Industry and Minimum 7+ years in a Contracting Function.

Thorough understanding of US clinical trial conduct and regulation.

Excellent understanding of contracts and financial terms (including legal understanding of terms and conditions).

Proven record of accomplishments that demonstrate strong contract management, analytical and multitasking skills for business solutions.

Possess strong internal and / or external influence to achieve business & operational objectives. Excellent interpersonal skills (team player). Proven negotiation skills.

Demonstrated willingness to make decisions and to take responsibility. Must be able to work independently and be fully agile in adapting to evolving business needs to fulfill secondary requirements.

Experience managing and negotiating payment terms / budgets.

Strong English written, oral & presentation skills, with an ability to make professional and credible first impressions with internal and external customers.

Ability to manage 6-12 direct reports

Commitment to Inclusion

Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Novartis is committed to work with and provide reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to tas.mexico@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

Skills Desired

Budget Management, Clinical Research, Clinical Trial Protocol, Clinical Trials, Coaching, Cross-Functional Teams, Data Analysis, Learning Design, Lifesciences, Risk Management, Risk Monitoring

#J-18808-Ljbffr