Associate Director, Clinical Site Contracting (Remote)

Company Description

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

Job Description

The Associate Director, Site Contracting (AD) acts as the first line of contact for all R&D business partners and provides leadership to drive and implement the clinical strategy with a high level of expertise for multiple compounds across a large portfolio or therapeutic area (TA). This position collaborates and partners with Clinical Development Operations (CDO), finance, legal, OEC and other internal stakeholders to deliver services / clinical contracts for clinical trials leading strategy across the function to ensure key milestones are met or exceeded. The AD acts as line manager for multiple direct and indirect reports, who may be located across multiple countries and/or regions.

Responsibilities

In addition to the above, the position may also be required to lead on specific areas of focus such as:

• Measurement & communication of functional performance via KPIs, & strategic planning & implementation of targeted improvements indicated.
• Leadership, Management & oversight of Service Provision (e.g. CRO flexible resource) deliverables across the function.
• Lead & oversee CSA Budget and Contract delivery for TA, project, or country.
• Compliance & Training liaison/lead for TA or region.
• Systems development & regional implementation SME.
• Compliance Manager for FMV process and compliance with AbbVie SOPs including but not limited to purchasing, R&D, payments, etc.
• Influences and strategically manages the linkages across multiple functional areas, including quality, CDO, legal, finance and OEC to drive the successful implementation of the R+D strategy within the global clinical trial environment. Leads the strategy for workload mana