• The Director in Clinical Operations will be dedicated to the profitable growth of the firm’s Healthcare Payer Provider optimization group. • This individual will lead the design, development and implementation of large integrated (operational, clinical and financial improvement) optimization programs resulting in high performing health care operations. • He or she will manage multi-work stream programs to timeline / scope / budget across the larger platform. • The Director will work with Guidehouse specialty areas and partner with the client to deliver robust solutions/outcomes to generate positive revenue for Guidehouse in areas including performance improvement, supply chain, workforce productivity, non-labor productivity, clinical operations, shared services and/or revenue management. • The Director will participate in and help direct nationwide business development and relationship management activities for Guidehouse Healthcare clients requiring optimization.

• Accountable for providing leadership, strategic, operational planning and oversight of clinical trial operations for 1-2 indications within one compound • Develop operational strategies for implementation of clinical studies regionally/globally • Ensure consistent and successful execution of operational aspects of regional and global studies • Provide leadership to Clinical Operations staff and to project teams for vendor evaluation and quality-based oversight • Benchmark, track and report operational and study metrics

• Deliver training, workflow support, and best-practice recommendations • Act as a trusted advisor to clinical leaders, care managers, physicians, and operational teams • Support change management initiatives by helping customers adapt workflows and processes • Assess the operating environment, identify critical success factors and risks • Monitor adoption, identify gaps, and recommend optimization strategies • Translate clinical operations workflow requirements into solution configurations • Advise hospital users on integrating Qventus product features • Lead clinical discovery sessions to capture requirements and align capabilities • Collaborate with product, engineering, and implementation teams • Review program performance data and create performance improvement plans • Stay up-to-date on clinical standards and represent the company at industry events

• Designing, planning, coordinating, and conducting all activities involved in initiating, monitoring, and completing clinical research studies in the clinical study sites • Acting as the primary contact and clinical trial expert for assigned study site personnel • Performing site assessments and qualification visits to support the site selection decision process • Developing and managing key study site documentation • Participating in and overseeing CRO delivery of site management activities • Validating product performance claims, supplying data for critical regulatory submissions • Executing site management activities for sponsored studies in assigned focus areas across all phases of study • Working in local and global study teams, including virtual teams