Role Description The Senior Clinical Pharmacist serves as a subject matter expert for the Part D Stars measures as well as other medication related issues including navigating the pharmacy benefit. This role will foster and manage relationships with internal and external partners to produce positive health outcomes and solid star performance for the plan. Work Schedule (40 hrs./week): - Monday – Friday 8am – 5pm local time with flexibility based on travel requirements - Local, state, and national travel up to 25% of the time based on business needs - Flexibility to telecommute from anywhere within the U.S. Primary Responsibilities: - Provide clinical pharmacy advice and guidance on quality of care programs including HEDIS and CMS Stars programs - Develop and train best practices to improve medication adherence and medication related measure gap closures - Interpret pharmacy programs to write clinical guidelines, job aids, and decision trees - Write and collaborate on member/provider collateral materials for pharmacy programs - Work on program implementation teams and contribute to business process design and systems set up, troubleshooting, and updates - Review programs for compliance with state, federal, and CMS regulations and recommend remediation - Monitor impending legislation for potential impact on current and future programs - Analyze data and prepare management summaries related to work stream results, performance management results, audit results, CMS reporting, and client reporting - Perform quality audits, determine performance gaps and root causes, prepare reports and collaborate on remediation - Examine, evaluate, and provide recommendations to evolve and enhance clinical pharmacy programs and best practices Qualifications - High School Diploma/GED - Current and unrestricted pharmacist licensure in State of residence - 5+ years of experience working as a Licensed Pharmacist within varied practice settings - 5+ years of experience and/or knowledge of Medicare Part D, Medicaid, and/or commercial - 1+ year of experience delivering presentations to large audiences - Intermediate level of proficiency with navigating MS Office and Windows-based environment - Ability to travel up to 25% of the time Preferred Qualifications - Doctor of Pharmacy (PharmD) - Residency and/or Board Certification (ie: BCPS, BCACP, BCGP) - Clinical quality experience (ie: HEDIS, Stars, NCQA) - Experience with Medicare Advantage - Experience working closely with and influencing providers - Experience teaching, training, and presenting accurate clinical information verbally to a variety of audiences Soft Skills - Excellent written, verbal and presentation skills Benefits - Comprehensive benefits package - Incentive and recognition programs - Equity stock purchase - 401k contribution (all benefits are subject to eligibility requirements) Compensation The hourly pay for this role will range from $112,700 to $193,000 per annum based on full-time employment. Pay is based on several factors including but not limited to local labor markets, education, work experience, certifications, etc. Application Deadline This will be posted for a minimum of 2 business days or until a sufficient candidate pool has been collected. Job posting may come down early due to volume of applicants.

• Manage and oversee local trial management services throughout the study • Execution of local milestones from feasibility through study close out • Resourcing of country-level roles in collaboration and agreement with the study Functional Manager (FM) • Close collaboration with assigned Local Trial Manager(s), Lead Site Manager, Site Managers, Clinical Trial Associates, and Site Contract Managers • Inspecting Readiness and AQR at the country level • Country level ad hoc meetings to address unexpected circumstances that might impact country or study level deliverables • Provide updates, discuss hurdles, timelines/resources, and potential risks with the study FM • Assist with necessary documentation for leadership

• Serves as a statistical department resource, mentors biostatisticians on job skills, and oversees or develops training plans or materials for Biostatistics associates. • Conducts training sessions, or otherwise trains new hires and enhance the skills of existing personnel. • Directs the activities of other biostatistics personnel on assigned projects to ensure timely completion of high quality work. • Provides independent review of project work produced by other biostatisticians in the department. • Provides support across all statistical tasks during the lifecycle of the project, from protocol to CSR. • Prepares or oversees the preparation of Statistical Analysis Plans (SAPs), including development of well-presented mock-up displays for tables, listings, and figures. Collaborates with sponsor, if required. • May be responsible as Lead Biostatician for the statistical aspects of the protocol, generation of randomization schedule, and input to the clinical study report. • Creates or reviews programming specifications for analysis datasets, tables, listings, and figures. • Reviews SAS annotated case report forms (CRFs), database design, and other study documentation to ensure protocol criteria are met and all data is captured as required to support a high quality database and the planned analysis. • Implements company objectives, and creates alternative solutions to address business and operational challenges. • As biostatistics representative on project teams, interfaces with other departmental project team representatives. • Preparing in advance for internal meetings, contributing ideas, and demonstrating respect for opinions of others.

• Responsible for site management oversight, clinical monitoring and central monitoring deliverables with a focus on patient safety, protocol/GCP/regulatory compliance and data integrity. • Oversees site interactions post activation through site closeout. • May be responsible for identification of critical data and process, protocol execution risks and risk mitigations related to completion of the Risk Assessment and Categorization Tool (RACT). • Reviews the study scope of work, budget and protocol content and ensures the clinical project team (CRAs/Central Monitors) is aware of the contractual obligations and parameters. • Uses prior clinical experience, operational data, metrics and reports to identify risks to clinical trial management deliverables. • Escalates to the project manager any risks to clinical trial management deliverables (timeline, quality and budget) and any activities and requests which are out of contracted scope. • Employs strategic thinking and problem-solving skills to propose and implement risk mitigations. • Participates and presents in key meetings such as Kick Off Meeting. • Serves as an escalation point for communications with investigator site staff and may be required to interact on the phone or in person with principal investigators or other site staff members. • This may include accompanying CRA team members to sites for observation or conflict resolution. • Collaborates with other functional leaders such as Study Start Up, Patient Recruitment and Data Management to coordinate delivery handoffs and meet expected study milestones such as site activation targets, enrollment targets and database lock timelines. • Reviews and provides feedback on other functional plans (e.g. Data Management Plan, Communication Plan) as they relate to the clinical trial management activities. • Responsible for development and ongoing maintenance of clinical study tools and templates, including the Clinical Monitoring Plan. • Ensures CTMS, dashboards and other systems are set up and available for use by the clinical team, including overseeing user acceptance testing (UAT) as needed. • Ensures access and audit trail reviews are conducted as required. • Coordinates initial and ongoing training to the study team regarding protocol specificities, Case Report Form (CRF) completion, dashboards, Sponsor Standard Operating Procedures (SOPs), clinical plans and guidelines, data plans and timelines for the study. • Oversees resourcing allocations for CRAs and Central Monitors, site assignments and study team members' conduct, and identifies risks to delivery or quality. • Ensures quality of the clinical monitoring, central monitoring and site management deliverables within a project and maintain proper visibility of its progress by the use of approved systems and / or tracking tools. • Reviews the project oversight dashboards and other clinical trial systems (e.g. Clinical Trial Management System (CTMS), Electronic Data Capture (EDC), eDiary, Electronic Patient Reported Outcomes (ePROs),Trial Master File (TMF), IVRS/IWRS, Central Monitoring dashboards), to oversee site and patient activities, study team conduct and to ensure the data has been updated to reflect timely execution of all operational aspects (required visits/calls, duration, and frequency) according to plan. • Understands the monitoring strategy required for the study and, where required, participates in the development of the study risk assessment plan. • Is accountable for their assigned clinical team members' understanding, ongoing compliance and delivery according to the stated monitoring strategy, CMP/SMP, and risk plans. • Reviews the content and quality of site and central monitoring documentation (site monitoring calls, site visit reports, site letters, central monitoring reports and pertinent correspondence), to ensure they represent site management activities and conduct and that they appropriately convey any risks to protocol/GCP compliance, trial conduct, patient safety or data integrity. • Document requested revisions and approvals in CTMS. • Ensures these deliverables are provided according to company and/or sponsor specifications, including delivery deadlines. • Interacts with the client and other functional departments related to clinical monitoring, central monitoring and site management activities and deliverables. • Provides status updates on the clinical deliverables and risks to clients, project management and leadership as per departmental or study agreements. • Provides solutions for obstacles in protocol execution and site management. • Demonstrates understanding of other functions' roles in achieving compliance and delivery according to protocol, SOPs, ICH GCP and country regulations. • This may include data management, study start up, patient recruitment, medical monitoring, pharmacovigilance and Quality Assurance (QA). • Supports Inspection Readiness for clinical trial management scope. • Oversees CRAs and Central Monitors assigned to the study and routinely assesses study-specific process and training compliance, CMP compliance, and identifies emerging risks. • May develop and support execution of corrective action plans at site and study level. • Supports and completes activities to achieve data cut and lock deadlines. • Provides feedback to line managers on staff performance including strengths as well as areas for development. • May be assigned to larger,more complex trials.