• Responsible for the clinical operations of a project within a defined regional/global level. • Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and Investigator sites. • The COL acts as a primary liaison between the CRAs and the clinical project team. • Additional responsibilities include project specific training of CRAs, conducting assessment visits with CRAs. • Implementation of enrollment and recruitment strategies, preparation of the monitoring plan and other structural documentation. • Oversight of monitoring visit scheduling, site and monitoring performance metrics, issue escalation and corrective actions. • Develop study tools for site and CRA use, review visit reports, review and track protocol deviations. • Support other objectives for clinical operations and the clinical project team.

• Navigates various electronic health record (EHR) and computer applications to perform job duties to support patient care, care management initiatives, revenue cycle, Health Maintenance and regulatory requirements • Receives, sorts, prepares, and scans internal and external clinical documentation into the EHR according to Health Information Management (HIM) procedures • Analyzes non-interfaced patient laboratory reports to ensure patient identifiers and compliance with all applicable regulations • Utilizes optical character recognition software to electronically and or manually enter appropriate data into the EHR • Identifies, creates, or releases the appropriate laboratory tests by applying knowledge of medical terminology and laboratory nomenclature • Discretely abstracts and imports laboratory results and other clinical documentation into the EHR • Communicates with patient care and external performing laboratories via phone, email, fax, Epic In-Basket, and other methods to provide education, STAT laboratory data entry services and other required information

Role Description The Clinical Advisor position is an exciting opportunity for pharmacists to leverage their clinical expertise in a client-facing role. This role will support the management of a large custom client with commercial and EGWP business. You will utilize your clinical and analytical skills within a managed care environment to positively impact the health of plan members while also helping to reduce healthcare costs. - Serve as the clinical subject matter expert on the clinical account team. - Leverage your analytical skills to provide clinical consulting services through analyzing drug utilization patterns and trends for the client. - Work collaboratively with the client on commercial and Medicare Part D clinical initiatives and programs. - Act as a liaison with internal teams and other clinicians to support clinical programs on behalf of the client. - Maintain above-average client satisfaction scores. This position can be located anywhere in the United States, with the flexibility to work remotely or in a corporate hub location. You must be willing to travel up to 5-10% of the time. Qualifications - 3 years of managed care experience and/or 1 year of CVS Health or other Managed Care Residency program. - Active pharmacist license that is in good standing in state of residence. - Demonstrated proficiency in using Microsoft applications, especially Excel, PowerPoint, and Word. - Strong analytical skills and demonstrated comfort in working with large sets of data. - Excellent presentation and oral/written communication skills. - Demonstrated experience in Formulary and Utilization Management within PBM environment. - Commitment to client service and relationship building. - Knowledge of PBM adjudication engines and other systems leveraged in support of pharmacy benefit clients. - Ability to travel typically 5-10% of the time. Requirements - Experience supporting clinical pharmacy programs serving commercial and Medicare Part D/EGWP clients. - Advanced analytical skills with specific focus on quantitative analysis methods strongly preferred. - Established knowledge of supporting formulary and benefit setup and coding strongly preferred. - Expertise with PBM adjudication engines and other systems leveraged in support of pharmacy benefit clients. - Working knowledge of the different drug compendia adopted in PBM work. - Strong business acumen. - Experience in a client-facing role. - Ability to work on multiple projects, prioritize, and resolve complex problems. - Experience managing template and/or customized formularies and/or PBM clinical pharmacy programs. Education - Bachelor of Science, Pharmacy or PharmD. Benefits - Comprehensive benefits package designed to support the physical, emotional, and financial well-being of colleagues and their families. - Medical, dental, and vision coverage. - Paid time off. - Retirement savings options. - Wellness programs and other resources, based on eligibility. Pay Range The typical pay range for this role is: $110,925.00 - $249,600.00. This pay range represents the base hourly rate or base annual full-time salary for all positions in the job grade within which this position falls. The actual base salary offer will depend on a variety of factors including experience, education, geography, and other relevant factors.

Role Description We are seeking a Global Clinical Project Manager - Vendor Management Expert to join our Single Sponsor Department . In this role, you 'll become an expert in Vendor Management for global clinical trials across all phases (Phase I–IV), ensuring seamless execution from study start-up through close-out. Qualifications - Global Clinical Project Management experience - Strong Vendor Management expertise: - Central lab - eCOA - IRT - ECG - Imaging - Ancillaries - Patient Recruitment & Retention - Must have experience managing at least 2 of these vendors - Deep understanding of clinical operations processes and vendor service categories - Excellent project management skills to drive efficiency and collaboration - Strong communication and influencing abilities to partner effectively across functions - Proven ability to manage risk and performance issues in a fast-paced environment Requirements - Vendor Oversight & Coordination – Manage vendor activities across the study lifecycle, ensuring timely and high-quality deliverables - Study Start-Up Support – Oversee vendor deliverables during study initiation, ensuring smooth onboarding and activation - Risk & Performance Management – Track vendor performance, identify risks, and escalate issues as needed - Site Readiness & Activation – Drive vendor activities to support site activations and ensure study milestones are met - Study Close-Out – Coordinate vendor deliverables that support Database Lock and study closure Benefits - Vendor service excellence at the study level - Vendor onboarding and performance tracking - KPI (Key Performance Indicator) and KQI (Key Quality Indicator) dashboards to monitor vendor effectiveness - Site readiness monitoring and documentation - Risk mapping with contingency planning - Vendor cost control and oversight Company Description IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.