• Providing leadership and support as it pertains to the operation of toxicology, ADME-PK, and bioanalysis • QCs on non-clinical study (GLP or non-GLP) protocols and reports, and study record and study material management constitute a great portion of this role • Track study milestones and deliverables for internal reporting and management • Serve as a primary liaison among nonclinical team, legal and finance to facilitate contract placement and execution promptly • Track invoices and ensure timely payment in coordination with the finance group • Support budget tracking and forecasting for all relevant studies • Assist with literature research, and regulatory and submission readiness support as needed • Other Duties: Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.

• Serve as the primary escalation point for clinical operations issues and assist with real-time problem solving to maintain workflow continuity. • Support daily operations by monitoring worklists, turnaround times, and support queues to ensure timely case processing and resolution. • Provide task-based guidance and direction to team members to support workflow efficiency and consistency. • Assist with staff coordination, including schedule adjustments and coverage planning, in partnership with the Manager. • Provide advanced radiologist and site support, including resolving image and order discrepancies, assisting with dictation system issues, and supporting urgent communications. • Act as a liaison between radiologists, sites, IT, and internal teams to facilitate communication and resolve operational or technical concerns. • Troubleshoot system and workflow issues, escalate to IT or Level 2 support as needed, and monitor tickets through resolution. • Support onboarding and ongoing training by reinforcing workflows and best practices. • Assist the Clinical Support Services Manager with investigating site concerns, delays, and workflow challenges, escalating as appropriate. • Participate in Manager-on-Duty (MOD) coverage as needed. • Perform other duties as assigned.

Role Description As a per diem Staff Pharmacist you’ll play a vital role in delivering safe, accurate, and efficient pharmacy services. This is a hands-on opportunity to make a direct impact by ensuring the accuracy of medication orders, verifying technician-prepared products, and safeguarding controlled substances. You’ll contribute to a high-performing team by: - Mentoring new staff - Maintaining seamless daily operations - Supporting the Director in optimizing pharmacy performance Pharmacy Location: Located within Cumberland Hall Hospital, 270 Walton Way, Hopkinsville, KY 42240 Hours of Operation: Monday - Friday from 7:30am to 4pm as needed - weekend on call (typically remote) If you are located in Louisville, KY, you will have the flexibility to work remotely* as you take on some tough challenges. Primary Responsibilities: - Fill in for Pharmacist during PTO or sick time - Oversee Pharmacy Technicians Qualifications - ACPE-accredited pharmacy degree (PharmD preferred) - KY state pharmacist license in good standing - 1+ years of recent pharmacist experience (hospital setting preferred) - Skilled with pharmacy systems and Microsoft Office Requirements - All employees working remotely will be required to adhere to UnitedHealth Group’s Telecommuter Policy Benefits - Comprehensive benefits package - Incentive and recognition programs - Equity stock purchase - 401k contribution (all benefits are subject to eligibility requirements) The hourly pay for this role will range from $44.09 to $78.70 per hour based on full-time employment. We comply with all minimum wage laws as applicable.

• Serve as a key member of the global strategy team, presenting compelling strategies that strengthen commercial efforts and drive growth. • Collaborates closely with commercial and operational teams by delivering site analytics, feasibility intelligence, capability assessments, and country specific or multi‑specific or multi‑center strategy considerations. • Conducts fair market value (FMV) reviews for proposals involving external site partners by leveraging an Excel-based costing tool to generate accurate FMV reference budgets. • Generates standardized core budget templates using the Excel-based costing tool and GrantPlan to provide project teams with consistent, data driven baseline budgets that support effective site negotiations-driven baseline budgets that support effective site negotiations. • Develops evidence based, data driven clinical trial strategies informed by expert insights and rigorous analytics. • Deliver these strategies through white papers, executive summaries, proposals, bid defenses, feasibility assessments, competitive landscape analyses, and client facing presentations. • Leverages data mining and research to identify trends in trial environments—such as country/site distribution, competition, and historical performance—to support strategic recommendations. • Maintains and enhances the global external site partnership network and applicable Strategy & Planning Study Resourcing databases • Assist in overall department goals and daily operations process efficiencies which may require the development of SOPs, job aids, work instructions, templates, checklists, trackers and forms, including controlled documents. • The development of clinical trial strategies requires the development and management of external clinical investigator site partner relationships globally, requiring close collaboration across administrative, operational, and medical staff at external clinical sites. • Develop and build relationships with key investigation partners which may require governance, site success initiatives, site capability visits, site specific performance, issue escalation and resolution. • Perform additional tasks as delegated by department manager