• Collaborate with Product Management to align vended solution and business need • Create value for customers and organization while mitigating risk • Validate hypotheses during product/feature discovery through continuous testing • Establish product/feature roadmap and goals with Product Management • Collaborate with internal and external contacts to analyze needs and align product roadmap to strategic goals • Create Release Plans and manage releases • Establish sprint goals in coordination with the team

• Accountable for oversight of all assigned studies within the country in accordance with the overall development plan and clinical operations plan and under the direction of the global team (Global Clinical Trial Manager), including adherence to quality, timelines and budget. • Accountable for planning and executing assigned country study goals and commitments, and as needed, leading, organizing, and participating in regional and/or local meetings and training sessions to implement country-level recruitment plans. • Develops, builds and maintains optimal relationships with key institutions within the country (i.e. Site Alliance Sites), working closely with the Medical Science Liaisons, Global Site Management and Central Services, and other departments as indicated according to the Site Engagement Strategy. • Drive the identification and inclusion of sites that have access to and can enroll patients who are from groups that have been historically underrepresented in clinical trials (per FDA Guidance for Industry for Improving Enrollment of Participants from Underrepresented Racial and Ethnic Populations in Clinical Trials). • Oversees regional study feasibility, site monitoring performance, quality metrics and all relevant activities for assigned studies. • Drives evidence-based site recommendations and selection. • Provides support and training for sites to support diverse recruitment and retention, review, assist and optimize site-level diversity plans as needed, check and challenge progress and coordinate and align central efforts across sponsor and CROs. • Align local and central initiatives and advise and guide on effective community engagement activities. • Conduct co-monitoring and site identification visits, as needed. • Collaborates cross-functionally to build and maintain strong relationships and interaction at the country local level (i.e. Medical Science Liaisons, Medical Monitors, Clinical Scientists, etc.) that directly contribute to key study activities and milestones. • Communicates regularly on country study (ies) status and escalates unresolved issues appropriately to the Regional Clinical Operations Head, North America, Clinical Operations Asset Lead, Clinical Operations Executive Therapeutic Head, and/or Global Study Team. • Collaborates with the Global Study Team, and when necessary, develops and executes the local implementation of the risk management plans, identifying critical issues for the country and ensuring contingencies are established and captured in the study level risk management plan. • For in-house studies, works with the Study Start-Up Team to ensure timely submission of all regulatory, IRB and administrative submissions and helps ensure their appropriate approval. • Collaborates in local quality/compliance reviews, internal audits, and regulatory inspections, ensuring inspection readiness at all times and implementation of Corrective Action Plan for assigned studies. • Ensures that clinical data from sites are of quality and delivered in accordance with established data entry and cleaning timelines and deliverables. • Represents country and line reports and provides the Global Study Team with actionable country-specific feedback. • Works closely with counterparts in the Regional Clinical Operations Organization to discuss and share country best practices, and contribute to process and initiatives that improve quality and effectiveness and that provide visibility to the Regional Clinical Operations organization. • Ensures that the Incyte Clinical Trial Management and various business intelligence and tracking systems are complete and up to date for assigned studies. • Proactively incorporate learning and recommendation from study debriefs, best practices and lessons learned. • Maintains oversight and ensures consistency across studies and alignment across CROs for outsourced studies. • Makes an active contribution to therapeutic area strategy teams (i.e. Global Study Team, Asset Lead Meetings, etc) ensuring knowledge sharing of regional interest. • Serves as an active contributor and rotating member on the Protocol Review Committee (PRC). • Manages issues related to local invoices and provide oversight of any budget reconciliation, in collaboration with Global Clinical Study Manager and relevant departments. • If appropriate, review CRO monitoring plans, training plans and relevant study plans for studies conducted in the region.

Role and Responsibilities The Clinical Pharmacist will help our communities thrive by optimizing medication management to allow our physicians more time to focus on patient care and support care coordination for assigned patient cohorts. The Clinical Pharmacist will work closely with the care coordination team and with physicians to ensure assigned patients are on intended prescribed therapies, understand their medication therapy and receive appropriate adherence coaching. Core Functions - The Clinical Pharmacist reports to the management staff. Daily tasks will also be directed by the pharmacy services team. - Provides telephonic follow up with members to provide medication reconciliation and medication management to assigned patients including transitional care and chronic disease support. - Complete assigned tasks related to medication management services. - Working with member, physician, health system(s), pharmacy services, and other care providers to meet the member’s individual needs based on protocols and referrals, - Coordinating transitional management including: - Obtaining medication orders - Complete medication reconciliation. - Work with Engage team to ensure medication provided until PCP follow-up. - The Clinical Pharmacist, Engage: - Provides medication management services utilizing prescribed workflows. - Complete assigned appointments in accordance with workflow. - Assess patient adherence behaviors. - Eliminate barriers to adherence. - Assess appropriateness of therapy provided by the pharmacy. - Document appropriately in Engage application and EnterpriseRx as applicable. - Work with central or local pharmacy to obtain and process prescriptions. - Communicate with providers regarding services provided. - Support the member education goals regarding their specific chronic condition based on the Plan of Care. - Support the evolution of pharmacy services delivery for key patient populations if applicable. - All communications will be conducted in a professional manner. - Remains objective and unbiased decisions in their medication management review and recommendations and not participate in any way in the delivery of care to the patient. - Administers tasks as detailed in the member specific Plan of Care. - Completes clear and concise documentation in Care Management programs. - Complies with Customer Service expectations as applicable to the Department and Health Plan. - Comply with all departmental policies and procedures. - Participate in departmental and company in-services as appropriate. - Recognizes and adheres to the scope / limitations of job requirements. - Performs other related duties as assigned. Qualifications and Education Requirements - PharmD - TX state pharmacy license and/or assigned market license. - Strong patient engagement skills including active listening, de-escalation intervention training and ability to teach complex topics in an understandable manner. - Strong organizational and time management skills, able to work with little supervision while handling numerous projects at once. - Excellent written/verbal communication skills, especially the ability to communicate telephonically in a professional and effective manner. - Computer literacy in Word, Excel. Location Plano, Texas (Remote) Department 5500 - Rx Engage Employment Type Full Time

Who We Are PathAI is on a mission to improve patient outcomes with AI-powered pathology. We are transforming traditional pathology methods into powerful, new technologies. These innovations in pathology can help accelerate drug development, improve confidence in the accuracy of diagnosis, and get life-saving therapies to patients more quickly. At PathAI, you'll work with a diverse and talented team of people, who are dedicated to solving complex problems and making a huge impact. Where You Fit PathAI is seeking a dynamic clinical project manager who will report to the Head of Clinical Operations to drive our clinical study roadmaps by partnering with internal and external stakeholders. Scientific and project management skills will be key to success in driving the necessary studies for pre- and post-market assessment of our products, as well as clinical trial services. What You’ll Do - Responsible for, and must have a demonstrated ability to successfully develop, implement, manage, and complete clinical trials operationally within designated programs and timelines. - Lead development and communication of presentations to keep internal and external teams aware of progress, timelines, and risks, ensuring successful completion of projects. - Generate high quality trial documentation, properly capturing trial activities and workflows, with high attention to detail. - Manage day to day monitoring of study activities and any issues that may arise. - Partner with cross functional internal teams (Engineering, Clinical Science, BioPharma Laboratory, etc.) and external stakeholders to manage, adjust, and revise project timelines/budgets as necessary. Must be able to resolve problems using FDA and other regulations, adherence to GCP requirements, and through regular site interactions. - Demonstrate excellent interpersonal skills, ability to bring teams together to successfully plan and execute PathAI clinical trials, and ability to prioritize with multiple competing priorities. - Manage external vendors, as needed. What You Bring - 3+ years of project management experience in medical device and/or drug development clinical trials and a BS or BA in a relevant scientific discipline, or 1-2+ years of experience with an M.S. or PhD in a relevant scientific discipline. - Robust understanding of clinical trial regulations, GCP and GCLP. - Experience in digital pathology, radiology or other imaging technology-based clinical trials is highly preferred. - Good organizational skills, attentive to details, and able to multitask. - Project Management Certification is a plus. - Strong understanding of laboratory practices, histology, and pathology preferred. - Experience in MASH, IBD, and Oncology preferred We Want To Hear From You At PathAI, we are looking for individuals who are team players, are willing to do the work no matter how big or small it may be, and who are passionate about everything they do. If this sounds like you, even if you may not match the job description to a tee, we encourage you to apply. You could be exactly what we're looking for. PathAI is an equal opportunity employer, dedicated to creating a workplace that is free of harassment and discrimination. We base our employment decisions on business needs, job requirements, and qualifications — that's all. We do not discriminate based on race, gender, religion, health, personal beliefs, age, family or parental status, or any other status. We don't tolerate any kind of discrimination or bias, and we are looking for teammates who feel the same way. The cash compensation outlined below includes base salary or hourly wage and on-target commission for employees in eligible roles. The summary below indicates if an employee in this position is eligible for annual bonus, overtime pay and equity awards. Individual compensation packages are tailored based on skills, experience, qualifications, and other job-related factors. Annual Pay Range: $69,750 - $106,950 Not Overtime Eligible Eligible for Equity #LI-Boston, MA or Remote