Clinical Research Program Manager
Caris Life Sciences, Ltd.
Clinical Research Program Manager page is loaded## Clinical Research Program Managerlocations: Phoenix - CC17time type: Full timeposted on: Posted Todaytime left to apply: End Date: June 30, 2026 (30+ days left to apply)job requisition id: JR104694**At Caris, we understand that cancer is an ugly word—a word no one wants to hear, but one that connects us all. That’s why we’re not just transforming cancer care—we’re changing lives.** We introduced precision medicine to the world and built an industry around the idea that every patient deserves answers as unique as their DNA. Backed by cutting-edge molecular science and AI, we ask ourselves every day: That question drives everything we do. But our mission doesn’t stop with cancer. We're pushing the frontiers of medicine and leading a revolution in healthcare—driven by innovation, compassion, and purpose. **Join us in our mission to improve the human condition across multiple diseases. If you're passionate about meaningful work and want to be part of something bigger than yourself, Caris is where your impact begins.****Position Summary**Clinical Research Program Managers play a critical role within the Caris Operations business unit. Tasked with a diverse range of responsibilities supporting both internal and external customers as it relates to conducting clinical research, trial enrollment services and systems integrations with Caris. This role is hyper focused on downstream coordination and pull-through activities ensuring business requirements are met, responded to appropriately and delivering on time results. This role acts as a liaison between/across multiple departments within Caris, between Caris and the Precision Oncology Alliance (POA), and other business partners. The incumbent operates in a supportive function within the fast-paced multifaceted business unit supporting an array of business owners, relationships and initiatives.**Job Responsibilities*** Leads support activities related to conducting clinical research studies, clinical trial enrollment and POA research initiatives.* Ensures POA coverage teams are equipped with the necessary information to respond timely to site requests or address specific topics that fall within the purview of Caris Operations.* Conduct site facing presentations introducing study opportunities, data sharing and honest broker procedures/workflows, regulatory requirements, clinical trial matching and enrollment services, and system integrations (research and testing).* Development and deployment of a strategy to meet or exceed company's recruitment targets for investigative sites that will participate in Caris-sponsored research studies.* Responsible for project plans to onboard study sites who participating in Caris sponsored studies.* Responsible for navigating institutional policies and procedures within each site to create mutually agreed upon plan to execute a given project or initiative. Drives associated contracting processes, regulatory review and system access procedures/requirements.* Responsible for overall project plans, project management and successful implementation of study/initiative at assigned study sites.* Maintains proper visibility on all projects for which assigned sites are participating; proactively communicates status across all internal and external stakeholders.* Actively participates in contract review process and ensures regulatory documentation requirements are met.* Applies effective project management principles to ensuring all projects, initiatives, and contract deliverables are well documented, tracked and reportable.* Responsible for routine internal status reporting; communicating overall project, engagement status, issues, risk mitigation, and success factors.* Able to effectively manage multiple assignments/projects at simultaneously in a fast-paced and fluid environment.* Accepts other duties as assigned.**Required Qualifications*** Bachelor's degree* Strong business aptitude, customer focused mindset* Ability to work independently, self-starter, critical thinker and able to make decision.* Ability to effectively prioritize and manage multiple projects simultaneously; works well under pressure and able to meet tight deadlines.* Function in a fast-paced environment by adapting to changes while meeting critical deadlines.* Detail oriented and highly organized.* Strong communicator, both written and verbal* Projects a professional disposition, excellent work ethic and positive attitude.* Teamwork - Commitment to the successful achievement of team and organizational goals through a desire to participate with and help other members of the team.* Proficient in Microsoft Office Suite, specifically Word, Excel, Outlook, and general working knowledge of Internet for business use.**Preferred Qualifications*** Master's degree, in related field.* 5+ years' experience in a clinical research setting.* 2+ years of project management experience.* 2+ years relationship management experience**Physical Demands*** Will work at a computer a majority of the time as well as need to keep inventory and ordering records requiring the use of copiers, fax machines, and PDF scanners.**Training*** All job specific, safety, and compliance training are assigned based on the job functions associated with this employee.**Other*** Occasional business travel is required. Must live within 2 hours of a major airport.* Travel and work schedule may be required after hours. Responsibilities may include client meetings/dinners after normal business hours. Weekend/evening/holiday work may be required depending on business need, however, is not to be the norm.**Conditions of Employment:** Individual must successfully complete pre-employment process, which includes criminal background check, drug screening, credit check ( applicable for certain positions) and reference verification.This job description reflects management’s assignment of essential functions. Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time. Caris Life Sciences is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, gender, gender identity, sexual orientation, age, status as a protected veteran, among other things, or status as a qualified individual with disability. #J-18808-Ljbffr Caris Life Sciences, Ltd.
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- ...Clinical Research Program Manager page is loaded## Clinical Research Program Managerlocations: Phoenix - CC17time type: Full timeposted on: Posted Todaytime left to apply: End Date: June 30, 2026 (30+ days left to apply)job requisition id: JR104694**At Caris, we understand...SuggestedContract workWork at officeAfternoon shift
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..., or other staff involved in research protocol(s). Gives direction... ...therapeutic greater than minimal risk) clinical research protocols with... ...to assess feasibility and management of research protocols. Ensures... .../college Diploma/Certificate Program with at least 3 years of...Full timeInternshipFlexible hours- ...Fri, Days, 8am-5pm Category: Research Posting #: 1017137 Employee Type... ...of one or more clinical studies, typically requiring... ...study budgets and works with management to determine financial feasibility... ...of professional development programs to ensure understanding of most...Full timeWork at officeShift work
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...retirement package to secure your future. Responsibilities The Program Manager will oversee the Research Center or Program which serves as the research administrative base for several multicenter clinical trial/research groups with national/international participation....Permanent employmentFull timeWork at officeMonday to FridayFlexible hours- Dignity Health is seeking a Program Manager Revenue Integrity in Phoenix, Arizona, to oversee research patient billing processes, ensuring compliance with regulations and optimizing revenue cycle functions. The ideal candidate will manage a team, develop policies, and...
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- ...and Friendswood! Learn more at Castle Biosciences Inc. is growing, and we are looking to hire a full-time Clinical Research, Clinical Safety Manager working from our Phoenix, AZ, Friendswood, TX or Pittsburgh, PA office location, with a start date of August 1,...Full timeH1bWork at officeVisa sponsorshipWork visaMonday to FridayNight shift
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