Clinical Science Program Specialist (100% Remote)

Clinical Science Program Specialist (100% Remote) Tucson, United States | Posted on 06/23/2026 Our client, a worldleader in diagnostics and life sciences, is looking for a “ClinicalScience Program Specialist (100% Remote)". Job Duration:LongTerm Contract(Possibility Of Extension) Pay Rate : $35/hr on W2 Company Benefits: Medical, Dental,Vision, Paid Sick leave, 401K Coordinate and managemultiple clinical testing and laboratory services projects from initiationthrough completion, serving as the primary point of contact for pharmaceuticalclients. Drive cross-functional project execution, oversee sample workflow activities,and ensure timely, accurate delivery of clinical study results in a regulatedenvironment. Key Responsibilities: Managemultiple clinical testing and lab services projects under the guidance ofthe Program Manager. Developproject plans, timelines, and coordinate cross-functional activities toensure on-time execution. Monitorproject progress, identify risks and bottlenecks, and implement solutionsto maintain milestones. Overseesample processing workflows and ensure accurate reporting of results. Serveas the primary liaison for pharmaceutical clients, CROs, siteinvestigators, and internal stakeholders. Coordinatemeetings, prepare agendas, document minutes, and communicate projectupdates. Trackand maintain project reports and clinical study data. Promotebest practices and continuous improvement across clinical operations. Qualifications: Bachelor’sdegree required; Life Sciences preferred. 2+years of project coordination, clinical trial coordination, or projectmanagement experience in the CRO, diagnostics, pharmaceutical, orregulated industry. Exposureto clinical studies and regulated documentation. Strongorganizational, communication, and collaboration skills. Abilityto manage multiple projects in a fast-paced environment. PreferredQualifications: Experiencewith companion diagnostics (CDx), clinical testing, or biosamplemanagement. Knowledgeof clinical trial management processes and PMI methodologies. Experiencewithin the diagnostics or pharmaceutical industry. If interested, pleasesend us your updated resume at #J-18808-Ljbffr Dawar Consulting