Clinical Science Program Specialist

We are seeking a Clinical Science Program Specialist to support clinical testing and laboratory services projects within a fast-paced pharmaceutical and diagnostic environment. This individual will serve as the primary point of contact for pharmaceutical clients while coordinating cross-functional teams to ensure successful execution of clinical studies and testing programs. Key Responsibilities Manage multiple clinical testing and laboratory services projects from initiation through completion under the guidance of a Program Manager. Serve as the primary contact for pharmaceutical clients and maintain strong customer relationships. Develop project plans and coordinate timelines across multiple functional teams. Track project milestones, identify risks, bottlenecks, and delays, and proactively drive resolutions. Oversee day-to-day sample processing workflows and ensure accurate reporting of clinical study results. Coordinate cross-functional activities to ensure project deliverables are completed on schedule. Collaborate with internal teams, Contract Research Organizations (CROs), site investigators, and external stakeholders. Lead project meetings, prepare agendas, document meeting minutes, and communicate action items. Track, maintain, and communicate project status reports and clinical study data to clients. Support continuous improvement initiatives and promote best practices across the clinical sciences team. Required Qualifications Minimum 2 years of experience in project coordination, clinical trial coordination, or project management within a regulated environment. Experience in the CRO, pharmaceutical, diagnostic, biotechnology, or clinical research industry. Exposure to clinical studies and regulated documentation. Experience managing projects with aggressive timelines and milestone-driven deliverables. Strong communication, organizational, and collaboration skills. Preferred Qualifications Knowledge of standard Project Management (PMI) methodologies. Experience with clinical trial management processes. Understanding of biospecimen/sample management and clinical testing workflows. Experience supporting companion diagnostics (CDx) or diagnostic development programs. Knowledge of pharmaceutical and diagnostic industry practices. What We’re Looking For A highly organized, client-focused professional who can manage multiple priorities, coordinate cross-functional teams, and successfully drive clinical projects from initiation to completion in a regulated environment. #J-18808-Ljbffr Pharmaceutical Company