.**Description****JOB SUMMARY**:**Responsible for managing and coordinating Early Phase Biometrics deliverables in projects ranging from standalone clinical pharmacology and biometrics to full service contracts.**:**JOB RESPONSIBILITIES**:- In collaboration with the clinical Project Manager (PM), manages Early Phase Biometrics activities for multiple projects in parallel, varying in size and complexity, with mínimal interaction from supervisor.- Lead and oversee interdisciplinary project teams to ensure Early Phase Biometrics delivery per agreed timelines and budget. Facilitate team building and communication.- Manages the financial aspects of assigned projects/programs related to assigned deliverables as needed. Ensures customers are notified of out of scope/change of scope items and invoiced in a timely manner.- Acts as a liaison and facilitator between Early Phase Biometrics and other departments within the company for project related tasks and/or issues.- May act as the primary liaison between CP department and the Customer to ensure project launch, conduct, and closeout according to contractual agreements.- Monitors and evaluates project progress through timelines and other tracking/analysis tools and metrics.- Set priorities and schedule activities of departmental resources, implement company objectives, and create alternative solutions to address business and operational challenges.- Produces and distributes status, resourcing and tracking reports to appropriate team members and senior management.- Develops contingency planning and risk mitigation strategies to ensure successful delivery.- May support proposal development through review of proposal text and pricing.- Contributes to developing project management processes within the Early Phase Biometrics department and in the Early Phase organization.- Contributes to improving processes to achieve greater efficiencies.**Qualifications****QUALIFICATION REQUIREMENTS**- BA/BS in life sciences, health care or related field- Moderate relevant clinical research experience with an understanding of clinical drug development and clinical trials operations- Excellent knowledge of clinical data management, biostatistics and medical writing processes- Project Management qualification i.E. Prince II or PMP / equivalent an advantage- Excellent communication, presentation, interpersonal skills, both written and spoken, with an ability to inform, influence, convince, and persuade- Good organizational, planning and time management skills with the ability to multitask under tight deadlines- Ability to be flexible and adapt to change, to work independently, as well as part of a multi-disciplinary team- Ability to make effective decisions and manage multiple priorities in a highly dynamic environment**Disclaimer**:Tasks, duties, and responsibilities as listed in this job description are not exhaustive