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Job #02999

About our client Our client is a biopharmaceutical company that discovers, develops and commercializes therapeutic medicines for the treatment of serious medical conditions. The company has marketed products, an experienced management team and an empowering corporate culture that is focused on the professional development of its employees. This is a great opportunity for the right candidate! Position Location Clinical Program Manager Tarrytown, New York Salary Highly competitive package, commensurate with experience Responsibilities 1) Communicate operational needs effectively to ensure goals are met 2) Remain informed of all decisions to ensure established goals are attainable prior to the consensus to implement 3) Develop work plans, establish clinical research objectives, assign tasks and supervise Clinical Trial managers 4) Maintain schedules (timelines) for overseeing assigned clinical research studies and facilitate decision making in order to adhere to timelines 5) Provide guidance to Clinical Team by establishing clinical research goals that are aligned with established policies and standards for the department and organization 6) Identify and recommend changes to established practices and policies which affect subordinate resources 7) Direct the activities of resources, both internal and outside contractors/vendors with similar technical or functional duties 8) Recommend additional resources based on the need to meet goals and milestones 9) Answer questions from sites and document interactions and obtain updates 10) Coordinate supplies and manage drug issues 11) Collect regulatory documents 12) Interact with Data Management to ensure that data collected is accurate and data queries are resolved in a timely manner 13) Work with Data Management to ensure statistical analysis plan is developed and data is transferred to the company (as needed) 14) Interact with CRAs and Project Manager to ensure sites are being monitored appropriately, data is collected in a timely manner and study is progressing properly 15) Oversee internal aspects of trials 16) Ensure appropriate paperwork to Regulatory Department, adequate drug supply and coordination of sample shipments to Sample Analysis Department 17) Determine services to be provided to external laboratory, equipment and service vendors as well as ensure those services are provided according to the study needs and within budget 18) Deliver high quality program deliverables on time and within budget 19) Manage, track and troubleshoot a series of related trials within a single program 20) Identify program risks 21) Create and implement mitigation strategies proactively Requirements 1) Bachelor’s degree in Life Sciences (advanced degree preferred) 2) Minimum 7 years of clinical research experience in the pharmaceutical industry (multiple phases preferred) 3) Minimum 2 years of management experience 4) Experience in study start up, data lock and study enrollment 5) Background in oncology and ophthalmology 6) Willingness to work in an external environment (physician’s offices and hospitals) where exposure to pathogens is greater than internal environment 7) Willingness to travel – up to 25% (air, rail and automobile)