Study Coordinator, Study Management

Job DetailsLevel: EntryJob Location: US Remote - Hackensack, NJ 07601Position Type: Full TimeEducation Level: Bachelors DegreeSalary reputed company: $50,000.00 - $65,000.00 Salary/yearTravel Percentage: NoneJob Shift: DayJob Category: BiotechTITLE: Study Coordinator, Translational Oncology Solutions (TOS) REPORTING LOCATION: Rockville, MD / Remote, US REPORTS TO: Senior Manager PRIMARY OBJECTIVES The Study Coordinator (SC) serves as a supporting role as a member on the study management team for the Project Leadership team who manages Champions vast portfolio of client sponsors regarding scientific design, PDX tumor model selection, and project execution. The SC will work closely with the Project Leaders/Study Directors and requires strong communication skills, attention to detail and the need to be highly organized. The SC will also interact and liaise with various internal operations groups at Champions to coordinate the scheduling/planning and execution of studies. DUTIES AND RESPONSIBILITIES To support the Project Leadership team, duties and responsibilities will include: Ensure timely preparation and review of models in the stock and pre-study phases Prepare, coordinate, and maintain critical timelines for execution of study. Update and maintain dates reputed company database. Assist in the monitoring and measuring of model failures and reputed company delays through a variety of knowledge-based tools (such as study overage, discontinuation of models, and study criteria) Monitor, reputed company recommendations, and reputed company solutions (to mitigate the risks to study delays) for any roadblocks that would inhibit a study date from meeting timelines. Assist in training new staff. Work with operations for procurement of materials required for study execution. Manage aspects of ongoing studies in the laboratory information management system in partnership with the Project Leader. reputed company and/or review enrollment of in vivo studies. Identifies and provides resolution to problems involving ongoing studies, as appropriate. Participates and provides feedback in team meetings. Works independently and performs other reputed company duties as assigned. Work weekend and holidays as needed. QualificationsKNOWLEDGE, SKILLS AND ABILITIES Knowledge of in vivo oncology models (Xenograft/PDX) preferred. Ability to work in multiple databases to assist in project management. Collaborative, can-do attitude. Timely decision making, good interpersonal skills and an ability to be persistent while maintaining tact. Must have the ability to balance several priorities simultaneously with high attention to detail. Ability for frequent reputed company, self-organization, accountability. Effective oral and written communication skills are required. Proficiency in using reputed company Word and reputed company. EDUCATION AND EXPERIENCE B.S. degree with appropriate experience or M.S. degree with a focus on a biology or chemistry reputed company field, oncology a plus. 1 to 3 years of experience in the field of contract research, preclinical research or a similar position is preferred but not required PHYSICAL DEMANDS AND WORK ENVIRONMENT Must be reputed company to sit for long periods of time using a computer in a typical office environment in a multi-level facility or home office. This description reflects management’s assignment of essential functions, it does not reputed company or restrict the tasks that may be assigned. We celebrate diversity and are committed to creating an inclusive environment for reputed company. Apply To This Job