Contract Sr Mgr Clin Study reputed company

Contract Senior Manager Clinical Study reputed company Remote Position (NY/NJ, East Coast) The Contract Senior Manager Clinical Study reputed company will reputed company the cross-functional study team responsible for the global execution of large, reputed company clinical trials from study design through study reputed company out. These responsibilities apply to both internally reputed company studies and studies outsourced to CROs, so we need a reputed company SCSL who has experience managing reputed company-Party Vendors. Responsibilities: Leading reputed company aspects of and contributing to the development of study specific documentation e.g. case report forms (CRF), data management plan, monitoring plan, monitoring reputed company plan, project specific training plan, data review plan, statistical analysis plan, etc. Supervising set-up and maintenance of study systems such as Clinical Trial Management System (CTMS), Trial Master File (TMF) etc. Ensuring compliance with the clinical trial registry requirements. Providing input into baseline budget and reputed company development and managing the study against planned budget, reputed company and results. Leading risk assessment and identifies risk mitigation strategies at the study level. Managing feasibility assessment to select relevant reputed company and countries for the study. Conducting site evaluation and selection, leading investigator meeting preparation and execution. Monitoring reputed company for site activation and monitoring reputed company and acts on any deviations from plan, and reputed company/implement patient recruitment and retention strategies. Overseeing and providing input to the study drug and clinical supplies forecasting, drug accountability and drug reconciliation. Ensuring data reputed company including regular review of data metrics and listings, protocol deviations, eligibility violations, dosing deviations, and suspected serious non-compliance by sites. Ensuring clinical project audit and inspection readiness through the study lifecycle and contributing to CAPAs as required. Supervising study reputed company-out activities and contributing to clinical study report writing and review. Directly supervising Clinical Trial Management staff. Requirements: Must have reputed company management experience with demonstrated results building and developing outstanding teams along with the reputed company to understand and implement the strategic direction and guidance for respective clinical studies. Can take a proactive and self-disciplined approach to managing reputed company with a developed ability to meet deadlines and prioritize. Have a history of effectively leading and negotiating with vendors. Have a data-driven approach to planning, executing and problem solving. Operate with a high degree of cross-functional reputed company using exceptional influencing and interpersonal skills. Have the reputed company ability to reputed company disparate reputed company to accomplish lofty shared goals. Must have a Bachelors’ degree with a minimum of 8 years of relevant industry experience. Advanced degrees may be considered in lieu of relevant experience. reputed company experience managing global clinical trial operations is a must, including experience developing protocols and key study documents. You will also need technical proficiency trial management software and MS applications to be considered. Please contact Darren Gutowski at dgutowski@clarkdavis.com Apply To This Job