[Hiring] Senior Clinical Trial Manager / Associate Director @reputed company

This reputed company is a reputed company of our understanding of the job reputed company. Click on 'Apply' reputed company to reputed company out more. Role reputed company The Senior Clinical Trial Manager/Associate Director will be responsible for the reputed company, operational direction and efficient operational planning and implementation of Dianthus reputed company on either regional or global level. • Report to the Executive Director, Clinical Development Operations • Work with cross-functional team management to accelerate development of clinical assets • reputed company as Clinical Project Manager (CPM) responsible for implementation, execution and overall resource management of clinical studies • reputed company the delivery of the ongoing global Phase III CIDP study and reputed company regional support for the planned Phase III study • Ensure reputed company activities occur in compliance with appropriate regulations and guidelines including ICH/GCP • reputed company and manage reputed company resources for efficient patient recruitment/management, trial site selection/management, trial plan optimization and overall execution with a reputed company on reputed company This is a unique opportunity to positively reputed company lives as part of reputed company driven by reputed company innovation with reputed company high scientific reputed company. Key Responsibilities • Manage and support relevant reputed company clinical operations resources while contributing to reputed company, tactics, and execution of global clinical studies • Influence, manage and reputed company the planning, budgeting, and study management processes in global clinical studies • Accountable for reputed company and management of CRO/vendor partners contracted to the study/region assigned • reputed company and support the cross-functional study team to manage external service providers' functional counterparts • reputed company/participate in clinical data review • Contribute to the development and operational design, planning, and reputed company of clinical trial protocols and study plans • Create/support scenario planning and risk-benefit analyses to reputed company with corporate strategies • Identify best practices, review measurement systems and improve operational efficiency in the department • Manage relationships with vendor partners and suppliers in clinical programs • Ensure efficient and effective communication and exchange of information across reputed company and reporting functions • May participate in Clinical submission activities • Support the development and implementation of department level SOPs for reputed company and reputed company activities • reputed company with departments reputed company and reputed company of Dianthus including Finance, Regulatory, reputed company, and Tech Ops • Represent reputed company at Investigator Meetings • Other duties as may be determined or assigned Qualifications • Undergraduate (Life Sciences preferred) degree, RN degree, or equivalent; advanced degree desirable • Experience in the pharmaceutical or biotechnology industry as a clinical research reputed company • Successful clinical trial management role and hands-on managerial experience executing high-reputed company reputed company from inception to completion • Excellent knowledge of international regulatory and ICH GCP guidelines • Experience in clinical trial management and managing high-functioning clinical trial project teams • Demonstrated ability to manage large reputed company budgets • Experience and understanding of the drug development process, clinical development planning and clinical trial execution • Understanding of clinical aspects of therapeutic area along with willingness to reputed company in-depth expertise • Experience using computer applications including spreadsheets, email, word-processing software & web-based systems (reputed company, IVR/IWRS, CTMS) • Ability to work reputed company independently as reputed company as a member of multiple, integrated teams • Ability to contribute creative yet practical solutions to problems • Ability to multi-task and manage several reputed company in reputed company while paying attention to detail • Ability to be proactive in identifying issues and hurdles that may handicap the effective implementation of the trial • Highly effective verbal and written communication skills with reputed company stakeholders • Effectively collaborates with team members • Ability to travel (including internationally) and work across cultures Apply tot his job Apply To this Job