Associate Director, Clinical Development Scientist

Job Title: Associate Director, Clinical Development Scientist Location: Boston, MA   At AstraZeneca, we pride ourselves on crafting a collaborative culture that champions knowledge-sharing, ambitious thinking and innovation – ultimately providing employees with the opportunity to work across teams, functions and even the globe.    Recognizing the importance of individualized flexibility, our ways of working allow employees to balance personal and work commitments while ensuring we continue to create a strong culture of collaboration and teamwork by engaging face-to-face in our offices 3 days a week . Our head office is purposely designed with collaboration in mind, providing space where teams can come together to strategize, brainstorm and connect on key projects.      Introduction to Role: The Associate Director, Clinical Development Scientist (CDS) may lead a cross functional team in the design and execution of a clinical study and may provide input into the  global clinical development plans and strategy for a therapeutic area. The job holder supports assigned clinical development physician(s) and the therapeutic area head with deliverables necessary for effective and efficient clinical development plan design and execution and therapeutic area strategy.      Accountabilities:   • Lead a team in preparation of clinical study related documents including protocols, charters, statistical summary reports, meeting presentations, publications, and clinical sections of regulatory documents (may manage several studies in parallel).  • Lead a study team to design a clinical protocol, including engaging with relevant internal and external partners; responsible for preparing materials and protocol defense presentation for C-PRC review. Represent the clinical study team at the clinical sub team.  • May supervise and develop clinical development scientists and/or fellows; Lead a team in preparation of clinical study related documents including protocols, charters, statistical summary reports, meeting presentations, publications, and clinical sections of regulatory documents   • Participate in Investigator meeting planning and execution and/or on-site initiation meetings  • Lead the execution of clinical trials; Monitor, clean, analyze and review safety and efficacy data to establish the presence or absence of trends and follow up as appropriate.  • Lead a team in study execution, including country and site selection, site training and start-up and data monitoring; expertise in data analysis and presentation required. Depending upon specific expertise in translational science, may lead a translational sub team of the clinical team.  • Liaise with other functions to build external expert consultations,  contribute to the development of study concepts and designs, protocols and study essential documents. • Engage with clinical investigators on clinical studies to enable quality clinical execution, analyze and interpret clinical data, and collaborate with the broader team to define clinical and therapeutic area strategy. • Engage with investigators, site staff, CROs, and site monitors to maintain passion and support enrollment for ongoing clinical studies. Where appropriate, serve as the SME for identification, translation, inclusion, implementation and reporting related to liquid, tissutal and/or imaging endpoints.  • Lead the execution of clinical trials and associated data collection activities, providing guidance to the clinical study team related to: country and site feasibility assessments and selection  • Site training and oversight  • Patient recruitment  • Ongoing data monitoring  • Study closeout  • Maintain awareness of internal and external developments (scientific, clinical, competitive, and regulatory) that could