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Job Location | Cambridge |
Education | Not Mentioned |
Salary | Competitive salary |
Industry | Not Mentioned |
Functional Area | Not Mentioned |
Job Type | Permanent, full-time |
Clinical Research Scientist/Senior Clinical Research Scientist – Late RIA Are you a highly motivated, interactive and creative Scientist ready to work in a matrix environment to advance Clinical Drug Development programs If you can envision providing scientific expertise in a role that can impact patients’ lives – join us today!Our overall research ambition within Respiratory, Inflammation and Autoimmune (RIA) for the future is to transform the lives of patients through our growing portfolio of inhaled combinations at the core of care, biologics for the unmet needs of specific patient populations, and scientific advancements in disease modification with the ambition of achieving remission or even cures for patients.In this role, you will provide scientific and clinical input to all aspects of late stage product development. This includes design, delivery and interpretation of pivotal clinical trials, mechanistic studies, studies that further characterize the overall benefit, risk value of RIA Therapeutic Area (TA) products and in late stage development and other indications.Main Duties and ResponsibilitiesThe objectives of the Clinical Research Scientist/ Senior Clinical research Scientist will be set by the Group Director in agreement with Global Clinical Lead(s). Your role will have a special focus on late stage clinical trials within RIA, where you will work in close collaboration with the study team physician with all aspects of scientific input, clinical data quality metrics and safety evaluation.You will be encouraged to collaborate with colleagues in the RIA development and early development groups. To be successful in your role, you will seek input from the appropriate functional experts and coordinate these activities in support of clinical studies and programs.Furthermore, you will ensure that the safety evaluation process is seamless and complete and independently lead specific activities and contribute to science story preparation, regulatory submissions, process improvement and mentoring other scientists.We will rely on you to: