(Senior) Medical Director, Clinical Development Sciences Reports to: Executive Director, Clinical Development • RDM
Location: Barcelona,
This is what you will do: As a (Senior) Medical Director, Clinical Development Sciences you will be a key component of the Project Team, working synergistically with the global project team lead and clinical team as the expert in medical scientific aspects of the drug and its development during clinical phase. The nature of this role may require working across projects and diseases.
The key accountabilities will include driving components of or the whole clinical programme strategy for individual projects, as well as the overall concept and design of clinical trials within Alexion, Clinical Development Team. You will also be the scientific leader with regards to the development, interpretation and implementation of new endpoints.
For Alexion, we work across multiple rare diseases in specialities focused on Endocrinology, Neurology, Hematology, Cardiology, Nephrology, Pediatrics and Oncology. We are now looking for a new colleague in the growing disease area covering rare endocrinology, metabolic bone disease and rare oncology.
You will be familiar or become familiar with relevant Regulatory guidelines for drug development for the key Endocrinology and rare bone diseases, as well as current treatment guidelines, relevant competitor trial designs and data as these are continually evolving. As such this will enable you to build novel and innovative approaches cross all phases of Clinical development, including Experimental Medicine studies generating data for Go/NoGo decision making to Phase 3 registrational studies
Additional tasks may include the set-up, design, conduct, reporting and regulatory submission of clinical trials; participation and leadership of cross-functional workstreams within and outside of Alexion. Finally, as a Medical Director you will play a crucial role in leading cross-project activities to direct Rare disease Clinical Development Strategy.
You will be responsible for: Guide clinical science aspects of the Clinical Development Plans (CDP) and Clinical Study Protocols in keeping with the approved CDP and ensuring linkage of trial data to target product claims / profileLead clinical scientific input to the set-up, design (target population, translational biomarker selection and low reference value/target value characterization for decision making), study analysis planning and reporting as well as regulatory submissionsInitiate and support key contacts with opinion leaders, and help develop alliances as appropriateWrite and check content and quality of product related publications and input to development of publication strategyFollow important developments and trends in the clinical & scientific literature to provide value and direct strategy across Rare Disease Clinical DevelopmentYou will need to have: We believe that you hold a Medical or Biomedical PhD or is a MD with a subspeciality preferably in Internal Medicine, Pediatrics, Endocrinology, or Oncology with many years in clinical practiceYou have several years of clinical drug development, medical affairs or medical research experience within a pharmaceutical company environment. You also possess a degree of specialist knowledge of the medical and scientific activities related to a particular therapeutic area, in this instance, preferably Endocrinology.We would prefer for you to have: A good understanding of more than one development functionPhenomenal interpersonal skillsExcellent verbal and written communication skills in EnglishAbility to acquire and assimilate knowledge in different disciplines, diseases and therapeutic areasShare our values to put patients first, follow the science, do the right thing and play to winA curious and entrepreneurial mindsetIf you are ready to make a difference - apply today, and we'll make it happen together!
We welcome your application no later than June 15, 2024 AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.
#J-18808-Ljbffr
