Senior Medical Director, Clinical Development
Senior Medical Director, Clinical Development
This is what you will do:
As a Senior Medical Director, Clinical Development 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 / profile
Lead 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 submissions
Initiate and support key contacts with opinion leaders, and help develop alliances as appropriate
Write and check content and quality of product related publications and input to development of publication strategy
Follow important developments and trends in the clinical & scientific literature to provide value and direct strategy across Rare Disease Clinical Development
You will need to have:
Medical Degree with a subspeciality preferably in Internal Medicine, Paediatrics, Endocrinology or Oncology with many years in clinical practice.
You have several years of clinical drug development within a pharmaceutical company environment.
A good understanding of more than one development function
Phenomenal interpersonal skills
Excellent verbal and written communication skills in English
Ability to acquire and assimilate knowledge in different disciplines, diseases and therapeutic areas
Share our values to put patients first, follow the science, do the right thing and play to win
A curious and entrepreneurial mindset
If you are ready to make a difference - apply today, and we'll make it happen together!
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 authorisation and employment eligibility verification requirements.
