-
cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world. You will participate in pre-clinical drug discovery and development
-
of laboratory notebook records and adherence to safety policies is strictly required. QUALIFICATIONS PhD with a minimum of 2 years of post-doc experience. Experience in obesity-related physiology is required
-
to ensure operational excellence in the execution of the project's strategy. QUALIFICATIONS MD or MD/PhD (or equivalent degree(s)) with relevant postgraduate clinical training. Approximately 8-10 years
-
characterize and develop drug candidates from early phases of development to commercial launch. As a Director in the group you will lead a team of analytical scientists to assess the chemical and physical
-
cutting edge design and process development capabilities to accelerate and bring the best-in-class medicines to patients around the world. What You Will Achieve As an Associate Scientist, you will be
-
developing and maintaining quality programs, processes and procedures that ensure compliance with established standards and guidelines. In this role, you will manage and support the operational process and
-
cutting edge design and process development capabilities to accelerate and bring the best-in-class medicines to patients around the world. What You Will Achieve As a Senior Associate Scientist, you will be
-
. Participates in the planning, execution and data review for allocated studies. Works directly with clinical research personnel in reviewing data, performing physical assessments, medical histories, and