$200K — $250K *
To be successful, you will have previously will be responsible for building and maintaining effective CRO relationships that support the execution of clinical and non-clinical ADME/PK work. In this capacity you will be responsible for agreeing projects of work and negotiating costs and setting the outsourced DMPK budgets. You will also be able to interpret the returning data, provide presentations to the team and leadership on the data’s impact and be able to write summaries for key regulatory documents. This role reports the head of Clinical Pharmacology and Bioanalytical Sciences. At this stage the role will be an individual contributor, needing to work with matrixed functions, though future growth by the company may result in the opportunity to oversee direct reports.
How do you know if you’re the right fit?
If you are a highly self-motivated, driven individual who enjoys the challenges and opportunities available in a growing and transforming organization, this will be an opportunity for you to apply yourself, learn and deliver. You’ll thrive in an environment where you are involved in both the strategy (the bigger picture) and in the execution, and value proactive collaboration and teamwork to be successful. Additionally, your input will be expected to span the needs for both discovery and development and the opportunity to engage and learn about the other aspects of the broader Clinical Pharmacology discipline will be available.
Your experience will span along the range of the following responsibilities:
The other stuff
This is typically a role best suited for (Msc with 12 years of experience or Ph.D with 9 years of experience) who possess at least (8) years’ pharmaceutical/biotechnology experience (or other).
Valid through: 11/24/2020