Professional development lead

Title: Drug Development & RWE Lead At Inovia Bio we believe that drug development is in dire need of disruptive thinking. incumbents that extract as much value as possible from drug developers and their companies while often delivering utter garbage. From the way data is used to make early decisions through to how development plans can be accelerated and de-risked, there are significant opportunities to get drugs to patients faster. Your role will be central to our mission of revolutionising drug development. Inovia Bio is a Tech Bio Startup based in London. The clinical development & RWE lead at Inovia operates differently – We believe that drug development can only be solved by the merging of medicine and technology…and so will you! Internal product development: “You’re tired of the manual, repetitive and expensive model of drug development” You will partner with engineering to provide expertise and input on the development of novel tools that have significant impact on the drug development process. You will be hands on with vast multimodal data and generate your own ideas of what else we should be building. You’re passionate about drug development and see opportunities and pathways where others don’t” You will work closely with Inovia’s partners to support their drug development programs. You’re excited to get your hands dirty and can look at data through a novel lens” You’ll look at data through unique perspective and identify opportunities. Everyone in the medical team at Inovia codes – So do you! You will be proficient with SQL + either R or Python. You’re able to run complex analysis and are comfortable figuring out new approaches. You have expertise in the medical sciences and can think about diseases from the ground up. You will have a degree in the medical sciences. You have the ability to understand a condition by examining its biological, physiological, and pathological foundations. You understand why four different pharmaceutical companies developing the same drugs are likely to have vastly different outcomes. You are an expert in clinical trial designs   and clinical development strategy. You have experience working with secondary data and large RWE datasets. You’ve written Protocols, SAPs, TFLs and CSRs. You have a deep understanding of the current pharmaceutical development landscape. You have a deep understanding of regulatory requirements and the current opportunities in drug development. Your response to “can you develop this external control arm study” is hold my beer. You’re excited to work with engineering, medical and commercial teams to develop products or new ideas. In God we trust- all others must bring data. You are profoundly data driven and believe that the right data trumps experience any day of the week. We’re a fast-paced venture backed startup that are making outsized impacts for our partners, will you join us on our journey? Competitive salary. Private Health Insurance. Hybrid work environment. Rapid progression opportunities. Zero political work culture.