A dual facing position; this person with take on full accountability for delivering elevated shareholder value through the design, implementation and execution of CDPs for both in-house and partnered projects.
The company has validated a world-first, synthetic and fully biodegradable technology for precision delivery of gene therapies. This position would suit a highly ambitious person seeking the opportunity to drive in-house and partner projects towards IND-enabling assets and into the clinic and beyond. You will be taking full advantage and reaping the industry-changing benefits of the company’s globally protected safe, targeted, effective gene therapy drug delivery technology.
This is a future-business critical opportunity, supported directly by the founding scientist and highly accomplished CEO.
- Extensive and successful background in CDP design, implementation and execution, including regulatory navigation with EMA, FDA and MHRA
- Extensive experience in clinical trial oversight
- Developed understanding of drug delivery for ATMPs
- Ability to travel globally as the role demands
As an SME Biotech, this role requires a highly ambitious spirit that thrives in a fully autonomous and hands on environment. You will be driven by the thrill of the entire process of clinical strategy, design and execution as well as clinical operation oversight and hold a deep passion to fulfill a mission to have a significant, global, industry-changing impact on the application of gene therapy delivery.
Due to the nature of this company and position, and as expected, there is already a high level of interest from candidates in Next Phase’s immediate network, so if this is something that has aroused great interest, and you believe you are a suitable consideration for this position, please contact firstname.lastname@example.org for more information urgently.
Best of luck!