3 Jobs found

BioArctic is a pioneering Swedish biopharma company dedicated to developing innovative treatments for neurodegenerative diseases. We are now seeking a Director Business Development to strengthen our organisation and support the expansion of our pipeline.You will play an important role in identifying and evaluating opportunities for partnerships and collaborations, as well as supporting commercial evaluation of project ideas. You will report to our Senior Director of Business Development. Main Responsibilities     Identify and evaluate external licensing and partnership opportunities     Lead the commercial evaluation of internal & external project ideas     Build and maintain long-term relationships with potential partners worldwide     Work closely with colleagues across functions and wit...

We do nothing regular within regulatory! Are you an experienced regulatory expert looking for a role where you can truly make an impact? At RegSmart you will help drug development companies navigate complex regulatory challenges in both the EU and US, from early development to clinical trials and beyond. As Senior Advisor you will provide high-level strategic advice as well as hands-on regulatory support. You will work across a variety of projects, often taking the lead, and collaborate closely with colleagues, clients and authorities. The role combines independence with teamwork in a dynamic, growing company. Depending on your expertise and client needs, you may: • Develop regulatory strategies in pre-clinical and clinical phases, main focus is projects in early stages • Identify data gap...

We do nothing regular within regulatory! Have you worked with CMC to secure pharmaceutical quality in the development of biologics? At RegSmart you will use your expertise to guide companies developing biologics and ATMP through complex regulatory challenges.As Senior Advisor you will support clients with both strategy and hands-on work. You will manage multiple projects, sometimes in a leading role, working closely with experienced colleagues while enjoying a high degree of independence.Depending on your expertise and client needs, you may:     Drive regulatory CMC development plans for biologics and ATMP     Prepare and review regulatory documentation     Lead and participate in scientific advice meetings     Interpret guidelines, or find new solutions when none exist     Manage and coor...