Senior Regulatory Affairs Specialist

Shorla Oncology develops innovative solutions into effective oncology treatments to improve patients’ lives. The patients’ needs are at the heart of our innovation, ensuring we deliver affordable, accessible medicines and provide a significant clinical impact.

Shorla Oncology has core values of compassion, commitment, innovation, tenacity and collaboration. At Shorla Oncology we feel passionately about the work that we do and the patients that inspire us. Our focus on oncology gives us the opportunity to truly impact lives.

We are seeking a Senior Regulatory Affairs Specialist to join our US team, working directly with our Regulatory Affairs Manager and other senior level team members. This position will play a pivotal role in our organisation through product development, submission and approval, post approval and lifecycle management, and other strategic activities.

The successful candidate will have at least 5 years work experience in a regulatory role within the pharmaceutical industry in the United States and a third level degree in a science discipline. The Senior Regulatory Affairs Specialist will have in depth knowledge of US FDA guidelines and directives associated with the regulation of pharmaceutical products. The successful candidate will enjoy a competitive salary and benefits package in a flexible working environment and will be keen to work and develop in a fast paced environment in a scaling company.

Please send your resume to: