Regulatory Manager (Clinical Trials)

Precision for Medicine is not your typical CRO. At Precision for Medicine we have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost and success rate of bringing life-changing therapies to patients. What sets us apart is the way we integrate clinical trial execution with deep scientific knowledge, laboratory expertise and advanced data sciences. We have a strong focus on Oncology and Rare Disease. Precision for Medicine are recruiting for a Regulatory Manager (Clinical Trials) to join our team. As a key member of our regulatory department, you will be responsible for ensuring that all clinical trials conducted by Precision for Medicine are in compliance with relevant regulations and guidelines. This includes but is not limited to: - Developing and implementing regulatory strategies for clinical trials - Providing regulatory guidance and support to study teams - Coordinating and preparing submissions to regulatory authorities - Maintaining accurate and up-to-date records of all regulatory activities - Collaborating with internal stakeholders, including project managers, scientists and laboratory staff. The ideal candidate will have a strong understanding of clinical trial regulations and guidelines, particularly those related to Oncology and Rare Disease. You will also be expected to stay up-to-date with changes in regulations and guidelines, and to apply this knowledge to ensure compliance with all relevant regulatory requirements. In return for your hard work and dedication, we offer a competitive salary and benefits package, as well as opportunities for professional growth and development.