Regulatory Affairs Specialist

Upsilon Global are seeking a freelance Regulatory and Start-Up Specialist / Contracts and Budget Specialist for an upcoming Oncology Phase I/II Breast Cancer Study .

Location : Spain
Study Duration : 6 months
FTE : 0.5
Responsibilities :
Oversee site activation, maintenance, and regulatory activities for assigned projects.
Manage and coordinate all necessary documentation for site initiation and regulatory submissions.
Ensure compliance with regulatory requirements and help facilitate the timely execution of clinical trial phases.
Provide strategic oversight for contracts and budgets related to the study.
Requirements :
Bachelor's degree in life sciences or a related field.
Proven experience in regulatory and start-up processes within clinical trials.
Strong understanding of oncology studies, particularly in Phase I settings, is highly preferred.
If you are an expert in clinical trial start-up and regulatory activities and have a passion for advancing oncology research, we would love to hear from you!

Interested experts can contact Juliana Madiba or call +44 203 875 9966 for more details.