Regulatory Submissions Associate — Clinical Trials

IQVIA is seeking a Clinical Trial Regulatory Manager in Bloemfontein, South Africa. The role involves preparing and reviewing regulatory documents for clinical trial submissions, providing guidance on straightforward and complex projects, and maintaining compliance with regulatory requirements. The ideal candidate will hold a Bachelor’s Degree in Lifescience and have 1-2 years of experience related to EU CTIS and global core packs. Strong communication skills and proficiency in software such as…