Senior Regulatory Start-Up Specialist

A leading clinical research organization in Melbourne is seeking a Senior Regulatory Start Up Associate. This role involves planning and reviewing regulatory submissions, providing guidance on local regulations, and ensuring compliance with timelines. The ideal candidate will have a graduate degree in a relevant field and 3-5 years of experience in a CRO or...

Precision for Medicine is a Clinical Research Organization that enables the science of precision medicine through novel clinical trial designs, operational and medical expertise, advanced biomarker and data analytics solutions, and a deep passion for rare diseases and oncology. In addition, we work across other therapeutic areas. Regulatory and Start Up...

Precision for Medicine is a Clinical Research Organization that enables the science of precision medicine through novel clinical trial designs, operational and medical expertise, advanced biomarker and data analytics solutions, and a deep passion for rare diseases and oncology. In addition, we work across other therapeutic areas. Regulatory and Start Up...

Senior Regulatory Start Up Associate - Australia The Senior Regulatory Start Up Associate is primarily responsible for planning, preparation, and review of country and site‑level ethics and regulatory authority applications and submissions during project start‑up, in compliance with ICH‑GCP and local regulatory requirements, to ensure timely clinical...

Senior Regulatory Start Up Associate - Australia The Senior Regulatory Start Up Associate is primarily responsible for planning, preparation, review of country and site level ethics and regulatory authority applications and submissions during project start-up, in compliance with ICH-GCP and local regulatory requirements, to ensure timely clinical trial...

Regulatory Submissions (Study Start-up) Manager Join to apply for the Regulatory Submissions (Study Start-up) Manager role at Medpace Regulatory Submissions (Study Start-up) Manager Join to apply for the Regulatory Submissions (Study Start-up) Manager role at Medpace We are currently seeking a full-time, office-based* Study Start Up Submissions Manager to...

Precision for Medicine is a Clinical Research Organization. Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry‑leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology, in...

A global clinical research firm is seeking a Country Approval Specialist in Sydney, Australia. Key Responsibilities Manage regulatory submissions and ensure site activation. Qualifications Strong attention to detail and 1+ years of experience in start‑up operations. This role offers comprehensive health benefits, flexible working arrangements, and...

Precision for Medicine is a Clinical Research Organization. Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology, in...

A leading clinical research organization in Townsville City is seeking a Regulatory and Start Up Specialist. This role involves preparing clinical trial application forms, communicating with authorities, and maintaining project plans. The ideal candidate should have a Bachelor's degree in life sciences, strong communication skills, and at least 1 year of...