Senior Regulatory Submissions Specialist

Regulatory Submissions (Study Start-up) ManagerJoin to apply for the Regulatory Submissions (Study Start-up) Manager role at MedpaceRegulatory Submissions (Study Start-up) ManagerJoin to apply for the Regulatory Submissions (Study Start-up) Manager role at MedpaceWe are currently seeking a full-time, office-based* Study Start Up Submissions Manager to join...

Regulatory Submissions (Study Start-up) ManagerJoin to apply for the Regulatory Submissions (Study Start-up) Manager role at MedpaceRegulatory Submissions (Study Start-up) ManagerJoin to apply for the Regulatory Submissions (Study Start-up) Manager role at MedpaceWe are currently seeking a full-time, office-based* Study Start Up Submissions Manager to join...

OverviewWe are currently seeking a full-time, office based Study Start up Submissions Coordinator Entry to join our Clinical Operations team in the Australia, Melbourne office. This role is a vital part of the team to accomplish tasks and projects that are instrumental to the company's success. If you are interested in an exciting career where you can use...

OverviewWe are currently seeking a full-time, office based Study Start up Submissions Coordinator Entry to join our Clinical Operations team in the Australia, Melbourne office. This role is a vital part of the team to accomplish tasks and projects that are instrumental to the company's success. If you are interested in an exciting career where you can use...

Regulatory Specialist RoleThis is a challenging opportunity for a skilled Regulatory Specialist to join our team and support the development, preparation, and submission of regulatory applications for prescription medicines and other therapeutic goods across Australia and New Zealand.The successful candidate will play a key role in delivering high-quality...

Global Regulatory Submissions ManagerWe are seeking a seasoned professional to oversee the entire lifecycle of global regulatory submissions. The ideal candidate will have extensive experience in clinical research, preferably with a Contract Research Organization (CRO), and exceptional communication skills.Main Responsibilities:Manage all aspects of global...

About the RoleThe Regulatory Affairs Specialist plays a pivotal role in ensuring compliance with local regulatory requirements.Prepare, review, and submit regulatory submissions for new product registrations and lifecycle maintenance variations to TGA and Medsafe.Ensure compliance with TGA and Medsafe regulatory frameworks.To achieve this, you will be...

Job Title:Regulatory Submissions Specialist, About the JobWe are seeking a skilled Regulatory Submissions Specialist to join our Clinical Operations team in Melbourne, Australia. As a key member of our team, you will play a vital role in ensuring the success of our clinical trials by preparing and submitting regulatory documents to authorities.Your primary...

About This OpportunityThe role of Associate Director, Regulatory Affairs will play a key part in driving projects forward for the Regulatory Affairs team within the ANZ affiliate.Key Responsibilities:Strategic Leadership: Contribute to the development of the RA organization's vision and direction at a country level.Regulatory Compliance: Ensure that...

Job Title: Senior Compliance AdvisorAbout the Role:This senior role plays a crucial part in shaping our compliance strategy by offering expert guidance and leadership on both regulatory and internal compliance issues.You will be a reliable partner to business units managing energy markets operations, ensuring that compliance requirements are well understood,...