dossier

Informations générales Référence COR-ALTE-42943   Date de parution 28/08/2026 Localisation GRANVILLE...

Precision for Medicine Group seeks a Regulatory and Site Start Up Specialist in Australia. The role focuses on regulatory submissions, site activation, and managing essential documents to enable timely trial initiation.The candidate will prepare submission dossiers, coordinate with ethics committees, and support site contracts while ensuring compliance with...

Evolution Precast is seeking a meticulous Quality Administrator to join our Hunter Operations Quality team, coordinating quality documentation, records and reporting across multiple precast facilities in NSW.Reporting to the Quality Manager, you will maintain ITPs, NCRs and project handover packs, prepare quality dossiers and dashboards, and support internal...

Abbott Laboratories in Australia is seeking a Health Economics & Reimbursement Analyst to support reimbursement strategies and market access across Abbott Medical Australia’s portfolio. You will gather data, conduct HTA and budget analyses, and collaborate with cross-functional teams to ensure alignment with Australian requirements. The role involves MSAC...

Pharmako Biotechnologies is a leading Australian manufacturer of nutraceutical products and is seeking a Regulatory Affairs Associate to join the team in Sydney. The role supports regulatory, compliance and product development across medicines, foods, cosmetics and related products. Reporting to the Regulatory Affairs Manager, you will assist in submissions,...

Precision Medicine Group seeks a Regulatory and Site Start Up Specialist in Australia to manage regulatory submissions and site activation activities across assigned sites. You will prepare CTAs and dossiers for competent authorities and ethics committees, maintain essential documents, and collaborate with CRAs to ensure timely site activation. You will...

Johnson Controls in Brisbane seeks a seasoned Document Controller / Project Coordinator to support building technology projects. You will manage documentation, ensure compliance, and assist project teams from initiation to completion.Responsibilities include control of document registers, transmittals, and handover dossiers, plus coordinating reviews with...

Precision Medicine Group seeks a Regulatory and Site Start Up Specialist in Australia to manage regulatory submissions and site activation activities across assigned sites. You will prepare CTAs and dossiers for competent authorities and ethics committees, maintain essential documents, and collaborate with CRAs to ensure timely site activation. You will...

Precision Medicine Group seeks a Regulatory and Site Start Up Specialist in Australia to manage regulatory submissions and site activation activities across assigned sites. You will prepare CTAs and dossiers for competent authorities and ethics committees, maintain essential documents, and collaborate with CRAs to ensure timely site activation. You will...

Precision Medicine Group seeks a Regulatory and Site Start Up Specialist in Australia to manage regulatory submissions and site activation activities across assigned sites. You will prepare CTAs and dossiers for competent authorities and ethics committees, maintain essential documents, and collaborate with CRAs to ensure timely site activation. You will...

Precision Medicine Group seeks a Regulatory and Site Start Up Specialist in Australia to manage regulatory submissions and site activation activities across assigned sites. You will prepare CTAs and dossiers for competent authorities and ethics committees, maintain essential documents, and collaborate with CRAs to ensure timely site activation. You will...

Precision Medicine Group seeks a Regulatory and Site Start Up Specialist in Australia to manage regulatory submissions and site activation activities across assigned sites. You will prepare CTAs and dossiers for competent authorities and ethics committees, maintain essential documents, and collaborate with CRAs to ensure timely site activation. You will...

Precision Medicine Group seeks a Regulatory and Site Start Up Specialist in Australia to manage regulatory submissions and site activation activities across assigned sites. You will prepare CTAs and dossiers for competent authorities and ethics committees, maintain essential documents, and collaborate with CRAs to ensure timely site activation. You will...

Abbott Laboratories in Australia is seeking a Health Economics & Reimbursement Analyst to support reimbursement strategies and market access across Abbott Medical Australia’s portfolio. You will gather data, conduct HTA and budget analyses, and collaborate with cross-functional teams to ensure alignment with Australian requirements.The role involves MSAC...

Precision for Medicine is seeking a Regulatory and Site Start Up Specialist to lead regulatory submissions and site activation across assigned countries. You will manage CA/EC dossiers, IRB interactions, and essential document review, while partnering with sites and internal teams. The ideal candidate has a life sciences degree with 1+ year in...

Precision for Medicine is seeking a Regulatory and Site Start Up Specialist to lead regulatory submissions and site activation across assigned countries. You will manage CA/EC dossiers, IRB interactions, and essential document review, while partnering with sites and internal teams. The ideal candidate has a life sciences degree with 1+ year in...

Precision for Medicine is seeking a Regulatory and Site Start Up Specialist to lead regulatory submissions and site activation across assigned countries. You will manage CA/EC dossiers, IRB interactions, and essential document review, while partnering with sites and internal teams. The ideal candidate has a life sciences degree with 1+ year in...

Precision for Medicine is seeking a Regulatory and Site Start Up Specialist to lead regulatory submissions and site activation across assigned countries. You will manage CA/EC dossiers, IRB interactions, and essential document review, while partnering with sites and internal teams. The ideal candidate has a life sciences degree with 1+ year in...

Precision for Medicine is seeking a Regulatory and Site Start Up Specialist to lead regulatory submissions and site activation across assigned countries. You will manage CA/EC dossiers, IRB interactions, and essential document review, while partnering with sites and internal teams. The ideal candidate has a life sciences degree with 1+ year in...

Precision for Medicine is seeking a Regulatory and Site Start Up Specialist to lead regulatory submissions and site activation across assigned countries. You will manage CA/EC dossiers, IRB interactions, and essential document review, while partnering with sites and internal teams. The ideal candidate has a life sciences degree with 1+ year in...