Job Description

Take your career to the next level and lead challenging study activation process in Australia. You will support clinical research teams and ensure PSI projects start smoothly and on time.

We're looking for a Study Startup Specialist II to join our team on an 18-month contract to support increased project demands. This newly created role is an excellent chance for someone looking to gain hands-on experience in clinical research or transition into a Study Startup position. To be considered, you must be based in Sydney and able to meet our current hybrid working arrangement.

You will:

- Maintains study-specific and corporate startup tracking systems
- Facilitates site budgets and contract negotiations
- Supports site regulatory document collection




- Under supervision, may prepare initial and amendment submission dossiers to competent authorities, ethics committees, and/or site submission dossiers (as applicable)
- Communicates with the project team and investigational sites throughout the entire duration of the study
- Develops site specific startup timelines and enrollment projections and is responsible for meeting the site activation milestones
- May review study specific translations
- Supervises Trial Master File (TMF) maintenance throughout the study startup phase

📌 Study Startup Specialist II (18-months contract) (Sydney)
🏢 Psi Cro
📍 Sydney