
Global Pharmaceutical Liaison
2 weeks ago
You will have the opportunity to work with a leading pharma & biotech company, helping them advance new drugs and devices.
- Support preparation of submission packages (IRB/ERC, regulatory agencies)
- Trail and site administration: tracking and updating study metrics
- Setup and maintain TMF/eTMF, documents collection and quality check
- Liaise with clinical sites, as well as internal and external stakeholders
- Coordination on drug supply planning, provision and destruction process, trial equipment and materials planning and management
- Vendor management: printing, translation and other vendors
- Distribution of site materials and equipment
- Meetings coordination
Key Requirements:
- Previous clinical trial experience in pharmaceutical or biotechnology industry or investigative site
- Bachelor's degree or equivalent preferred
- Australian study start-up processes knowledge
- Attention to detail, passion and reliability
- Excellent communication skills
- Familiarity with Essential Documents, CFR and GCP/ICH
- Proficiency in technological systems (Microsoft Office, TMF, CTMS)
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