
Clinical Study Activations Expert
7 days ago
We are seeking a skilled Site Activation Specialist to join our team.
Key Responsibilities:- Act as Single Point of Contact (SPOC) in assigned studies, liaising between investigative sites, Site Activation Manager (SAM), and Project Management team.
- Execute start-up and site activation activities in accordance with applicable regulations, Standard Operating Procedures (SOPs), and work instructions.
- Provide local expertise to SAMs and the project team during initial and ongoing project timeline planning phases.
- Review, prepare, and negotiate study budgets and contracts with sites.
- Monitor and track progress, approval, and execution of various documents, including ethics approvals, Informed Consent Forms (ICFs), and Investigator Pack (IP) release documents.
- Bachelor's Degree in Life Sciences or equivalent work experience.
- 0 - 2 years' experience in Clinical Research or Site Start-Up within a CRO/Pharmaceutical Company, ideally in Australia/New Zealand.
- Knowledge of clinical systems, procedures, and corporate standards.
- Good communication, negotiation, and problem-solving skills.
- Ability to work on multiple projects, balancing competing priorities.
- Willingness to learn and adapt to emerging technology.
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