Site Activation Specialist
1 month ago
We are currently looking for a Site Activation Specialist on a 6 month fixed term contract . Immediate Start
In this role, you will serve as the Single Point of Contact (SPOC) in assigned studies, acting as the main liaison between investigative sites, Site Activation Manager (SAM), Project Management team, managing and executing start up and site activation activities, plus amendment activities at a country level. All locations across ANZ considered.
Job Overview:
Your responsibilities will include performing start-up and site activation activities in accordance with applicable regulations, Standard Operating Procedures (SOPs), and work instructions. You will provide local expertise to SAMs and the project team during the initial and ongoing project timeline planning phases. Additionally, you will be responsible for preparing and reviewing ethics and regulatory documentation, ensuring their completeness and accuracy. Monitoring and tracking the progress, approval, and execution of various documents such as questionnaires, regulatory submissions, ethics approvals, Informed Consent Forms (ICFs), and Investigator Pack (IP) release documents will be a crucial part of your role.
You will also review, prepare, and negotiate study budgets and contracts with sites, while ensuring accurate maintenance of internal systems, databases, and tracking tools with project-specific information. Conducting quality control of documents provided by sites, obtaining the necessary documentation and approvals, and handling maintenance activities such as site budget and contract amendments will be among your key responsibilities.
Lastly, you will review site performance metrics and provide feedback to management based on your observations and analysis.
Qualifications:
Bachelor’s Degree in Life Sciences or equivalent work experience 1- 2 years’ experience 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 skills, ability to negotiate and problem solve. Good interpersonal and organisational skills Ability to work on multiple projects balancing competing priorities Willingness to learn and embrace emerging technology Knowledge and ability to apply ICH GCP and applicable regulatory guidelinesIf this sounds like you, please hit the APPLY button and the Talent Acquisition Team is looking forward to speaking with you
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at
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