Senior role within the Study Startup team
Work with a team of global experts within the Sponsor
Flexible working arrangements- no travel involved
About the company
A leading pharmaceutical company that develops depression, endocrinology, oncology, and cardiovascular care medicines.
About the opportunity
The Senior Feasibility Associate is accountable to ensure the investigator sites meet the requirements to enrol study participants into clinical trials and support ongoing activities during site maintenance and closeout.
Initiate Investigator site activities, including collection and submission of regulatory documents,customisation and negotiation of informed consent documents, serve as the point of contact for a site's ERB and Competent Authority, communicate, negotiate budgets with site personnel and internal teams, negotiate and obtain fully-executed contract, track and ensure site compliance to required training, and effectvely drive timelines aligned with company priorities.
Communicate with sites to enable startup and maintain active collaboration with sites during maintenance and close-out
Identify, communicateand resolve issues
Manage investigator payments and any other financial transactions related to Trial Capabilities which includes but not limited to vendor creation and management, PO creation and maintenance, payment activities, country/site budget tracking and payment related issue resolution.
Ensure country specific and data provacy requirements are incorporated into submission documents and any other documents/systems.
Skills and Experience
Minimum 2 years local study startup experience
Bachelor's degree preferably in a scientific or health related field
Understanding of the overall clinical development paradigm and the importance of efficient site activation
How to Apply
Click apply or contact Christine Bristol,Division Manager on +61 2 8877 8766 for a confidential discussion.
( SK924529A )
4 days ago
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