Support Project Management, Regulatory, and Contract and Legal in all site-related start-up activities. Establish relationships with study personnel at sites and act as main Alimentiv contact during site start-up. Prepare, distribute and follow-up on start-up documents with sites. Plan and track site start up activities and data using designated systems and tools. Provide reports on intelligence and metrics related to study start-up activities.
*Please note there is 1 position cross-posted in several locations, although we are open to considering candidates from the following countries: Poland, UK, Romania, Germany
Site Start-Up Packages
In cooperation with Project Management create study-specific start-up document package.
Distribute and follow up with sites to obtain the required executed documents.
Review content and correctness of returned documents from the sites, in accordance with internal standards.
In conjunction with Regulatory Affairs, ensure that the correct and complete packages are obtained within the planned timelines.
Site Contract and Budget Negotiation
In co-operation with Contract and Legal, obtain feedback on suggested site and investigator contract language.
Act as main point of contact for sites to obtain feedback on budget and contract negotiations.
In conjunction with the Project Manager, provide sites with the suggested study budget and negotiate within pre-approved margins.
Site Intelligence Tracking
Maintain site intelligence tracker with data related to specific requirements for study sites such as start-up timelines, budget, contract negotiation timelines and prerequisites, patient recruitment data, etc.
Provide input for suggested site list during start-up using past experiences with potential study sites.
Site Start-Up Planning and Tracking & Project Management support
Act as main contact for study sites during start-up.
Develop and maintain relationships with study sites that will facilitate timely completion of start-up.
In conjunction with project management and CRAs, plan start-up actions and provide expected SIV dates for individual sites based on previous start-up metrics, as well as regulatory and /RB timelines.
Track progress of start-up activities in smart sheet and/or CTMS.
Maintain up to date knowledge, ensure adherence and compliance with local regulatory requirements and associated documentations.
Provide support to project management with study related activities as required.
Qualifications
Applicants should have a minimum of one to three years of related work experience with ongoing training, or a minimum of a one-year College Advance Diploma/Degree in a relevant field of study, preferable in Health or Life Sciences, or Clinical Research. The successful candidate must exhibit the following skills: Excellent communication skills. Knowledge of start-up requirements for clinical sites. Experience in working directly with clinical study sites through previous involvement in studies. Very high sense of urgency.
Working Conditions
Home-based
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*Accommodations for job applicants with disabilities are available upon request.
