• 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.

• 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. • 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. • 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. • 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. • 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 activities. • 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 IRB 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 documentation. • Provide support to project management with study related activities as required.

• Responsible for the application of biostatistical methods to support clinical trials and data management • Act as subject matter expert providing statistical support to project teams and stakeholders • Prepare statistical analysis plans and oversee project data collection and management • Collaborate with medical directors and technical writers on study reports and presentations

• Teach martial arts through the Karate Zoo enrichment program. • Use individual attention to ensure each child succeeds. • Ensure classes are fun and maintain a stress-free environment. • Utilize positive reinforcement to encourage children’s progress. • Follow the Karate Zoo Coaching Manual & Curriculum.