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Study Start Up Specialist

5 months ago

Toronto, Canada Alimentiv Full time

**Job Title**: Study Start-Up Specialist

**Job Location**:Toronto, ON

**Job Salary**: $50,000 - $84,000

**Job Reports to**: Project Director

**Department/Unit Name**: Full Service-Clinical Project Management

**Job Summary**:
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.

**Areas of Responsibility**:

- 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**:
**Working Conditions**:
Home Based
- Accommodations for job applicants with disabilities are available upon request.