Sr. Study Start-Up Specialist
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Job Location:
Monthly Salary:
Posted on:
30+ days ago
Vacancies:
1 Vacancy
Job Summary
Lead the site identification to site activation on Full Service and/or Medical R&D Clinical Trials in collaboration with the Sponsor Project Management Monitoring and Site Management Regulatory Affairs and Contracts and Legal. Develop and utilize intelligence databases and tools to identify the best fit sites for a study. Establish relationships with study personnel at sites and act as the main Alimenitv contact during site start-up. Prepare distribute and follow-up on start-up documents with sites. Plan and track site start up activities using designated systems and tools present overview to Sponsor and Study team during review meetings. Identify and initiate best practices reports on intelligence and metrics related to study start-up activities.
Site Start-Up Planning and Tracking & Project Management Support
- Primary contact and lead for study site start-up
- Oversee Startup Specialist/s that may additionally support the study
- Provide guidance tools and best practices to support Project Management to drive faster study startup including the creation of the overall study critical path timelines
- Develop and maintain relationships with study team and sites to facilitate timely completion of start-up activities.
- Proactively plan priorities with the collection of site essential documents based on regulatory submissions and approvals
- Track progress of startup activities and provide status reports on an ongoing basis
Site Feasibility
- Contribute to the country and site selection strategy for a study by utilizing intelligence databases and tools to identify the best fit sites for a study
- Contact and collect feasibility data from sites working closely with contracts and legal to ensure CDAs are in place if required and provide information to Project Management and Monitoring and Site Management
- Ensure that sites move through the feasibility process promptly tracking each step and identifying risks to start-up timelines potentials barriers and escalate to the project manager
- Contribute to the identification and initial feasibility of new sites
Site Start-Up Packages
- In cooperation with Project Management and Regulatory Affairs 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.
- Support Regulatory and sites with local EC site submission packages tracking of document versions and approvals when required
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 create and provide sites with the suggested study budget and negotiate within pre-approved margins.
- Contribute to the development of the site contracting and site budget intelligence databases
Site Readiness
- Ensure essential document package for IP release is complete and signed working closely with Project Management Regulatory Affairs and Contracts & Legal
- Oversee the tracking of pre-site activation activities working with Project Management CIMS Monitoring and Site Management to ensure expedited site activation.
Contributions to the development of the Study Startup Team
- Contribute and maintain the study startup intelligence databases
- Identify process improvements updates to quality and guidance documents
- Contribute to new innovations introduced to improve and expedite the site startup process
- Providing guidance/mentorship/support to more junior members of the team
Qualifications
- Undergraduate degree (Bachelors or Honours Bachelors) with minimum 46 years of relevant experience
- Bilingual in French/English strongly preferred
$78000 - $130000 a year
bonus
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Required Experience:
Senior IC
Key Skills
- Sales Experience
- Crane
- Customer Service
- Communication skills
- Heavy Equipment Operation
- Microsoft Word
- Case Management
- OSHA
- Team Management
- Catheterization
- Microsoft Outlook Calendar
- EHS
About Company
Accelerate your GI clinical trials with Alimentiv’s site network, clinical trial services, medical imaging, and biomarker discovery
