Heather Ewing

· Ability to understand and follow company SOPs

· Review and assess protocol (including amendments) for clarity, logistical feasibility, safety, inconsistencies, etc when requested too.

· Assist PI and the SS to ensure that all training and study requirements are met prior to trial conduct

· Discuss study test products, required procedures, eligibility criteria, and impact on office flow with Investigator and site staff

· Assist with planning and creation of appropriate recruitment materials

· Assist in the development of recruitment plan and obtain a listing of potential candidates to contact from the subject database

· Actively work with the recruitment team in calling and recruiting subjects for your studies and other site studies

· Attend Investigator meetings.

· Coordinate and attend pre-study site visits, site initiation visits and monitor visits with clinical staff and Sponsor/CRO representatives and report summary to the Regional Manager if they are not in attendance

· Assist in the creation or review of sponsor-provided protocol specific source documents

· Determine facility, equipment and outsource vendor requirements and availability

· Ensure adequate supplies have arrived on site for protocol initiation

· Ensure

· Ability to understand and follow company SOPs

· Review and assess protocol (including amendments) for clarity, logistical feasibility, safety, inconsistencies, etc when requested too.

· Assist PI and the SS to ensure that all training and study requirements are met prior to trial conduct

· Discuss study test products, required procedures, eligibility criteria, and impact on office flow with Investigator and site staff

· Assist with planning and creation of appropriate recruitment materials

· Assist in the development of recruitment plan and obtain a listing of potential candidates to contact from the subject database

· Actively work with the recruitment team in calling and recruiting subjects for your studies and other site studies

· Attend Investigator meetings.

· Coordinate and attend pre-study site visits, site initiation visits and monitor visits with clinical staff and Sponsor/CRO representatives and report summary to the Regional Manager if they are not in attendance

· Assist in the creation or review of sponsor-provided protocol specific source documents

· Determine facility, equipment and outsource vendor requirements and availability

· Ensure adequate supplies have arrived on site for protocol initiation

· Ensure education of Assistant CTAs and other site staff, and/or sub-investigators is completed for required tasks. Ensure all training records for team members is up to date. education of Assistant CTAs and other site staff, and/or sub-investigators is completed for required tasks. Ensure all training records for team members is up to date.