Project Support Coord

hace 4 semanas

Xico, México Ppd A tiempo completo

Coordinates, oversees and completes functions on assigned trials activities detailed on the task matrix.- Performs department, Internal, Country and Investigator file reviews as assigned and documents findings in appropriate system.- Ensures allocated tasks are performed on time, within budget and to a high quality standard.Escalates in cases of variances (overburn/underburn).- Supports the maintenance of study specific documentation and systems including, but not limited to: study team lists, tracking of project specific training requirements, system access management, and tracking of project level activity plans in appropriate system.- Provides system (i.e. CTMS, Oracle Activate & eTMF) support by managing the access requests, tracking study level documents and maintaining audit readiness.- Performs administrative tasks on assigned trials including, but not limited to: timely processing of documents sent to CRG's/Client eTMF as required, performing CRG's/Client eTMF reviews, performing mass mailings and communications as needed, providing documents and reports to internal team members.- Supports scheduling and organization of client and/or internal meetings with completion and distribution of related meeting minutes.- Exports and prepares study metrics reports.- Maintains vendor trackers.- Assists with coordination and compilation of Investigator Site File (ISF) template and pharmacy binder, with instruction from the Clinical Team Manager.- When required attends Kick off and Project Launch meetings and takes notes, supports initial study set-up.- Ability to work in a team or independently as required- Good organizational skills and strong attention to detail, with proven ability to handle multiple tasks efficiently and effectively- Demonstrated ability to effectively analyze project-specific data/systems to ensure accuracy and efficiency- Strong customer focus- Good time management skills.Flexibility to reprioritize workload to meet changing project timelines- Demonstrated ability to attain and maintain a good working knowledge of applicable Country Regulations (if required), ICH Good Clinical Practices, and organization/Client SOPs and WPDs for all non-clinical/clinical aspects of project implementation, execution and closeout- Good English language and grammar skills and proficient local language skills (if required).Effectiveoral and written communication skills- Good computer skills, proficient in MS Office (Word, Excel, and PowerPoint) and ability to obtain knowledge and learn the required clinical trial systems- Ability to successfully complete CRG training program- Self-motivated, positive attitude and good interpersonal skills

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