.Project SpecialistThis position is remote and can be based anywhere in Mexico.
Management and administration of projects at assigned pharmaceutical clients.
The projects will include clinical data quality services (e.G., EDC, ePRO, IxRS, rater training, endpoint reliability, scale management, cognition, etc.)
for said pharmaceutical clients.KEY ACCOUNTABILITIESData/Site Management- Manage identification and resolution of clinical trial data inquiries/data changes and communication to internal and external multi-function resources within project teams- Manage communications with client (e.G.
pharmaceutical sponsor, CRO) and site personnel regarding site/study details- Facilitate weekly data review meetings with clinical trial study team leaders- Own in-study/maintenance transactional project activities throughout entire project lifecycle, e.G.
project variable fees, inter-department workflow assignment, issue escalation- Prepare study materials, including system requirements, data transfer documentation, questionnaires, rater experience surveys, response sheets, and other documents as required- Set up master systems, additional study hardware, study site folders, and data folders for clinical trial execution- Coordinate and set-up data for system launch as assigned- Produce data reports (e.G., weekly, interim, final, etc.)
for submission to pharmaceutical clients- Facilitate the closedown and archival of system databasesTraining Event Management- Attend international large scale training events (e.G.
Investigator's Meetings, Phase I site staff training) and facilitate training sessions (requires frequent overnight domestic and international travel)- Coordinate with clients, vendors, and expert consultants to ensure all logistics, materials, and technologies necessary for successful training events are in place- Independently facilitate virtual training sessions (e.G