Vacancy has expired
|Job Ref:||15e470d1||Employer:||Direct Solutions - Canada||Country:||Canada||County/State:||Ontario||City:||Mississauga||Address:||Post Date:||23/10/2016 09:13|
General Responsibilities:Assist in the overall conduct of clinical studies for BE and Phase 1-4 studies including but not limited to:Recruitment, screening, and coordination of patient visits as per study protocolsExecution of all aspects of study visits as experience and training allowPerform clinical and study procedures as per study protocols, ensuring minimal deviations and proper tracking and reporting when deviations occurInteract with Principal Investigator, sponsor, manager and Scientific Director and other study coordinators to ensure all aspects of protocols and study requirements are understoodAssist in design, implementation and coordination of all aspects of data collection, source documentation and CRF transcription as per protocol, SOPs and ICH/GCP guidelinesParticipate in development and execution of Quality Control processesPrepare for and support QA audits and sponsor monitoring visitsStudy drug managementLab Sample processing, labelling, storage, shipment, documentation and record keepingSite Regulatory Documentation collection and managementParticipate in Environmental Chamber validations and maintenance; write validation protocols and reports, conduct validation experiments, maintain appropriate logbooksAssist in set up and maintenance of laboratory and EMS systemExecute other duties as may be required Qualifications:NA., post-secondary diploma in scientific, healthcare or pharmaceutical field, or NA 2 years' experience in a clinical research environment preferably including BE and Ph 1- IV studies, EEC is desirableProven solid project planning/coordination/management skillsStrong analytical and problem solving skillsExcellent organizational skills, detail oriented, efficient and able to multi-task and prioritize effectivelyExcellent interpersonal skillsStrong written and verbal communication skillsGood trouble-shooting and decision making skills, able to escalate response to situations when relevant Required experience:Clinical Research : 2 years Required education:Bachelor's
We are a full-service Clinical Research Organization (CRO) with a strong and highly experienced scientific team that is eager to partner with industry. Inflamax Research provides a broad range of services in all areas of clinical trial research to assure the successful completion of both R&D and marketing studies. We collaborate with academia and the scientific community to continuously develop, improve and publish innovative methods, models and standards.