Clinical Development Specialist -Medical Affairs (Remote)
About the position
A Clinical Development Specialist will work with Quest Medical and Laboratory Directors and their staff, Clinical Development management and staff, external scientific and clinical administrative staff and external vendors to support S & I clinical development research efforts. The Clinical Development Specialist is responsible for oversight of all operational aspects of clinical studies including; clinical study initiation activities, site selection and training efforts, study documentation, study site monitoring, query resolution, data monitoring and data flow, flow of specimens between sites, study site payment activities, study close down. This person will report to Clinical Development Management. This professional can work in a remote capacity and must be located in the US.
Responsibilities
• Oversight of all operational aspects of clinical studies
• Clinical study initiation activities
• Site selection and training efforts
• Study documentation
• Study site monitoring
• Query resolution
• Data monitoring and data flow
• Flow of specimens between sites
• Study site payment activities
• Study close down
Requirements
• Must be located in the US
Apply tot his job
Apply To this Job
A Clinical Development Specialist will work with Quest Medical and Laboratory Directors and their staff, Clinical Development management and staff, external scientific and clinical administrative staff and external vendors to support S & I clinical development research efforts. The Clinical Development Specialist is responsible for oversight of all operational aspects of clinical studies including; clinical study initiation activities, site selection and training efforts, study documentation, study site monitoring, query resolution, data monitoring and data flow, flow of specimens between sites, study site payment activities, study close down. This person will report to Clinical Development Management. This professional can work in a remote capacity and must be located in the US.
Responsibilities
• Oversight of all operational aspects of clinical studies
• Clinical study initiation activities
• Site selection and training efforts
• Study documentation
• Study site monitoring
• Query resolution
• Data monitoring and data flow
• Flow of specimens between sites
• Study site payment activities
• Study close down
Requirements
• Must be located in the US
Apply tot his job
Apply To this Job