Clinical Trial Associate
Description
We're looking for a Clinical Trial Associate, working in Biotechnology/Medical Devices industry in Madison, New Jersey, United States.
Job description:
? Support study feasibility activities and perform database/web searches for sites as needed.
? Work closely with the Site Start Up (SSU) and ensure all study related regulatory and financial documents are collected and reviewed in support of study activation.
? Organize and maintain project working files and track critical documents. Report discrepancies to the appropriate clinical team member in a timely manner.
? Reconcile and transmit all essential documentation to CDIC as per Forest policy.
? Track and assist with processing site/vendor payments. Follow up on any issues as required.
? Collect and track patient enrollment information and update study management reports as necessary.
? Participate in testing of specifications and edit checks for internal (i.e. electronic data capture (EDC) and external (e.g. Interactive Voice/Web Response Systems (IVRS/IWRS), laboratory vendors) systems.
? Assist senior team members with in the planning, preparation, and on-site support of investigators meetings.
? Generate reports in various applications to assist the Clinical Scientist to perform clinical data review.
? Assist with ongoing data review and discuss comments with the clinical study team as needed.
? Assist with the preparation and distribution of meeting agendas and minutes. Actively participate in team meetings.
? Provide input and support in the development and distribution of monthly site newsletters.
? Support the Regional Site Managers by providing study related information and supplies, as requested.
? Communicate with IRBs and outside vendors to provide information and/or resolution to specific requests/issues.
? Support and correspond with sites to identify site specific needs (e.g. order and track study drug/other trial related supplies).
Apply Now
We're looking for a Clinical Trial Associate, working in Biotechnology/Medical Devices industry in Madison, New Jersey, United States.
Job description:
? Support study feasibility activities and perform database/web searches for sites as needed.
? Work closely with the Site Start Up (SSU) and ensure all study related regulatory and financial documents are collected and reviewed in support of study activation.
? Organize and maintain project working files and track critical documents. Report discrepancies to the appropriate clinical team member in a timely manner.
? Reconcile and transmit all essential documentation to CDIC as per Forest policy.
? Track and assist with processing site/vendor payments. Follow up on any issues as required.
? Collect and track patient enrollment information and update study management reports as necessary.
? Participate in testing of specifications and edit checks for internal (i.e. electronic data capture (EDC) and external (e.g. Interactive Voice/Web Response Systems (IVRS/IWRS), laboratory vendors) systems.
? Assist senior team members with in the planning, preparation, and on-site support of investigators meetings.
? Generate reports in various applications to assist the Clinical Scientist to perform clinical data review.
? Assist with ongoing data review and discuss comments with the clinical study team as needed.
? Assist with the preparation and distribution of meeting agendas and minutes. Actively participate in team meetings.
? Provide input and support in the development and distribution of monthly site newsletters.
? Support the Regional Site Managers by providing study related information and supplies, as requested.
? Communicate with IRBs and outside vendors to provide information and/or resolution to specific requests/issues.
? Support and correspond with sites to identify site specific needs (e.g. order and track study drug/other trial related supplies).
Apply Now