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Field Clinical Research Associate (Remote). Clinical Research Associate. Working with a moderate level of remote guidance and direction, is accountable for clinical study site maintenance, data and source documentation collection, as well as field monitoring of clinical trials.. Focus is on site management activities such as collection of essential documents, identifying and obtaining missing data, data corrections, reviewing adverse events and protocol deviations.. Resources will be monitoring academic centers so experience as a monitor is a must such as at Mt. Sanai, NYU, Columbia, Cornell - be prepared to expound on the job itself when we meet with suppliers and provide detail so they know how to source for candidates

clinical research associate

Description <ul><li> Home </li><li> Search Jobs </li><li>Job Description </li></ul>Field Clinical Research Associate (Remote) Contract: North Chicago, Illinois, US Salary: $65.00 Per Hour Job Code: 339940 End Date: 2024-03-14 Days Left: 5 days, 2 hours left Apply To discuss more about this job opportunity, please reach out to Chitrank Rastogi (LinkedIn URL - ), email your updated resume at Email - or give me a call at . Thank you! Pay Range - $60 to $65/hr. (negotiable) Job Description: Job Roles & Responsibilities: <ul><li>Working with a moderate level of remote guidance and direction, is accountable for clinical study site maintenance, data and source documentation collection, as well as field monitoring of clinical trials.</li><li>Ensures compliance to the study protocol, and Monitoring Plan by ensuring completeness and accuracy of data as well as compliance with domestic and international regulations, Good Clinical Practices, applicable regulatory standards, and SJM Standard Operating Procedures.</li><li>Able to solve a range of straightforward problems and analyze possible solutions using standard procedures.</li><li>Focus is on site management activities such as collection of essential documents, identifying and obtaining missing data, data corrections, reviewing adverse events and protocol deviations.</li><li>Maintains accurate, detailed and complete records of monitoring visits. In consultation with the assigned Field Clinical Engineer or designee and/or appropriate in-house personnel, coordinates the initiation of the clinical site.</li><li>Work requires the application of theoretical principles and creative/analytical techniques.</li><li>Identifies and routinely uses the most effective, cost efficient and best practices to execute processes; continually evaluates their effectiveness and appropriateness.</li><li>Stays abreast of and consults on technical advancements.</li><li>Promotes the process of continuous quality improvement and risk management, and coordinates solutions for technical and project issues.</li><li>Exercises judgment in planning and organizing work; monitors performance and reports status. </li></ul>Essential Functions: <ul><li>Monitors clinical studies at sites in an assigned territory (and others as requested) to ensure compliance with applicable regulatory requirements, Good Clinical Practice, and accuracy standards inclusive of site initiation, periodic, and close-out visits.</li><li>Ensures both regulatory and clinical protocol compliance is maintained for all assigned clinical projects. </li></ul>This may include, but is not limited to: <ul><li>Reviewing data and source documentation from investigational sites for accuracy and completeness</li><li>Ensuring adverse events and protocol deviations are reported in an efficient manner</li><li>Ensuring that device complaints and malfunctions are reported according to SJM Policies and Procedures</li><li>Resolving and/or facilitating resolution of problems including identification of cause and actions to prevent reoccurrence3. Coordinates with study teams, field clinical engineers or designee to:</li><li>Enroll sites into new and ongoing clinical studies </li></ul>Manager Comments: <ul><li>Resources will be monitoring academic centers so experience as a monitor is a must such as at Mt. Sanai, NYU, Columbia, Cornell - be prepared to expound on the job itself when we meet with suppliers and provide detail so they know how to source for candidates</li><li>Must have a clinical research background </li></ul>Job Requirement <ul><li> Clinical Research Associate </li><li> CRA </li><li> Clinical Research </li><li> Clinical Study </li><li> Monitoring </li><li> site management </li><li> Medical Device </li><li> in vitro </li><li> IVD </li></ul>Reach Out to a Recruiter <ul><li>Recruiter</li><li>Email</li><li>Phone </li><li>Chitrank Rastogi </li></ul>Apply Now

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