Clinical Monitor (CRA) - Neurosciences - Remote - 139341

Benefits

Qualifications

• •Demonstrated self-discipline and sound, independent judgment completing complex assignments
• •Monitors must be able to work independently as well as a team to ensure the success of our trials
• •ADCS monitors function as ambassadors to ADCS sites and therefore must possess the ability to make independent judgments that will not endanger the integrity of the trial, trial data, or most importantly, participant safety
• •Thorough knowledge and ability to apply all relevant Federal, state, and university regulations, policies, and federal guidance documents
• •As stated previously, monitors must be current with CITI training, GCP, and have a thorough knowledge of each of the trial protocols that they will be monitoring
• •Knowledge of FDA regulations and regulatory compliance is also critical as it pertains to each study
• •Thorough knowledge and experience with quantitative and qualitative research design; scientific research concepts and terminology
• •ADCS monitors are expected to contribute to the design of the monitoring plan for each trial, and therefore, must have experience and knowledge of trial and research designs, particularly those related to the monitoring of the trial/study
• •Demonstrated proficiency in public speaking, and writing
• •ADCS monitors must have exceptional communication skills since they work very closely with site personnel, which includes study coordinators, nurses, doctors, administrators, etc
• •Strong experience with Electronic Data Capture (EDC) systems, Clinical Trial Management Systems (CTMS), and Trial Master Files (eTMF)
• •Understanding of Risk-Based Monitoring (RBM) and remote monitoring platforms, which are increasingly standard in modern trials
• •Excellent ability to organize/prioritize workload effectively to meet deadlines in an environment with multiple interruptions and changing priorities
• •Meticulous attention to detail
• •Efficiently juggling multiple sites across different time zones, including domestic or international travel
• •Must be able to work various hours and locations based on business needs
• •Must be willing to travel up to 80% of the time
• •Employment is subject to a criminal background check
• •Job offer is contingent upon satisfactory clearance based on Background Check results
• •Federal, state, or local public health directives may impose additional requirements
• •If applicable, life-support certifications (BLS, NRP, ACLS, etc.) must include hands-on practice and in-person skills assessment; online-only certification is not acceptable
• •Misconduct Disclosure Requirement: As a condition of employment, the final candidate who accepts an offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; or have filed an appeal of a finding of substantiated misconduct with a previous employer
• •19 more items(s)

Responsibilities

• •8-Hour Shifts, Monday-Friday
• •The ADCS provides expertise in developing Alzheimer's disease related protocols and is the coordinating center for multiple clinical trials of varying sizes and complexity under subcontracts funded by NIH and clinical trial agreements with industry partners
• •Uses skills as a seasoned, experienced research compliance professional with a full understanding of industry practices and organization policies / procedures to apply FDA, federal, state, and university regulations, policies, and guidelines, and promote best practices
• •Interacts frequently with investigators, persons in other organizational departments, and frequently with site staff and PIs outside the University
• •Interactions require the use of tact and independent judgment, knowledge of standards and best practices, and counseling to resolve a wide range of research compliance issues
• •Demonstrates good judgment in selecting methods and techniques for obtaining solutions
• •Errors or omissions may ultimately place research participant at undo risk and / or compromise the institution's assurance of regulatory compliance with the federal government
• •They frequently interface with sites and therefore represent the ADCS while monitoring sites, and are on the front lines in identifying and resolving questions or problems that sites may encounter
• •CMs work under the general supervision of the ADCS monitor manager
• •CMs are responsible for managing research trials for approximately 60 sites within the ADCS consortium conducting multiple clinical trials in Alzheimer’s Disease (AD) at centers located throughout the United States and Canada
• •CMs are responsible for adherence to FDA regulations, study protocols, SOPs, GCP and ALCOA guidelines, for all sites conducting ADCS studies
• •They are also responsible for ensuring the accuracy and integrity of data integrity at sites as well as appropriate documentation as outlined in FDA guidelines for clinical trials
• •CMs manage clinical research sites, identifying and introducing new monitoring procedures to optimize team performance, overseeing the execution of the Standard Operating Procedures, protocol implementation, and overseeing study close-out in order to maintain regulatory compliance and standardize ”Best Practices” at each site
• •CMs define goals and progress, contribute innovative solutions to implementation of studies, and determine clinical needs of research projects
• •Other duties include developing productivity and data management tools and working with other groups to provide operational and strategic support
• •CMs independently conduct study site visits that include training and leading site personnel (PIs, study coordinators, physicians) in protocol procedures and compliance, implementation, and administration of neuropsychological tests
• •CMs also facilitate and attend meetings as well as participate in conference calls with trial Project Directors and other ADCS team members as required
• •They are also frequently asked to present at Investigator Meetings, which requires speaking to diverse and large audiences
• •Monitors must also have excellent writing skills since they are required to complete and submit monitoring reports related to each of their site visits
• •This documentation is essential to the conduct of each trial
• •Monitors should be aware of COI in regards to ADCS disclosure reporting to ensure that sites are not approved to begin screening participants until COI has been reviewed and no conflicts have been determined/and or have been resolved
• •18 more items(s)