Clinical Research Coordinator II - Neurology - 49993 | Washington University in St. Louis - Military Veterans

at Herc - Missouri

St. Louis, Missouri

EOE Statement: Washington University is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity or expression, national origin, genetic information, disability, or protected veteran status. Job Type/Schedule: This position is full-time and works approximately 40 hours per week.   Department Name/Job Location: This position is in the Department of Neurology.  This position is for the Medical School Campus. Essential Functions: POSITION SUMMARY: The Clinical Research Coordinator II (CRC-II) will work closely with the DIAN and DIAN-TU Cognition Core Leader, the Clinical Research Specialist for DIAN and DIAN-TU and other lab members and will be assist core personnel with site communications, vendor communications, and quality control and data verification tasks. Ideally, the CRC-II will have experience with FDA regulated clinical trials and cognitive and clinical assessment measures. DIAN and DIAN-TU are global studies with sites in EU, Asia, Australia, and North and South America. The position will involve maintaining frequent contact with raters and site coordinators at all DIAN and DIAN-TU sites, as well as with project managers and other representatives from multiple vendors. PRIMARY DUTIES AND RESPONSIBILITIES: Quality Control: One of the primary functions of the Cog Core is to perform quality control reviews of cognitive assessments and verification that these reviews were completed correctly. Because the DIAN studies are global, we work with vendors with native language expert clinicians. Vendor Communication: The CRC-II will handle several aspects of vendor communication, including maintaining frequent contact with personnel from vendors including project managers, native language experts, and other vendor personnel. Quality Control: Tracks QC processes with vendors and other core personnel to ensure timely completion. QC verification: Assists team members to ensure that QC processes are completed correctly and in accordance with Standard Operating Procedures (SOPs). Works with Cog Core members to provide timely updates of data quality. Coordinates regular audits from external vendors and organizes audit response documentation. Maintains documentation and materials for Cog Core: Assists Cog Core staff with creation and maintenance of all Cog Core documentation. Maintains cognitive assessment battery materials and equipment and works with relevant cores from DIAN and DIAN-TU to ensure that materials are up to date and versioned appropriately for all DIAN sites globally. Works with vendors to manage eCOA assessments and equipment. Works with vendors, DIAN site personnel, and Cog Core personnel to acquire and update translations for each language used in DIAN studies. Prepares and updates SOPs, work instructions, procedures manuals, and other documents for the Cog Core. Responds to external and internal audits as requested by Cog Core team to ensure compliance with ICH-GCP and 21 CFR Part 11 compliance. Acquires translations from vendors and assists with clinician review of translations. Maintains translation certification documents. Acquires and manages licenses from test publishers for proprietary cognitive measures. Rater Training Documentation: The CRC-II will be responsible for tracking and maintaining materials for a web-based rater training platform provided by a vendor. CRC-II will coordinate with Cog Core members and DIAN sites to track and maintain rater certification documents and procedures to ensure compliance with ICH/GCP standards. Tracks all rater certification and manages notification system for certification expiration. Schedules training webinars for raters and site coordinators. Works closely with Cog Core leaders and Clinical Core personnel to facilitate critical study communications with raters and site coordinators. Performs other duties incidental to the work described herein. Required Qualifications: Bachelor’s degree plus a minimum of two years of clinical research experience; a combination of relevant work and education equaling six years may substitute for this requirement. Preferred Qualifications: ICH-GCP experience, CRA experience and practical experience in SOP and CRF development. Working knowledge of techniques and methodologies used in developing, coordinating, and managing clinical research projects. Working knowledge of database management. Willing to ask for clarification or track down additional information independently. Ability to establish workflows that comply with regulatory requirements. Experience working in culturally diverse environments is highly preferred.  Candidates must be committed to the School’s goal of advancing inclusive excellence and be prepared to explain how they have been and/or will be involved in advancing this goal within WUSM. Good understanding of the operational execution of clinical protocols. Document development skills (e.g. formatting) in MS Word, Powerpoint, and Adobe Acrobat. Basic business writing skills required for protocols, amendments, memorandums, study summaries, and progress reports. Experience with various electronic data capture, web-based applications, and storage systems. Excellent communication skills (both written and oral). Ability to be clear, direct, and tactful when communicating with multiple sites (national and international), departments, staff, CROs, vendors, and investigators. Willing to travel as necessary (i.e. investigator meetings, seminars or vendor meetings, etc.). Salary Range: The hiring range for this position is $48,131 - $60,174 annually. Pre-Employment Screening: All external candidates receiving an offer for employment will be required to submit to pre-employment screening for this position. Current employees applying for a new position within the university may be subject to this requirement. The screenings will include a criminal background check and, as applicable for the position, other background checks, drug screen, employment and education or licensure/certification verification, physical examination, certain vaccinations and/or governmental registry checks. All offers are contingent upon successful completion of required screening. Benefits: This position is eligible for full-time benefits.  Please click the following link to view a summary of benefits: . Internal Applicant Instruction: This position is grade C10. Please attach a copy of your most current signed performance evaluation (completed within the last 18 months) to your online account.  If you have not received a performance evaluation, you may provide two current signed letters of recommendation (written within the last 18 months), preferably to include one letter from either a current or recent former supervisor.  To attach these documents, go to:  My Career Tools, Add Attachment, Attachment Type – Performance Reviews or Letters of Recommendation.