# Clinical Research Associate **Company**: Fortrea **Work arrangement**: hybrid **Experience**: senior **Job type**: full-time **Category**: Healthcare **Industry**: Healthcare **Apply**: https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Beijing/FSO-CRA-II--Beijing-Tianjin-Shijiazhuang-Zhengzhou-Ji-nan-Harbin-Changchun-Shenyang-Xi-an-_266206?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply **Canonical**: https://yubhub.co/jobs/job_a45ab4c5-e1a ## Description We are seeking a Clinical Research Associate to manage clinical studies according to Fortrea's Standard Operating Procedures, ICH GCP Guidelines, and Sponsor requirements. **Responsibilities:** - Conduct site monitoring responsibilities for clinical trials, including Pre-study, Site Initiation, Process Monitoring, Routine Monitoring, and Close-out Visits - Prepare and implement project plans related to Clinical Monitoring responsibilities - Ensure the protection of subjects by verifying that informed consent procedures and protocol requirements are adhered to - Safeguard data integrity by careful source document review, source document verification, query generation, and resolution against established data review guidelines - Confirm Site Regulatory documents and applicable eTMF/Sponsor Documents are complete and current throughout the duration of the trial - Guarantee that the study Investigational Product inventory and accountability is accurate and that study materials are stored securely and per protocol requirements - Ensure adherence to global quality control and CRA performance metrics - Ensure audit readiness at site level - Act in the project role of a Lead CRA as assigned **General On-Site Monitoring Responsibilities:** - Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter subjects/patients into the study - Ensure the protection of study subjects or patients by performing eligibility review, verifying that screening, informed consent procedures and protocol requirements are adhered to - Ensure the integrity of the source data reported by careful source document review - Monitor data for missing or implausible data - Ensure study data completeness, accuracy, consistency, and compliance - Identify deficiencies, deviations and discrepancies, and initiate corrective action as required - Ensure the resources of the Sponsor and Fortrea are spent wisely by performing the required monitoring tasks in an efficient manner - Travel, including air travel, may be required and is an essential function of the job - Prepare and submit accurate and timely trip reports - Independently perform eCRF review, 100% source data verification, query generation and resolution against established data review guideline with or without direct supervision - Assist with the administration of clinical research projects, recruiting investigators, collecting investigator documentation and site management - Update, navigate, and maintain Fortrea or study/Sponsor-specific trial management tools/eClinical systems - Track IP shipments and supplies, as needed - Track and follow-up on serious adverse events as assigned - Work closely with the study team, align monitoring to critical study timelines ensuring study deliverables are met - Prepare and implement study-specific monitoring plans and site Initiation slides, as assigned - Attend investigators' meetings, project team meetings and teleconferences, and others as needed - Present training content for site initiation - Assist with training of new employees **Qualifications:** - University or college degree, or certification in a related allied health profession from an appropriately accredited institution - Thorough understanding of ICH GCP Guidelines and understanding of local regulatory requirements - Thorough knowledge of monitoring procedures - Basic understanding of the clinical trial process - Fluent in local office language and in English, both written and verbal **Experience:** - A minimum of 2 years of Clinical Monitoring experience - Ability to monitor study sites independently according to monitoring plan, project requirements, SOPs, and ICH GCP guidelines - Ability to work with minimal supervision - Have an understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs **Preferred Qualifications:** - Thorough working knowledge of Fortrea SOPs for site monitoring - One (1) or more additional years of experience in a related field - Phase I monitoring experience - Life Science or Nursing qualification - Specific skills, systems, certifications, and/or licenses preferred **Physical Demands/Work Environment:** - Must be able to sit at a computer for long periods of time - Must be able to use hands to finger, handle or touch objects, tools or controls, including a computer keyboard, for up to 8 hours per day - Standard office and/or home working environment - Clinical Research Unit and hospital environment (administrative only) - Risk of eye strain - Will involve outside of normal office hours as required by the role - Travel Requirement is 60% of the time (traveling to study sites) ## Skills ### Required - ICH GCP Guidelines - Clinical Monitoring - Source Document Review - Data Integrity - Regulatory Compliance ### Nice to have - Fortrea SOPs - Phase I monitoring - Life Science or Nursing qualification - e-clinical systems --- Source: [Apply at fortrea.wd1.myworkdayjobs.com](https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Beijing/FSO-CRA-II--Beijing-Tianjin-Shijiazhuang-Zhengzhou-Ji-nan-Harbin-Changchun-Shenyang-Xi-an-_266206?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)