About signant healthat signant health, we help bring life-changing treatments to patients faster. We are a global evidence generation company supporting clinical trials through smart technology, scientific expertise, and hands-on operational support — because better data leads to better healthcare decisions. Our teams work at the intersection of science, technology, and patient experience, delivering digital solutions that make clinical trials more efficient, accurate, and accessible worldwide. Trusted by leading pharmaceutical companies and cros, our platforms and services support studies in more than 90 countries and have contributed to hundreds of new drug approvals. If you are motivated by meaningful work, global impact, and innovation in clinical research and digital health, you will find purpose — and opportunity — at signant health. ing sector - a high-growth, dynamic company in an extraordinary industry.about the role the central quality reviewer (cqr) is responsible for the services/tasks to deliver defined requirements and meet company strategic objectives. The cqr provides data oversight for signant health rater training, endpoint reliability, and quality assurance programs. The cqr will provide clinical analysis for scales used as study endpoints to detect the degree of administration and scoring calibration to standard training principles and best practice. The cqr will provide email and telephone remediation to investigators as needed to recalibrate to study standards. The cqr may interview study participants or provide independent scoring of endpoint scales on submitted audio or video files.what you will do conducts all activities in full accordance with good clinical practice guidelines. Contributes to training, calibration exercises, and quality control procedures for respective projects assigned. Evaluates data submitted in accordance with rater training program, e.g., interview skills, and endpoint reliability programs and contacts raters, as appropriate, to gather additional information and provide feedback. Ensures consistency of review and remediation process and resolves ambiguities in collaboration with study team and other stakeholders. May interview subjects and/or informants according to scale and protocol specifications; may provide independent scoring data based on review of audio and video files. Monitors and conducts quality review of internal and external cqrs activities by reviewing both the data and documentation entered by cqrs as indicators of their performance. Works with clinical team to ensure study start up is completed for the program, including the development of materials for cqr onboarding, training, quality assurance, etc. Proactively identifies and escalates potential issues appropriately. Supports the development of site relationships to ensure that the site staff are trained and calibrated to the study-specific and universal standards. Communicates with investigational site staff providing feedback and instruction, as needed.decision making and influence facilitates and maintains team and corporate culture of collegiality, respect, and professional support. Capable of weighing risks and making decisions that align with signant health values and strategy. Manage customer escalations effectively, withfollow up and closure.preferred qualifications master's degree, m.d., ph.d., psy.d, pharm.d., in healthcare-related field, with one year of clinical experience, which includes administration of psychiatric and/or cognitive scales or bachelor's degree or rn with 2 years of clinical experience, which includes administration of psychiatric and/or cognitive scales. Must be comfortable providing investigator and peer remediation. Demonstrates a significant attention to detail. Must be comfortable working in a virtual, remote environment with individuals from diverse countries, languages, and cultures. Exhibited strong analytical, organizational, and creative problem-solving skills. Deep knowledge of psychiatric and/or cognitive scales. Basic knowledge of statistics. Able to work with and interpret data and numbers. Excellent problem and/or dispute resolution skills. Must have excellent written, time management, communications, decision making, human relations and organizational skills, including fluency in english (will be required to write, speak, and understand english to conduct day-to-day business). Experience with at least one of the following scales is mandatory: clinical dementia rating (cdr) mini mental state examination (mmse) structured clinical interview for dsm disorders (scid) neuropsychiatric inventory – clinician (npi-c)why signant health? At signant health, your work has real impact. Everything we build, support, and deliver helps advance clinical research and bring new treatments to patients faster — improving lives around the world. Our teams combine science, technology, and operational expertise to solve complex clinical trial challenges, and every role contributes to that mission. We offer a collaborative, global environment where you can grow your career while working alongside experts across clinical, technology, data, and operations, with opportunities to learn, take ownership, and drive meaningful innovation — not just maintain the status quo. If you are looking for purpose-driven work, smart colleagues, and the opportunity to help shape the future of clinical research and digital health, signant health is the place to do it.location:santiago, rm, chile language:resumes must be submitted in english. At signant health, accepting difference isn't enough—we celebrate it, we support it, and we nurture it for the benefit of our team members, our clients and our community. Signant health is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or veteran status.#li-im1