Psychiatry and neurology among other therapeutic areas rely on subjective clinician-reported outcome measures that require specialized solutions to ensure endpoint reliability and optimize signal detection potential
Rater Station®

Control endpoint measure risk factors
Reduce scale administration errors
Pre-set workflows, on-screen guidance, and automated scoring validation ensure that scales are administered and scored correctly
Improve data reliability
Prevent missing or incomplete data and transcription errors; build regulatory-compliant audit trails
Optimize subjective assessments
Reduce inter- and intra-rater variability with integrated quality monitoring, and capture audio/video interviews for expert central review/ratings
Why choose Rater Station?
Automated Scoring
Automated scoring validation when applicable
On-Screen Guidance
On-screen guidance and alerts, helping raters to correctly administer scales
Edit Checks
Flexible and customizable edit checks and notifications
Audio/Video Capture
Integrated and secure audio/video capture of interviews that can be reviewed by independent expert clinicians
Deployment Flexibility
Deployment options supporting web-based or offline access to meet diverse study requirements and site capabilities
Rater Reviews
Periodic rater reviews for quality control
Intuitive Charts
Analytics highlighting outlying data patterns color-coded graphs and intuitive charts
Audit Trail
An audit trail that captures data modifications made prior to submission
Electronic vs paper
Clinician-reported outcomes (ClinROs) that use paper make studies susceptible to human error and missing data. Our Electronic Clinician Ratings solution improves data quality and endpoint reliability through intelligent features that proactively detect scoring and administrative errors prior to submission, reducing errors by up to 80% compared to paper and form-based eCOA.
The specialist partner for your complex ClinRO trials
Trust Signant to ensure your enrolled patients meet eligibility requirements, and raters provide consistent and accurate assessments with minimal variability to drive high quality assessments and scoring throughout your study
Dawie’s deep expertise across multiple therapeutic areas, multinational development leadership, and experience in associated commercial growth supports the expanding impact of the Signant Science and Medical team. Dawie joins us from AES, where he served as Chief Medical Officer for five and a half years. Prior to AES, he held various research and senior leadership roles at Parexel for over 15 years, developing and implementing medical scientific focused business strategies across the early phase space. Dawie holds MBA and MBChB MBA (Medicine and Business) degrees from University of the Free State, South Africa. We are rightly proud of our science and medical heritage and how it has contributed to – and continues to – position us as leaders in our industry. Building on the therapeutic approach to our sales pipeline, the development of our offerings across as many therapeutic areas as possible continues under Dawie’s leadership. Originally hailing from South Africa, Dawie is based in the UK.
Dawie’s deep expertise across multiple therapeutic areas, multinational development leadership, and experience in associated commercial growth supports the expanding impact of the Signant Science and Medical team. Dawie joins us from AES, where he served as Chief Medical Officer for five and a half years. Prior to AES, he held various research and senior leadership roles at Parexel for over 15 years, developing and implementing medical scientific focused business strategies across the early phase space. Dawie holds MBA and MBChB MBA (Medicine and Business) degrees from University of the Free State, South Africa. We are rightly proud of our science and medical heritage and how it has contributed to – and continues to – position us as leaders in our industry. Building on the therapeutic approach to our sales pipeline, the development of our offerings across as many therapeutic areas as possible continues under Dawie’s leadership. Originally hailing from South Africa, Dawie is based in the UK.
Ed Pollack serves as Chief Technology Officer where he steers strategy and oversees delivery of the products and systems underpinning Signant’s growth strategy. He is responsible for driving high-performance, cross-functional teams across several disciplines and leading the development and optimization of clinical trial solutions for Signant’s life sciences customers across the globe.
Ed joins Signant from Elsevier, a leader in helping healthcare professionals advance science and improve patient outcomes, where he served as vice president of technology. His experience there, as well as his extensive background in software engineering, ensure Signant is prepared with the leadership and vision to continue scaling through accelerated growth while delivering industry-leading solutions to customers.
Prior to Elsevier, Ed held technology leadership roles at several companies focused on supporting the regulatory business process of global life sciences companies.
Ed holds a Bachelor of Business Administration in Computer Science from Temple University.

Comprehensive Technology
Purpose-built for complex clinician-reported outcome measures, our proprietary technology offers advanced electronic clinician rating capabilities with flexible deployment options

Endpoint Reliability
Our internal clinicians and global network of independent central reviewers and raters are trained, qualified, and regularly calibrated to drive the highest levels of endpoint reliability and standardized assessment quality

Scientific Consulting
Protocol and scale consultations help you navigate the complexities of electronic clinician ratings, including obtaining licenses and validating translations

Actionable Analytics
Clinically-driven proprietary algorithms and in-depth analysis and interpretation to identify data quality risks, providing early detection and proactive remediation to protect endpoint reliability and optimize signal detection
Explore associated solutions and services

Rater Training & Qualification
A proven approach to ensure scoring consistency & endpoint quality

PureSignal Analytics
Proactively detect and mitigate endpoint data quality risks to safeguard your signal detection

Scale & License Management
Simplify selecting and using appropriate clinical outcome assessments for studies

Central Rating & Consulting
Identify and act on data trends with collaborative action planning
FAQs
What is an endpoint in clinical research?
Clinical endpoints are measurable outcomes used to address the objectives of a clinical trial, such as survival, decreased pain, or the absence of disease.
What is a primary endpoint in clinical trial?
Primary endpoints measure outcomes that will answer the most important question being asked by a trial, such as whether a new treatment is better at preventing disease-related death than the standard therapy. Secondary endpoints answer other relevant questions about the same study, such as patient-reported outcomes on their quality of life.
How do you ensure data quality in clinical research?
Innovative technology, routine training, and guidance from experienced subject matter experts help researchers ensure high data quality. Signant offers all of those solutions and services, catering to the unique needs of sponsors and regulators.
Want to learn more?
Deploy Rater Station to your study to collect reliable clinician-rated endpoint data – contact our team today