About Signant Health
At Signant Health, we help bring life-changing treatments to patients faster. We are a global evidence generation company that supports clinical trials with smart technology, scientific expertise, and hands-on operational support — so better data leads to better decisions in healthcare. We embrace AI and advanced technologies to enhance every aspect of what we do, from data analysis to operational efficiency.
Our teams work at the intersection of science, technology, and patient experience, delivering digital solutions powered by AI innovation that make clinical trials more efficient, more accurate, and more accessible around the world. Trusted by leading pharmaceutical companies and CROs, our platforms and services support studies across 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 — including the opportunity to work with cutting-edge AI technologies — you will find purpose and opportunity at Signant Health.
About the Role
The Associate Clinical Data Manager is responsible for working with the Clinical Data Management team and other internal project team members to provide data management services for our customers, ensuring on-time and accurate deliverables. Responsibilities include providing data management guidance to internal project team members and customers; communicating with internal project team members and customers on all aspects of data management activities performed for a study; authoring data management documents; performing user acceptance testing on data management deliverables; and facilitating and verifying data clarifications and data changes.
Shift: This role requires working a night shift on a rotational basis.
KEY ACCOUNTABILITIES – Function
Develop and maintain the Data Management Plan (DMP).
Develop and maintain study-specific Data Cleaning / Reconciliation reports and validation plans.
Provide weekly data management status updates to clients and internal Project Managers.
Work with the internal Delivery team to define data management timelines, ensuring DM milestones are met.
Develop other study-specific documentation manuals, including but not limited to the Maintenance Guide (MG), as necessary.
Conduct study-specific trainings with internal Data Coordinators and Data Reviewers prior to release of the Data Management Plan initiatives.
Adhere to Signant Health Standard Operating Procedures for all data management responsibilities.
Identify areas of opportunity for improvement in the end-to-end Data Management process, driving out waste, increasing productivity, and delivering quality.
Support delivery of improvements in the Data Management process by participating in small group activities, kaizen events, and Lean Six Sigma projects when necessary.
Work a night shift on a rotational basis to support study and client needs across time zones.
Decision Making and Influence
Collaborate with clients and internal Delivery teams to develop and maintain protocol-specific monitoring report specifications.
Collaborate with clients and internal Data Coordinators and Data Reviewers to generate a study-specific tool for flagging discrepancies between the client IVR/EDC and TrialManager outputs.
Collaborate with clients and the internal Technical Client Services team to conduct protocol reviews and identify protocol-specific device design and eligibility criteria.
Collaborate with clients and the internal Technical Client Services team to define protocol-specific report(s) as necessary.
Collaborate with the internal validation team to define detailed test cases for clinically significant reports.
KNOWLEDGE, SKILLS & ATTRIBUTES
Essential:
BA/BS degree in a relevant field (Medicine, Statistics, Computer Science) or equivalent work experience.
Technical aptitude and ability to complete high-quality technical documentation; ability to understand and work…