Work as Operations Clinical Data Manager at Signant Health

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.

Post : Clinical Data Manager - Operations

Job Description
About the Role
The 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 to ensure 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.

Key Accountabilities - Function
• Collaborate across functional groups to address technical issues impacting quality, drive forward technical initiatives within Data Management
• Provides data management guidance to internal project team members and customers
• Communicates with internal project team members and customers on all aspects of data management activities performed for a study
• Authors data management plans (DMP) and data transfer specifications (DTS)
• Performs user acceptance testing on reports and automated data checks programmed to support the data cleaning activities specified in the DMP
• Reviews, makes decisions, and acts upon output from automated data checks
• Facilitates risk assessments for mid-study changes
• Verifies data extracts against the DTS
• Provides proactive data monitoring per contractual obligations
• Facilitates and verifies data clarifications, data corrections, and external data reconciliation
• Contribute to the development and update of process improvements that reduce processing times, increase quality, mitigate operations risks, improve team performance, and meet departmental objectives and corporate objectives
• Communicates effectively within a multi-disciplinary project team to complete assigned tasks on time and within budget
• Assists in developing and improving Standard Operating Procedures (SOPs), Working Instructions and Best Practices

Candidate Profile
Essential :
• BA/BS degree in a relevant field (Medicine, Statistics, Computer Science) or equivalent work experience
• Strong verbal and written communication skills
• Ability to complete high quality technical documentation
• Demonstrate extreme attention to detail and organization in all aspects of work
• Ability to quickly learn and apply new skills, procedures and approaches.
• Demonstrated ability to meet very short deadlines & multi-task in an extremely fast-paced work environment with little direct supervision
• Proven ability to work both independently and in a team-oriented environment, providing back-up support to team members & establishing/maintaining effective work relationships with co-workers within and across functional areas
• Previously demonstrated proactive and positive approach to tasks and projects overall, as well as to the types of scheduling & process changes that are inherent in a fast-paced business

Desirable :
• 5+ years of professional experience in the clinical trials data management field
• Experience in providing data management services in the clinical trials industry
• Proficient in Access, Excel, and other office software technologies and applications.
• Proven ability to handle multiple competing priorities in a fast-paced work environment with minimal direct supervision.
• Familiarity with 21 CFR Part 11 or experience in a regulated environment desirable

Additional Information
Experience : 5+ years
Qualification : BA/BS degree in a relevant field
Location : Noida, Uttar Pradesh
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Operations
End Date : 20th September 2026