Associate Clinical Data Manager – Operations

Signant Health

. Work with the Clinical Data Management team and internal project team members to provide data management services for customers .

Posted 11/9/2026full-timeRemote • IndiaMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in Clinical Data Management, including the development and maintenance of Data Management Plans and study-specific documentation. Proficient in data management best practices and regulatory compliance, with strong communication and organizational skills.

Highest-signal resume keywords

Clinical Trials Data ManagementData Management Plan DevelopmentUser Acceptance TestingFamiliarity With EDC SystemsProficient In Access And Excel

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data Management DocumentationData Cleaning And ReconciliationHTML ProficiencyTechnical DocumentationProtocol ReviewTest Case DefinitionData Clarification FacilitationStudy-Specific TrainingProcess Improvement IdentificationAttention To Detail

Soft Skills

Strong Verbal CommunicationStrong Written CommunicationProactive ApproachAbility To MultitaskTeam-Oriented

Tools & Technologies

AccessExcelClinical DatabasesOffice Software Technologies

Industry Keywords

GCPGDPRMHRA21 CFR Part 11Regulated Environment

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Work with the Clinical Data Management team and internal project team members to provide data management services for customers
Ensure on-time and accurate deliverables
Provide data management guidance to internal project team members and customers
Communicate with internal project team members and customers on study data management activities
Author data management documents
Perform user acceptance testing on data management deliverables
Facilitate and verify data clarifications and data changes
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 and ensure DM milestones are met
Develop study-specific documentation manuals, including the Maintenance Guide (MG), as necessary
Conduct study-specific trainings with internal Data Coordinators and Data Reviewers
Adhere to Signant Health Standard Operating Procedures
Identify process improvement opportunities in end-to-end Data Management
Participate in small group activities, kaizen events, and Lean Six Sigma projects when necessary
Work a rotational night shift to support study and client needs across time zones
Collaborate with clients and internal teams to develop protocol-specific monitoring report specifications
Generate study-specific tools for flagging discrepancies between client IVR/EDC and TrialManager outputs
Conduct protocol reviews and identify protocol-specific device design and eligibility criteria
Define protocol-specific reports as necessary
Collaborate with the validation team to define detailed test cases for clinically significant reports

Requirements

What you’ll need

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 with HTML and different types of clinical databases
Extreme attention to detail and organization
Ability to quickly learn and apply new skills, procedures, and approaches
Ability to meet very short deadlines and multitask in an extremely fast-paced work environment with little direct supervision
Ability to work independently and in a team-oriented environment
Proactive and positive approach to tasks and projects
Proficient in Access, Excel, and other office software technologies and applications
Ability to handle multiple competing priorities with minimal direct supervision
Strong verbal and written communication skills
Willingness and ability to work a night shift on a rotational basis
Familiarity with 21 CFR Part 11 or experience in a regulated environment
3+ years of professional experience in the clinical trials data management field
Familiarity with data management best practices (GCP, GDPR, MHRA)
Familiarity with EDC systems

Benefits

Comp & perks

Opportunity to work with cutting-edge AI technologies
Meaningful work and global impact
Innovation in clinical research and digital health