Senior Clinical Data Manager

Dianthus Therapeutics, Inc.

Senior Clinical Data Manager overseeing data management activities for clinical trials. Ensuring delivery of high-quality, regulatory-compliant data and collaborating with cross-functional teams.

Posted 7/30/2026full-timeRemote • 🇺🇸 United StatesSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical data management, ensuring high-quality, regulatory-compliant data delivery while collaborating effectively with cross-functional teams and external partners. Possesses a strong understanding of drug development processes and GCP guidelines.

Highest-signal resume keywords

Clinical Data Management ExperienceData Analytics PlatformsGCP Guidelines KnowledgeCross-Functional CollaborationDrug Development Processes

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Data ManagementData Quality AssuranceData IntegrationData AnalysisRegulatory Compliance

Soft Skills

Detail-OrientedStrong Communication SkillsRelationship BuildingSelf-MotivatedCollaborative Teamwork

Tools & Technologies

DM Related SystemsClinical Trial Management SystemsData Analytics Tools

Industry Keywords

Clinical TrialsSponsorCROClinical ResearchDrug Development

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

You will oversee all clinical data management activities and deliverables from study start-up through database lock and closeout across multiple clinical trials.
Working independently with cross-functional teams and external partners, you will ensure the delivery of complete, accurate, high-quality, and regulatory-compliant data to support study reporting, publications, and regulatory submissions.
This role requires a balance of strong operational execution and innovative thinking to advance data quality, integration, and analysis in support of clinical development goals.

Requirements

What you’ll need

Bachelors degree in life sciences required
Minimum of 5 years of clinical data management experience in Sponsor and/or CRO setting
Strong understanding of DM related systems, technologies and standards including data analytics platforms
Comprehensive knowledge of drug development and clinical research processes, GCP guidelines and regulations related to clinical data management
Self-motivated and able to work autonomously as well as take direction and work within a high-functioning and collaborative team environment
Detail-oriented with strong verbal and written communication skills
Ability to build relationships internally and with external partners
Highest levels of professionalism, confidence, personal values and ethical standards.

Benefits

Comp & perks

We are open to you working remotely.