Clinical Data Manager

Telix Pharmaceuticals Limited

. Ensure the integrity, accuracy, and compliance of clinical trial data with study and regulatory requirements, SOPs, and CDISC data standards .

Posted 9/24/2026full-timeRemote • United StatesMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical trial data management, ensuring compliance with GCP and CDISC standards while overseeing data quality and integrity throughout the trial lifecycle. Proficient in managing multiple vendors and timelines, with a strong focus on data collection optimization and documentation.

Highest-signal resume keywords

Clinical Trial Data ManagementGCP ComplianceCDISC StandardsData Management PlansECRF Specifications

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data CleaningData Quality OversightEDC DevelopmentData Transfer AgreementsUAT PlansECRF Completion GuidelinesData Review PlansEdit Check SpecificationsStudy Protocol DevelopmentRegulatory Compliance

Soft Skills

Attention to DetailOrganizational SkillsCollaborationAdaptabilityCommunication

Industry Keywords

Health Information ManagementLife SciencesClinical Data ManagementGlobal Clinical TrialsSDMTCDASH

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Ensure the integrity, accuracy, and compliance of clinical trial data with study and regulatory requirements, SOPs, and CDISC data standards
Oversee data quality for Telix clinical trials
Ensure EDC development meets study requirements
Oversee data cleaning activities and manage external data transfers
Lead data management activities for assigned clinical trials from study start-up through database lock and study close-out
Optimize data collection, flow, and access across EDC and non-EDC sources
Act as primary data management subject matter expert for assigned trials
Oversee EDC build activities, including DMPs, data review plans, specifications, UAT, and eCRF completion guidelines
Oversee data entry, cleaning activities, and eTMF data management documentation
Liaise with external vendors regarding timelines, deliverables, and data transfers
Assist with review of data-related deliverables and development/review of protocols and SAPs
Support audits, inspections, study kick-off meetings, and internal Clinical Data Management initiatives
Ensure compliance with GCP, CDISC standards, and applicable regulations

Requirements

What you’ll need

Bachelor’s degree in Health Information Management, Life Sciences or equivalent work experience
Advanced degree preferred
3+ years of experience in clinical trial data management
Minimum of 1 year of experience independently leading data management activities for complex global clinical trials
Ability to oversee multiple vendors and manage strict timelines for multiple global complex clinical trials
Experience creating eCRF specifications, edit check specifications, Data Management Plans, Data Review Plans, eCRF Completion Guidelines, UAT plans and test scripts, and data transfer agreements
Accuracy, strong attention to detail, highly developed organizational skills, prioritization, sound judgment, and ability to manage multiple tight and conflicting deadlines
Ability to work independently and as part of a team
Knowledge of CDISC, SDMT, CDASH, GCP and other regulatory requirements for global clinical trials
Knowledge of collaborative functions and activities of global clinical trials
Some travel (20%) may be required, potentially over weekends
Strong communication, collaboration, adaptability, ethical behavior, resilience, and commitment to continuous learning

Benefits

Comp & perks

Annual performance-based bonuses
Equity-based incentive program
Generous vacation
Paid wellness days
Support for learning and development
Hybrid and remote work arrangements are available at Telix
Equal opportunity employment