Remote Clinical Data Manager - Global Trials & Data Quality

Telix Pharmaceuticals Limited; Northern (KY); Hybrid; USD 90,000 - 130,000; Full time

Job summary

Telix Pharmaceuticals Limited is seeking a Clinical Data Manager to ensure the integrity, accuracy, and regulatory compliance of clinical trial data. You will support the international roll‑out of our prostate cancer imaging agent and help advance late-stage products in oncology and rare diseases.

In this role you will lead data management activities, oversee EDC builds and data transfers, and collaborate with external vendors while ensuring adherence to CDISC and GCP standards.

Qualifications

• Bachelor’s degree in Health Information Management, Life Sciences or equivalent; advanced degree preferred.
• 3+ years of clinical trial data management experience; leadership of data management activities for complex global trials.
• Experience with CDISC, SDMT, CDASH and GCP regulatory requirements.
• Demonstrated ability to oversee vendors and meet strict timelines.

Responsibilities

• Act as the primary data management SME for assigned Telix clinical trials.
• Oversee EDC build, Data Management Plan, and eCRF completion guidelines.
• Lead data entry, cleaning, and data transfer activities.
• Ensure completeness of data management documentation for eTMF.
• Coordinate with external vendors and support audits and inspections.
• Ensure compliance with CDISC standards and GCP across trials.

Skills

Data management

Vendor management

Regulatory knowledge

Attention to detail

Strong communication

Team collaboration

Project management

Education

Bachelor’s degree in Health Information Management, Life Sciences or equivalent

Tools

EDC systems

eCRF

UAT/test scripts

Job description

Telix Pharmaceuticals Limited is seeking a Clinical Data Manager to ensure the integrity, accuracy, and regulatory compliance of clinical trial data. You will support the international roll‑out of our prostate cancer imaging agent and help advance late-stage products in oncology and rare diseases.

In this role you will lead data management activities, oversee EDC builds and data transfers, and collaborate with external vendors while ensuring adherence to CDISC and GCP standards.