Global Data Manager: Clinical Trials & Compliance

Jobtailor

New Jersey

On-site

USD 85,000 - 135,000

Full time

14 days+

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Job summary

Jobtailor is seeking a Clinical Data Management professional to help establish data standards and ensure regulatory compliance across trials. The role emphasizes quality reviews, content planning, and strong collaboration with cross-functional teams to meet trial needs.

You will participate in inspections and foster improvements in data processes. The ideal candidate holds a Bachelor's degree in a relevant field and has experience in pharmaceutical data management, CDISC standards, and project

Qualifications

Bachelor's degree required in relevant field.
Clinical data management experience preferred.
Familiarity with CDISC standards (SDTM/CDASH) preferred.
Experience in pharma/CRO data management contexts preferred.
Up to 10% travel may be required.

Responsibilities

Gather and review content and integration requirements for eCFR and data collection tools.
Establish conventions and quality expectations for clinical data.
Set timelines and monitor delivery of DMP milestones.
Review DM documents for quality, content and accuracy.
Plan and track data management deliverables with DML and ensure on-time delivery.
Support clinical working groups to meet DM and TA needs.
Participate in regulatory inspections and internal audits as needed.
Contribute to functional plans ensuring quality and consistency.
Identify lessons learned and share FAQs at trial level.
Engage in process and system improvement initiatives.