Clinical Data Governance Lead

Centraprise

New Jersey

On-site

USD 110,000 - 150,000

Part time

14 days+
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Job summary

Centraprise is seeking a Clinical Data Governance Lead in New Jersey to assist with data governance initiatives crucial for clinical development. The ideal candidate will have a strong background in the clinical trial lifecycle and data management.

Key responsibilities include leading discussions with senior leaders, preparing presentations, and managing business glossaries, data catalogs, and data quality protocols. Strong communication and stakeholder engagement skills are essential for this role.

Qualifications

  • Strong pharmaceutical and clinical background with understanding of clinical trial processes.
  • Deep understanding of clinical trial data lifecycle and data management.
  • Ability to lead governance discussions and facilitate workshops.

Responsibilities

  • Assist with data governance initiatives including business glossaries and data catalogs.
  • Prepare and present high-quality presentations.
  • Influence senior-level leaders and drive consensus on definitions.

Skills

Clinical trial processes
Data governance methodologies
Stakeholder engagement
Written and oral communication

Job description

Job Title : Clinical Data Governance Lead

Employment Type : Contract

Location: New Jersey (Onsite)

Job Description :

Summary

Experienced, senior-level individual with strong experience in clinical development (clinical study lifecycle and clinical data lifecycle) required to assist with data governance initiatives, including business glossaries, data catalogs, metadata management, data lineage, master and reference data management, data quality, data policies, data controls, data sharing, data stewardship, etc.

Requires strong oral and written communication, expertise in analyzing clinical processes and data, experience meeting with and influencing senior-level leaders at all levels, adept at preparing and presenting high-quality presentations and leading workshops, and being a proactive, self-driven team player.

Qualifications – Required
  • Strong pharmaceutical and clinical background with deep understanding of clinical trial processes, study lifecycle, and regulated data environments.
  • Deep understanding of clinical trial data lifecycle, data types, data usage, data management, related roles and responsibilities.
  • Strong communication and stakeholder engagement skills, with the ability to explain data governance methodologies, standards, and business value to both technical and non-technical audiences.
  • Ability to lead and influence governance discussions by facilitating workshops, gathering requirements, driving consensus on definitions and standards, and supporting adoption of governed clinical data assets across the organization.
  • Very strong written and oral communication skills.
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