Senior Data Governance Analyst, MDM/RDM

Reposted 7 Hours Ago
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3 Locations
In-Office or Remote
Senior level
Pharmaceutical
The Role
The Senior Data Governance Analyst manages MDM/RDM processes, ensures data quality, collaborates with stakeholders, and supports governance frameworks.
Summary Generated by Built In

When our values align, there's no limit to what we can achieve.
 
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Job Purpose: 

The Senior Data Governance Analyst, MDM/RDM contributes to the consistent implementation of Parexel’s data governance frameworks and contributes to the development of high-quality, well-managed master and reference data (MDM and RDM). This role focuses on the day-to-day operational management of MDM/RDM processes, issue resolution, collaboration with global data stewards across domains such as Investigator, Site, and Study, and the alignment of master and reference data across Parexel. Operating within the Data Governance Enablement team, this role collaborates closely with data governance leadership, data domain owners, data and technology (D & T), and business stakeholders to enable the accuracy, consistency, and usability of master and reference data.

Key Accountabilities:

Data Management:

  • Contributes to the implementation of the established MDM/RDM roadmap in partnership with data governance leadership, including participation in user acceptance testing (UAT) to validate new or updated master and reference data processes, data models, and system functionality.

  • Perform day-to-day activities for managing master data and reference data across domains.

  • Translate business needs into clear, actionable requirements for D & T development teams.

  • Evaluate data dependencies, downstream impacts, and alignment with architectural and governance standards. Support MDM/RDM curation and lineage.

  • Ensure that master and reference data processes align with policies, business rules, and stewardship expectations.

  • Maintain alignment across MDM/RDM assets, data catalogs, and repositories.

Data Support:

  • Monitor, investigate, and triage issues related to master and reference data quality, escalating when necessary.

  • Collaborate with business and technical teams to solve data issues and identify process improvements.

  • Support enhancements to MDM/RDM workflows, process updates, documentation, and training materials.

  • Provide guidance on best practices for maintenance and change control activities related to MDM/RDM data, processes and governance expectations.

Stakeholder Management & Collaboration:

  • Build strong working relationships with global data stewards, business partners, D & T teams, and data governance peers.

  • Support cross-functional initiatives requiring master or reference data expertise.

  • Maintain a log of MDM/RDM data owners for issue resolution, decision-making, escalation, and communication pathways.

  • Contribute subject-matter expertise related to MDM/RDM practices.

Data Innovation and Compliance:

  • Assist with planning and evaluating future MDM/RDM tools, capabilities, and enhancements.

  • Contribute to the reporting of MDM/RDM metrics, KPIs, and adoption indicators.

  • Ensure alignment with data privacy, data protection, and regulatory considerations relevant to clinical research datasets.

Skills:

  • Strong knowledge of Master Data Management and Reference Data Management principles and processes.

  • Understanding of data governance frameworks, metadata practices, and data lifecycle management.

  • Excellent problem-solving, analytical, and organizational skills.

  • Clear written and verbal communication skills; ability to translate complex data concepts into business-friendly language.

  • Ability to work effectively in a global, matrixed environment and collaborate across cultures and time zones. Strong team-first mindset.

  • Demonstrated professionalism, follow-through, and ability to work independently.

  • Balanced approach to short-term needs and long-term governance expectations.

  • Ability to manage multiple tasks simultaneously and adapt to changing priorities.

Knowledge and Experience:

  • Experience implementing or supporting MDM and RDM capabilities in an enterprise environment.

  • Familiarity with MDM platforms, reference data tools, and enterprise information management practices. Familiarity with Reltio or similar enterprise platform is helpful.

  • Experience contributing to data governance or data analytics initiatives.

  • Experience working with global teams in a matrixed organization.

  • Understanding of data privacy, data protection, and data quality principles.

  • Experience in life sciences, pharmaceutical, or CRO environments beneficial.

Education:

  • Degree in information science, data analytics, information systems, life sciences, or related field preferred.

Top Skills

Data Governance
Mdm
Rdm
Reltio
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The Company
HQ: Durham, North Carolina
20,524 Employees

What We Do

Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com.

Community Guidelines
Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are:

• Abusive, harassing or threatening to others.
• Defamatory, offensive, obscene, vulgar or depicting violence.
• Hateful targeting by race/ethnicity, age, color, creed, religion, gender,
sexual preference or orientation, nationality or political beliefs.
• Sexually explicit or pornographic.
• Fraudulent, deceptive, libelous, misleading or unlawful.
• Referencing criminal or illegal activity.
• Spamming.

We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.

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