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Principal Clinical Data Engineer

Role overview

Qualifications

  • Bachelor's degree (or equivalent) in a relevant science discipline
  • Advanced proficiency in SQL, SAS, or R
  • Comprehensive knowledge of SOPs, Guidelines, and ICH-GCP
  • Strong experience with clinical data systems

Responsibilities

  • Manage Projects and implement Data Receipt Agreements with vendors
  • Design and implement reconciliation checks for data transfer
  • Review data outputs and provide strategic insights
  • Act as SME and technology owner for data management platforms

About the company

Parexel logo

Parexel

Pharmaceuticals

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.

Company details

Company typeXLarge
IndustryPharmaceuticals
Company size10001

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Job description

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.

Parexel is seeking an experienced Principal Clinical Data Engineer to join our Global Data Operations team. This is a leadership position where you will be recognized as a subject matter expert, providing technical support and strategic guidance to internal and external sponsors while leading high-impact clinical data projects.

As Principal Clinical Data Engineer, you will take the lead on complex projects, liaise with sponsors, Data Management Leads, and cross-functional teams, while maintaining account oversight responsibilities. You will be instrumental in aggregating data from multiple sources and devices, managing external data, and driving operational efficiencies through the development of standards, libraries, and reusable tools.

Key Responsibilities:

Manage Projects & Technology

  • Lead and implement Data Receipt Agreements with vendors in collaboration with cross-functional teams

  • Program and establish import procedures for data ingestion using SAS or alternative technologies (e.g., Workbench)

  • Design and implement reconciliation checks to ensure accurate data transfer

  • Program offline listings and custom reports to provide valuable insights on external data

  • Aggregate data across all sources and manage data structures, missing values, and programming errors

  • Review data outputs and provide strategic insights to study teams and clients

  • Ensure first-time quality on all deliverables

  • Negotiate electronic data timelines and ensure adherence through active project management

  • Monitor project resourcing, identify scope changes, and resolve technical issues

  • Coordinate and lead programming teams to successful project completion within timelines and budget

  • Manage deployment of data management technology for offline listing creation

  • Act as SME and technology owner for data management offline listing platforms

Documentation & Compliance

  • Maintain comprehensive supporting documentation in accordance with SOPs, Guidelines, and Work Instructions

  • Ensure traceability and regulatory compliance across all study activities

  • Document deviations and communicate them to project teams

Support Initiatives & Continuous Improvement

  • Participate in creating standards through tools (SAS macros), libraries, and processes

  • Develop and implement project-specific tools and improvements

  • Lead or drive global initiatives related to processes and new technologies

  • Mentor staff and provide relevant training

  • Assist project teams in problem resolution and technical support

  • Maintain and expand regulatory knowledge within the clinical research industry

Account Leadership & Business Development

  • Serve as point of contact for clients and internal stakeholders on electronic data matters

  • Participate in bid defense meetings

  • Independently contribute ideas on technology and data engineering to support business development

Required Skills & Experience:

  • Bachelor's degree (or equivalent) in a relevant science discipline is preferred, or equivalent work experience

  • Programming Proficiency: Advanced proficiency in at least one of the following: SQL, SAS, or R

  • Regulatory Knowledge: Comprehensive knowledge of SOPs, Guidelines, Work Instructions, System Life Cycle methodologies, ICH-GCP, and applicable regulations (e.g., 21 CFR Part 11) with proven practical application

  • Clinical Data Systems: Strong experience working with at least two systems used to aggregate data in the clinical trial process (e.g., SAS, Workbench, Elluminate)

  • Excellent interpersonal, oral, and written communication skills with concise, audience-tailored messaging and diplomatic approach

  • Highly developed problem-solving capabilities, root cause analysis skills, and ability to make decisions in ambiguous situations

  • Excellent analytical and technical capabilities

  • Written and oral fluency in English

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MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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