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Clinical Data Analyst

Katalyst CRO

Role overview

Qualifications

  • Bachelor's or Master's degree in a relevant field or equivalent experience
  • 7+ years of clinical data programming experience, with a minimum of 5 years in oncology
  • Hands-on experience across Phase I, II, and III oncology trials
  • Proficiency in SAS; working knowledge of Medidata Rave, Business Objects, and Crystal Reports

Responsibilities

  • Develop, maintain, and execute SAS programs to support external data transfers, including validation against vendor transfer specifications
  • Generate and maintain Data Review Listings (DRLs) and Study Health Metrics (SHMs) in accordance with study timelines
  • Perform peer review of DRLs and data reconciliation reports
  • Monitor automated job logs and resolve issues as needed

Key facts

Hard skills

Other skills

  • Collaboration
  • Problem Solving

About the company

Katalyst CRO logo

Katalyst CRO

Contract Research Organizations (CRO)

Katalyst CRO | Advancing Healthcare & Life Sciences with Expert Research & Regulatory Solutions Katalyst Healthcare & Life Sciences (Katalyst CRO) is a Global Contract Research and Knowledge Process Outsourcing Organization (CRO) dedicated to driving innovation in research, regulatory compliance, and quality excellence for pharmaceutical, biotechnology, and medical device companies worldwide. With a strong foundation in cGxP & ICH-GCP-compliant clinical research, we offer fully customizable, end-to-end solutions, covering everything from pre-clinical studies to Phase I–IV clinical trials, regulatory affairs, and validation services—ensuring seamless drug and device development. Our Expertise Across the Product Lifecycle: 🔹 Pre-Clinical Research & Development – In-Vitro (Lab-Based) & In-Vivo (Animal) Studies 🔹 Clinical Research & Development – Trial Management, Data Management, Biostatistics, Medical Writing, Pharmacovigilance 🔹 Regulatory & Quality Compliance – cGxP (GMP, GLP, GCP) Validations, Regulatory Affairs, Process & System Validations 🔹 Strategic Human Resourcing – Connecting top-tier talent to life sciences and healthcare organizations With deep industry expertise and a flexible, client-centric approach, Katalyst CRO leverages an advise-build-operate model to de-risk and accelerate research programs. We help organizations achieve regulatory success, optimize quality systems, and bring life-changing therapies to market faster—ultimately improving global patient health and safety. 💡 Partner with Katalyst CRO to bring breakthrough therapies to market with confidence. 📩 Let’s connect and shape the future of healthcare together!

Company details

IndustryContract Research Organizations (CRO)
Company size51 - 200

Links

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Job description

Key Responsibilities:
  • Develop, maintain, and execute SAS programs to support external data transfers, including validation against vendor transfer specifications
  • Generate and maintain Data Review Listings (DRLs) and Study Health Metrics (SHMs) in accordance with study timelines
  • Perform peer review of DRLs and data reconciliation reports
  • Monitor automated job logs and resolve issues as needed
  • Retrieve and post external vendor data using sFTP/FTP clients and vendor portals
  • Collaborate with data managers, statistical programmers, biostatistics, and clinical operations to support data cleaning and integrity activities
  • Contribute to the development and maintenance of SAS macro programs and departmental programming standards
  • Participate in SOP and work instruction development, including program validation and documentation
  • Provide guidance and support to junior members of the data programming team

Qualifications:

  • Bachelor's or Master's degree in a relevant field or equivalent experience
  • 7+ years of clinical data programming experience, with a minimum of 5 years in oncology
  • Hands-on experience across Phase I, II, and III oncology trials
  • Proficiency in SAS; working knowledge of Medidata Rave, Business Objects, and Crystal Reports
  • Familiarity with CDISC, 21 CFR Part 11, ICH, and GCP guidelines
  • Experience with sFTP/FTP tools and vendor data portals

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MR

Marcus Rivera

Chief Revenue Officer

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