> Markdown version of [/jobs/ext/4158427-data-coordinator-qc-reviewer](https://www.wearedevelopers.com/jobs/ext/4158427-data-coordinator-qc-reviewer). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Data Coordinator & QC Reviewer - **Company:** Pharmaron, Inc. - **Location:** Exton, PA, United States - **Experience:** Experienced - **Salary:** $65,000.0 - $70,000.0 - **Contract:** Permanent contract - **Skills:** Microsoft Excel, Data Transmissions, Data Systems, Document Management Systems, Laboratory Information Management Systems, Microsoft Office, Google Cloud, Data Delivery - **Published:** October 25, 2026 - **Apply:** https://www.indeed.com/viewjob?jk=92b633e4d5e23d15 ## About the Role Pharmaron is seeking a detail-oriented Data CoordinatorQC Reviewer to support the review, organization, quality control, and delivery of scientific data generated in a regulated laboratory environment. This role plays a critical part in ensuring data accuracy, regulatory compliance, and timely delivery of study results to our pharmaceutical and biotechnology clients., * Bachelor's degree in a Life Science or related field. * Minimum 2 years of experience in a regulated laboratory, CRO, pharmaceutical, or clinical research environment. * Working knowledge of GLP, GCP, ICH guidelines, and 21 CFR Part 11. * Strong attention to detail and organizational skills. * Proficiency in Microsoft Office, particularly Excel. * Ability to manage multiple projects and meet competing deadlines. Preferred Qualifications * Experience with laboratory data management, quality review, or scientific document control. * Experience supporting sponsor data transfers and regulatory inspections. * Familiarity with LIMS, eTMF, or other regulated data systems. ## Description * Review, compile, and organize scientific documents and study data in compliance with GLP, GCP, and internal SOPs. * Perform quality control reviews of laboratory data and supporting documentation. * Prepare and coordinate data transfers according to sponsor specifications and timelines. * Generate and manage transfer files including Excel, CSV, PDF, and ZIP formats. * Collaborate with scientists, project managers, QA, and QC teams to ensure accurate and timely data delivery. * Support audit responses, reconciliation activities, and continuous process improvement initiatives. * Track project timelines and communicate data transfer status to stakeholders.