Data Coordinator & QC Reviewer
Pharmaron
Summary
Pharmaron is seeking a detail-oriented Data Coordinator & QC 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.
Job description
Key Responsibilities
- 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.
What We're Looking For
- 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.
Requirements
- 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
Benefits
- Medical, Dental & Vision
- 401(k) Matching
- Paid Time Off
- Paid Sick Leave
- Company Holidays
- HSA Contributions
- FSA Accounts
- Life Insurance
- AD&D Insurance
- Short & Long-Term Disability
- Employee Assistance Program
- Fertility Support
- Maternity Resources
- Professional Development
Company overview
Pharmaron is a premier global life sciences service provider founded in 2004, offering comprehensive research, development, and manufacturing services throughout the entire drug discovery and development process. As a leading Contract Research Organization (CRO) and Contract Development and Manufacturing Organization (CDMO), Pharmaron provides integrated solutions across multiple therapeutic modalities including small molecules, biologics, and cell and gene therapy (CGT) products. The company's extensive service portfolio encompasses synthetic and medicinal chemistry, biology services, DMPK (drug metabolism and pharmacokinetics), pharmacology, toxicology, radiochemistry, CMC (chemistry, manufacturing, and controls), and clinical development services. With over 10,000 employees worldwide and facilities across China, the United States, and Europe, Pharmaron supports pharmaceutical and biotechnology companies in accelerating their R&D programs from early discovery through commercial manufacturing. The company is publicly listed on both the Shenzhen and Hong Kong stock exchanges and maintains a strong commitment to scientific excellence, regulatory compliance, and technological innovation in the life sciences sector.