Quality Control Specialist

ICON (Accellacare/PRA) US, Portland, OR Updated 30 August 2026
Quality Assurance

Job description

Quality Control Specialist - Portland, Oregon (OR) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. Quality Control Specialist Position Overview The Quality Control Specialist plays a critical role in ensuring the accuracy, integrity, and compliance of laboratory data, documentation, and quality records. This position performs quality control reviews of study-related data and laboratory documentation, supports quality systems and document control processes, monitors laboratory quality metrics, and contributes to continuous improvement initiatives. The ideal candidate is highly detail-oriented, analytical, and committed to maintaining the highest standards of quality and regulatory compliance within a regulated laboratory environment. Position Summary The Quality Control Specialist is responsible for the review, verification, and maintenance of laboratory data, documentation, and quality records in accordance with established Standard Operating Procedures (SOPs), study protocols, analytical methods, and regulatory requirements. This role collaborates cross-functionally to ensure data integrity, compliance, and consistency across laboratory operations while supporting quality systems, laboratory metrics reporting, document control initiatives, and continuous improvement efforts. The Quality Control Specialist contributes to departmental objectives by working independently, managing multiple priorities, completing assigned projects within established timelines, and maintaining effective communication with internal stakeholders. Core Values & Behaviors Recognize, exemplify, and adhere to ICON's values centered on People, Clients, and Performance. Embrace and contribute to a culture of continuous improvement focused on enhancing efficiency, quality, compliance, and customer satisfaction. Demonstrate a strong commitment to quality, accuracy, integrity, and regulatory compliance. Collaborate effectively within a team environment and contribute to departmental and organizational goals. Communicate professionally and effectively with supervisors, colleagues, Project Leaders, Project Managers, and cross-functional teams. Prioritize workload effectively and manage time to meet deadlines. Maintain punctual and reliable attendance in accordance with company policy. Adhere to all safety procedures and maintain a safe working environment. Key Responsibilities Data Review & Compliance Perform quality control (QC) review of study participant results and laboratory run packets to ensure accuracy, completeness, and compliance with applicable SOPs, protocols, and regulatory requirements. Conduct review of Biomarker Reports and supporting study documentation to verify data accuracy and integrity. Perform QC review of validation documentation and associated records. Review methods, reports, study data, and supporting documentation for accuracy, consistency, completeness, and proper formatting. Identify, document, and communicate data discrepancies, quality issues, and compliance concerns in a timely manner. Assist with investigations and resolution of data and documentation discrepancies to support study integrity and quality objectives. Provide backup support for Incoming Materials review activities and QC review of Production Batch Records. Read, understand, and compl

Stand out for this role

NoxPharm tailors your CV to this exact job description — matching the keywords recruiters and ATS systems screen for. Built for pharma & life sciences.

Tailor my CV now — free to try