Clinical Data Configuration & QC Specialist II

ICON Clinical Research

Ciudad de México

Hybrid

MXN 350,000 - 550,000

Full time

8 days ago

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Benefits offered by this job

Health insurance

Annual leave

Retirement planning

Employee assistance program

Life insurance

Country-specific benefits

Job summary

ICON is a global healthcare intelligence and clinical research organisation seeking an experienced Configuration & QC Specialist II in CDMX. You will design and analyze clinical trials, interpret complex medical data, and help advance innovative treatments.

You will configure and maintain clinical trial databases and EDC systems (Medidata Rave, Oracle Clinical, Inform), perform QC checks, collaborate with data management and statistics teams, and coach junior staff on best practices and

Qualifications

Bachelor's degree in a relevant scientific discipline or healthcare-related field.
3+ years of experience in clinical data management, data validation, or related role, preferably within the pharmaceutical or biotechnology industry.
Proficiency in clinical trial databases and electronic data capture (EDC) systems, such as Medidata Rave, Oracle Clinical, or Inform.
Strong attention to detail, analytical skills, and problem-solving abilities, with the ability to effectively identify and resolve data-related issues.
Excellent communication and interpersonal skills, with the ability to collaborate effectively with colleagues at all levels of the organization.
Proven ability to work independently and manage multiple priorities in a fast-paced, deadline-driven environment.

Responsibilities

Configuring and maintaining clinical trial databases and EDC systems, ensuring accuracy, functionality, and compliance with regulatory requirements.
Performing comprehensive quality control (QC) checks on clinical trial data and study documentation, identifying discrepancies, inconsistencies, and data entry errors.
Collaborating closely with cross-functional teams including data management, biostatistics, and clinical operations to address QC findings and implement corrective actions.
Leading the development and execution of validation plans and procedures to assess the performance and reliability of EDC systems and data management processes.
Providing training, guidance, and support to junior team members on system configuration, data entry guidelines, and QC processes to promote best practices and continuous improvement.