eCOA Screen Review Specialist at IQVIA

Madrid, Community of Madrid, Spain

IQVIA Logo
Not SpecifiedCompensation
Junior (1 to 2 years)Experience Level
Full TimeJob Type
UnknownVisa
Clinical Research, PharmaceuticalsIndustries

Requirements

  • High school diploma or equivalent (Bachelor's degree preferred)
  • Excellent written/verbal communication skills
  • Fluency in English (essential); additional language is a strong asset
  • Any previous experience in project management of localization and/or quality assurance work (bonus)
  • Meticulous attention to detail to ensure accuracy and consistency in translated content and project documentation
  • Ability to follow instructions/guidelines, work independently and on own initiative
  • Ability to establish and maintain effective working relationships with co-workers, managers, and clients with demonstrated cultural and emotional intelligence
  • Keen eye for detail, excellent analytical and problem-solving skills

Responsibilities

  • Conduct detailed reviews of eCOA screens to ensure accuracy, functionality, and compliance with study protocols and regulatory standards
  • Verify the correctness of translated content on eCOA screens, ensuring linguistic accuracy and cultural appropriateness
  • Test the functionality of eCOA screens, including navigation, data capture, and response logic, to ensure they work as intended (if applicable)
  • Implement quality assurance procedures to identify and rectify any issues related to screen content, layout, and functionality
  • Work closely with project managers, linguists, developers, and other stakeholders to address and resolve any discrepancies or issues found during the review process
  • Document review findings, test results, and any changes made to eCOA screens, maintaining thorough and accurate records
  • Ensure that all screen review activities comply with relevant regulatory requirements and industry standards for clinical research and eCOA implementation
  • Manage multiple, parallel projects simultaneously
  • Follow company and department standard operating procedures
  • Assist with the establishment of new procedures and offer suggestions for process improvements for existing procedures
  • Work with Project Managers and Team Leads to contribute to the continuous improvement of processes and develop relevant guidance documents

Skills

eCOA
Screen Review
Quality Assurance
Localization
Translation Verification
Linguistic Accuracy
Regulatory Compliance
Project Management
Clinical Protocols
SOPs

IQVIA

Advanced analytics and clinical research services

About IQVIA

IQVIA provides advanced analytics, technology solutions, and clinical research services specifically for the life sciences industry. Their services utilize extensive data resources and technology to create connections within healthcare, allowing clients to gain insights that help speed up the development and marketing of new medical treatments. This process is facilitated by their IQVIA Connected Intelligence™ system, which offers quick and flexible insights. IQVIA stands out from competitors by focusing on patient privacy, employing various technologies to protect individual data. The company's goal is to enhance healthcare outcomes by supporting biotech, pharmaceutical, and medical device companies, as well as researchers and government agencies, in understanding diseases and advancing medical science.

Durham, North CarolinaHeadquarters
1998Year Founded
$3,526MTotal Funding
POST_IPO_EQUITYCompany Stage
Cybersecurity, Biotechnology, HealthcareIndustries
10,001+Employees

Risks

Rapid advancement of cancer vaccines may disrupt traditional clinical research models.
Proliferation of disparate technological solutions causes technology overload in clinical trials.
Generative AI technologies face challenges in adoption due to data privacy concerns.

Differentiation

IQVIA leverages advanced analytics and big data for life sciences solutions.
The company offers privacy-enhancing technologies to protect individual patient data.
IQVIA's AI Assistant provides rapid, actionable insights for healthcare and life sciences.

Upsides

Increased adoption of decentralized clinical trials enhances patient-centric study designs.
AI-driven drug discovery accelerates identification of potential drug candidates.
Expansion of telemedicine facilitates remote patient monitoring and data collection.

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