Clinical Research Associate, CRA

Pfizer

Clinical Research Associate coordinating clinical trial activities to support managers and enhance treatment outcomes. Organizing work and maintaining compliance with protocols and regulations.

Posted 7/16/2026full-timeRemote • 🇦🇷 ArgentinaJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in coordinating clinical trial activities while ensuring compliance with ICH-GCP and SOPs. Proficient in maintaining trial documentation and providing administrative support to project managers within established timelines.

Highest-signal resume keywords

Clinical Trial CoordinationICH-GCP ComplianceMicrosoft Office Suite ProficiencyOrganizational SkillsAttention to Detail

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial Activities CoordinationTrial Master File MaintenanceData Tracking and ManagementProtocol SupportInformed Consent Document Preparation

Soft Skills

Strong Organizational SkillsAbility to Prioritize TasksIntroduction of New Ideas

Tools & Technologies

Corporate Clinical Trial RegistryLocal Tracking Spreadsheets

Industry Keywords

Standard Operating ProceduresRegulatory AuthoritiesEthics CommitteesInspection Readiness

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Coordinate and support clinical trial activities, assisting managers in their execution.
Contribute to project tasks and milestones, organizing work to meet deadlines.
Work in a structured environment using established procedures, seeking guidance from colleagues.
Maintain the Pfizer Trial Master File (PTMF) in compliance with ICH-GCP and SOPs, and ensure team members update tracking and files as needed.
Timely update trial and site information in the Corporate Clinical Trial Registry and support Clinical Trial Applications to ethics committees and regulatory authorities.
Provide administrative support for protocols and Informed Consent Documents (ICD) to global Project Managers and Study Managers, assisting with activities within set timelines.
Develop and maintain local tracking spreadsheets for study-related documents, data, and activities, prepare supportive materials for sites, attend training programs, and identify process improvements for inspection readiness and PTMF compliance.

Requirements

What you’ll need

BA/BS with any years of experience
Demonstrated ability to introduce new ideas and knowledge on all relevant Standard Operating Procedures
Ability to prioritize multiple tasks and develop strategies for the completion of all required activities
Strong organizational skills and attention to detail
Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint)

Benefits

Comp & perks

Health insurance
Flexible work arrangements
Professional development opportunities