Clinical Support Specialist – Regulatory, Study Start-Up, Site Activation

Jobtailor

Buenos Aires

Presencial

ARS 600.000 - 900.000

Jornada completa

14 días+
Generador de candidaturas

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Supera los filtros ATS

Descripción de la vacante

Jobtailor in Buenos Aires, Argentina is seeking a detail-oriented clinical operations support professional. You will provide operational and administrative support across clinical functions, manage documentation, and ensure study files remain inspection-ready.

Proficiency in MS Office and English communication are essential, with a collaborative, team-driven mindset. The role involves coordinating cross-functional communications, tracking milestones, and leveraging AI-enabled dashboards to

Formación

  • Associate’s degree or equivalent combination of education, training and experience.
  • Minimum 1 year clinical operations experience.
  • Demonstrated understanding of clinical operations.
  • Utilize problem-solving techniques effectively.
  • Strong documentation and communication skills (written and spoken English).
  • Team-oriented approach.
  • Proficiency in Microsoft Office Suite (Outlook, Word, Excel, PowerPoint, Publisher).
  • Ability to embrace new technologies and learn and adopt new technologies and tasks, including AI-enabled tools and dashboards where approved/available.
  • Ability to manage competing priorities in a dynamic fast-paced environment.
  • Demonstrated ability to work independently as well as part of a team.
  • Good organizational skills and attention to detail.
  • Proven ability to take direction from multiple individuals and set priorities accordingly.
  • Quality-driven in all assigned activities.
  • Flexibility and willingness to adapt to a rapidly changing environment and learn/perform new functions.

Responsabilidades

  • Provide operational and administrative support to one or more clinical functions.
  • Coordinate documentation and communications, including maintaining and managing shared mailboxes, organizing project files, tracking action items, and ensuring timely follow-up with cross-functional stakeholders
  • Enter, maintain, and reconcile information in agreed project and clinical tracking systems
  • Track timelines and milestones
  • Perform document management, including document creation, compilation, formatting, version control, and quality control
  • Translate documents using approved vendors/systems
  • Use AI-enabled tools, dashboards, and automated reports to provide logistical, organizational, and analytical support
  • Support Trial Master File (TMF) filing and related document process activities within scope, ensuring inspection-ready documentation
  • Provide quality deliverables and follow project requirements and applicable country rules
  • Review and comply with applicable SOPs and Work Instructions, ensure training compliance, and maintain accurate timesheet reporting
  • Monitor workload/scope, budgeted effort, and project hours; escalated discrepancies in a timely manner
  • Maintain awareness of clinical research by completing necessary and assigned training

Conocimientos

Clinical Operations
Document Management
Project Tracking
Quality Control
Version Control
Training Compliance
Microsoft Office
AI-enabled Tools
Team Collaboration
Problem-Solving

Educación

Associate's Degree

Herramientas

AI-Enabled Tools
Dashboards
Clinical Tracking Systems
Project Management Software
Shared Mailboxes

Descripción del empleo

  • Provide operational and administrative support to one or more clinical functions
  • Coordinate documentation and communications, including maintaining and managing shared mailboxes, organizing project files, tracking action items, and ensuring timely follow-up with cross-functional stakeholders
  • Enter, maintain, and reconcile information in agreed project and clinical tracking systems
  • Track timelines and milestones
  • Perform document management, including document creation, compilation, formatting, version control, and quality control
  • Translate documents using approved vendors/systems
  • Use AI-enabled tools, dashboards, and automated reports to provide logistical, organizational, and analytical support
  • Support Trial Master File (TMF) filing and related document process activities within scope, ensuring inspection-ready documentation
  • Provide quality deliverables and follow project requirements and applicable country rules
  • Review and comply with applicable SOPs and Work Instructions, ensure training compliance, and maintain accurate timesheet reporting
  • Monitor workload/scope, budgeted effort, and project hours; escalated discrepancies in a timely manner
  • Maintain awareness of clinical research by completing necessary and assigned training
Requirements
  • Associate’s degree or equivalent combination of education, training and experience.
  • Minimum 1 year clinical operations experience
  • Demonstrated understanding of clinical operations
  • Utilize problem-solving techniques effectively
  • Strong documentation and communication skills (written and spoken English)
  • Team-oriented approach
  • Proficiency in Microsoft Office Suite (Outlook, Word, Excel, PowerPoint, Publisher)
  • Ability to embrace new technologies and learn and adopt new technologies and tasks, including AI-enabled tools and dashboards where approved/available
  • Ability to manage competing priorities in a dynamic fast-paced environment
  • Demonstrated ability to work independently as well as part of a team
  • Good organizational skills and attention to detail
  • Proven ability to take direction from multiple individuals and set priorities accordingly
  • Quality-driven in all assigned activities
  • Flexibility and willingness to adapt to a rapidly changing environment and learn/perform new functions
Core Competencies

Demonstrates proficiency in clinical operations and project management, with strong skills in documentation, communication, and the use of AI-enabled tools for logistical and analytical support. Capable of managing competing priorities while ensuring quality deliverables and compliance with applicable regulations.

Highest-signal resume keywords
  • Clinical Operations Experience
  • Microsoft Office Suite Proficiency
  • Document Management Skills
  • Problem-Solving Techniques
  • Team-Oriented Approach
ATS Optimization Keywords
Hard Skills
  • Clinical Operations
  • Document Management
  • Project Tracking
  • Quality Control
  • Version Control
  • Timeline Tracking
  • Data Reconciliation
  • Documentation Creation
  • SOP Compliance
  • Training Compliance
Soft Skills
  • Communication Skills
  • Organizational Skills
  • Attention to Detail
  • Flexibility
  • Team Collaboration
Certifications & Qualifications
  • Associate's Degree
Industry Keywords
  • Clinical Research
  • Trial Master File (TMF)
  • Inspection-Ready Documentation
  • Cross-Functional Stakeholders
  • Dynamic Environment
Tools & Technologies
  • AI-Enabled Tools
  • Dashboards
  • Clinical Tracking Systems
  • Project Management Software
  • Shared Mailboxes
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