Clinical Trial Assistant

Galderma

Boston, United States
Trial master file (tmf) management
Invoice and payment processing
Regulatory document handling
The Clinical Trial Assistant (CTA) is responsible for performing a variety of research, data base and clerical duties of a complex and technical nature in support of multiple clinical trials

Job Summary

  • The Clinical Trial Assistant (CTA) is responsible for performing a variety of research, data base and clerical duties of a complex and technical nature in support of multiple clinical trials.
  • Key responsibilities include Trial Master File (TMF) management, processing invoices, and serving as a liaison for regulatory documents and clinical supplies.
  • Galderma offers an opportunity to work in a diverse and inclusive environment, advancing dermatology for every skin story with a focus on employee growth and impact.

Matching Summary

The Clinical Trial Assistant (CTA) is responsible for performing a variety of research, data base and clerical duties of a complex and technical nature in support of multiple clinical trials.

Skills & Requirements

Must-have

  • Trial Master File (TMF) management
  • Invoice and payment processing
  • Regulatory document handling
  • Liaison with CRO and sites
  • Study set-up activities

Nice-to-have

  • Positive energy and collaboration
  • Passion for dermatology
  • Embrace diversity and inclusion
  • Proactive and flexible attitude

Key Requirements

  • 3+ years of clinical administrative or regulatory experience
  • 1+ year of Clinical Trial Assistant experience
  • Knowledge of FDA GCP-ICH Guidelines
  • Bachelor's Degree or equivalent experience

Work Rights

Not specified

Tailored Resume

Cover Letter