Global Study Associate - Oncology (6 Month Secondment/fixed-term)

Workatwamz

Not specified (assumed remote or hybrid based on role nature).
Electronic trial master file (etmf) management
Clinical trial regulations (ich gcp)
Astrazeneca standard operating procedures (az sops)
The Global Study Associate position at Workatwamz focuses on supporting clinical studies in Late Development Oncology. The role involves collaboration with various teams to ensure compliance with clinical trial regulations and efficient study execution

Job Summary

  • The GSA supports Global Study Director (GSD) / Global Study Associate Director (GSAD) and Global Study Managers (GSMs) in delegated aspects of clinical study execution in accordance with the Study Team Operating Model (STOM), AZ Project Management Framework, current clinical trial regulations (e.g. ICH GCP), AstraZeneca Standard Operating Procedures (AZ SOPs), AZ policies and best practices (e.g. AZ guidelines) and in line with AZ values and behaviours.
  • Responsibilities include initiating and leading the set-up, maintenance, and closure of the electronic Trial Master File (eTMF) to ensure compliance, interacting with internal staff and external vendors for document collection, and contributing to electronic applications/submissions.
  • AstraZeneca embraces diversity and equality of opportunity and is committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.

Matching Summary

Match Score: 75

The Global Study Associate position at Workatwamz focuses on supporting clinical studies in Late Development Oncology. The role involves collaboration with various teams to ensure compliance with clinical trial regulations and efficient study execution.

Skills & Requirements

Must-have

  • electronic Trial Master File (eTMF) management
  • clinical trial regulations (ICH GCP)
  • AstraZeneca Standard Operating Procedures (AZ SOPs)
  • tracking and communication tools
  • administrative tasks and logistic support

Nice-to-have

  • embraces diversity and equality
  • inclusive and diverse team
  • harnessing industry-leading skills
  • work independently and in a team

Key Requirements

  • Education in medical or biological sciences
  • Proven organizational and analytical skills
  • Previous administrative training/experience
  • Computer proficiency in day-to-day tasks
  • Working knowledge of Clinical Study Process and ICH/GCP
  • Excellent verbal and written communication in English
  • Ability to prepare presentation materials

Work Rights

Not specified

Tailored Resume

Cover Letter