Clinical Trial Associate

Octapharma AG

Lachen, Switzerland
On-site
Trial master file maintenance
Investigator site file maintenance
Clinical trial documentation preparation
Octapharma AG is seeking a Clinical Trial Associate to support their Clinical Research and Development team in Lachen, Switzerland. The ideal candidate will have experience in clinical trials, particularly in international settings, and will assist with the preparation and maintenance of trial documentation while contributing to a collaborative environment that values family-oriented culture

Job Summary

  • Become part of a vital chain and contribute to our common goal of making people’s lives better.
  • Your main tasks and responsibilities Set up and maintenance of Trial Master Files and lnvestigator Site Files according to Octapharma SOPs.
  • We live diversity and stand for equal opportunities as an employer!

Matching Summary

Match Score: 85

Octapharma AG is seeking a Clinical Trial Associate to support their Clinical Research and Development team in Lachen, Switzerland. The ideal candidate will have experience in clinical trials, particularly in international settings, and will assist with the preparation and maintenance of trial documentation while contributing to a collaborative environment that values family-oriented culture.

Skills & Requirements

Must-have

  • Trial Master File maintenance
  • Investigator Site File maintenance
  • Clinical trial documentation preparation
  • Regulatory package assembly
  • Fluent in English

Nice-to-have

  • Positive attitude
  • Attention to details
  • Team player
  • Independent work
  • Flexible attitude

Key Requirements

  • Previous CTA experience in international trials
  • Office management of international trials
  • Proficient in Word, Excel and Powerpoint
  • Able to prioritize workload within timelines

Work Rights

Not specified

Tailored Resume

Cover Letter