Klinischer Monitor - 5 -6 days travel per month

Role Description

This is a full-time remote role for a Clinical Research Associate working sponsor dedicated. The successful candidate will be responsible for overseeing and coordinating clinical trials in compliance with regulatory requirements, and ensuring that all documentation is accurate and complete. The Clinical Research Associate will work closely with a team of clinical research professionals to facilitate the success of the clinical trials.

Qualifications

• Bachelor's degree in a relevant field, such as Life Sciences, Nursing, or other Science-related degree
• At least 1-2 years of experience in Clinical Research, ideally in a Pharma/Biotech setting
• Knowledge of ICH/GCP and FDA regulations, as well as experience with protocol development and study start-up
• Excellent organizational and communication skills
• Proven ability to work independently as well as part of a team
• Proficiency in Microsoft Office, including Word, Excel, and PowerPoint
• Experience with clinical trial software, such as EDC and IWRS, is a plus
• Experience with oncology or specific therapeutic areas is a plus
• Excellent problem-solving and decision-making skills

++please send your cv to application@fleming-research.co.uk++