Offer summary
Qualifications:
Bachelor’s/Master’s degree in relevant field., 5+ years experience in pharma/CRO/academic sites., Advanced understanding of clinical trial process., Leadership, problem-solving, time management skills., Fluency in English and international regulations knowledge..
Key responsabilities:
- Translate scientific requirements into technical specifications.
- Collect, curate, standardize clinical trial data.
- Ensure data quality through various checks.
- Support development process with expertise.
- Collaborate internationally for project success.