Clinical Trial Data Specialist

Great Opportunity for a Clinical Trial Data Specialist

Bioforum is a leading Israeli Clinical Research Organization (CRO) providing, among other services, clinical data management services to local life science companies. We are looking for an individual with familiarity with clinical trial data (demographics, medical history, adverse events, labs etc.) to perform part time data Quality Control (QC) activities for one of our largest customers in Israel.

As part of the work the individual will become an expert in CDISC which is the new clinical data standard for submitting New Drug Applications to regulatory authorities.

Hours are flexible. Work can be done from home.

Required skills -

1. At least 2 years experience working with clinical data.

2. At least 2 years experience with Programming (for software QA purposes)

3. Preference for SAS programming experience.

If you are interested and have the required skills, please send your CV to bioforumrec@gmail.com.