Biotechnology companies are revolutionary...
How do you feel about leading the Data Management of a Biotech at the forefront of the industry?
You will be responsible for coordinating and executing all actitivies within Data Management, most noticably reviewing protocols, creating CDISC standards for trials and ensuring the readiness of all Data Management deliverables for Regulatory Agency audits.
As a knowledgable member of this growing team, you will perform trial-level oversight and liaise with a variety of clinical functions to establish expectations for dataset content and structure. Good communications skills and effective project/time management will see you thrive in this role.
Longevity is guaranteed with this 12-month contract and it is expected that this will be extended.
If you would like to be a part of this innovative Biotech, please apply below for immediate consideration!