Address
Form of workResponsibilities:
- 7+ years data management experience and B.S./B.A. in a science or technical discipline degree.
- Previous CRO experience is strongly recommended.
- Proficient in MS Excel.
- Ability to program in SQL or SAS desirable, but not required.
- Experience with various data collection and Electronic Data Capture (EDC) systems and related tools and processes. Medidata Rave EDC, Medrio e Clinical and Clario EDC experience.
- Excellent oral and written communication skills.
- Ability to work in a collaborative and multi-disciplinary environment.
- Attention to detail, ability to prioritize and manage multiple projects with competing and aggressive timelines.
- Availability to travel for clinical team meetings and/or Investigator Meetings if needed.
- Good knowledge of Food and Drug Administration (FDA), Europe Medicines Association (EMA), International Conference on.
- Harmonization (ICH) guidelines and Good Clinical Practices (GCPs) including regulatory requirements for the conduct of clinical development programs, especially as related to data handling and processing.
