Description
This ideal candidate will have:- Experience managing and overseeing all processes of involved in a global clinical trial including but not limited to: IRB submissions, assisting in creating study timelines, budgets, CRFs, study documents (ICFs, protocols, study instructions), maintaning TMF and study data, working with outside vendors and CROs, site and PI selection.
- Experience managing Phase II and Phase III clinical trials.
- Experience in Oncology research is a must.
- Previous monitoring experience is a must.
- Previos CRO experience is a plus.
- This position requires a minimum of at least 5 years of previous experience in clinical research
- Must be willing to travel (at least 25% domestically with the possibility of some international travel).
This job is located inMountain View,CA. There is no option to work remotely.
This is an immediate hire position. We are currently conducting phone interviews.
If this position seems like a good fit for your career goals and skill set, please send me an updated resume. If this is not exactly what you are looking for, but are interested in other positions within the pharmaceutical space, please reach out to me as I specialize in placing candidates within this industry.
If you have a colleague who you think would be a good fit for this position, please feel free to forward this message along.
To find out more about Real Staffing please visit www.realstaffing.com