Description
Responsibilities:The Sr.CRA will support the operational management and oversight of aspects of two clinical development programs. The Sr.CRA will work closely with the Clinical Trial Managers, Medical Monitor, Drug Safety, Clinical Data Management, Regulatory/QA, as well as other cross-functional team members/clinical CRO and staff to ensure successful completion of all clinical activities/project deliverables within the required time frame and budget. This is an in-house position.
Requirements:
Cardiovascular, hematology and/or oncology (Phase I - 3) study experience preferred
- Minimum of 3-4 years relevant work experience of which ~ 1.5 years of site monitoring experience
- Experience in the pharmaceutical industry and working knowledge of GCP/ICH guidelines and the clinical development process.
- Advanced MS Excel skills a plus
- BS/RN degree or equivalent
To find out more about Real please visit www.realstaffing.com