Continue in the Clinical Research Field
A high-energy and peak-performing, Senior Clinical Research Associate with 15+ years experience ub field monitoring, Regulatory Affairs, QA, QC looking to obtain a contract or full time monitoring or regulatory position with a pharamaceutical, device or biotech company.Certified CRA- SoCRA; certified Regulatory Affairs Specialist certied by RAPS.
Clinical Research Professional with over 15 years combined hospital and research experience & expertise is seeking new career opportunities conducting clinical trials.
Tags for this Online Resume:
Clinical Project Manager, Clinical Research Manager, Senior Clinical Research Associste, Senior Clinical Research Scientist, Clinical Study Operations Specialist, Site Manager
Tags for this Online Resume:
CLINICAL RESEARCH, TRIAL MANAGEMENT, PROJECT MANAGEMENT
To transition in to the health care position with the homeland security agency
I am looking for a long-term contract opportunity preferably in monitoring in Oncology. I would consider a full-time opportunity as well.
I want to ensure that sites that I monitor are completed accurately according to Code of Federal Regulations and GCP/ICH.
To be involved in clinical research
Tags for this Online Resume:
clinical research associate, clinical team leader, senior clinical research associate, monitoring , FDA regulations, Phase 1- IV studies, site selection to site closeout, maintain GCP ICH compliance, GCP ICH compliance
