Bristol Myers Squibb
ClinicalResearchAssociate
“Clinical Research Associate at Bristol Myers Squibb. Skills: clinical trial sites, protocol, Standard Operating Procedures (SOPs), ICH Guideline for Good Clinical Practice (GCP), regulatory requirements. study startup at site. overseeing the quality, integrity and compliance of clinical trial sites in accordance with the protocol, Standard Operating Procedures (SOPs), International Council for Harmonization (ICH) Guideline for Good Clinical Practice (GCP), and applicable regulatory requirements”
Industry & Context.
ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function
What They're Looking For.
Must Have
protocol, Standard Operating Procedures (SOPs), International Council for Harmonization (ICH) Guideline for Good Clinical Practice (GCP), applicable regulatory requirements
Nice to Have
Epic, Cerner, Meditech, Allscripts, McKesson, athenahealth, PACS, LIS, RIS, HIPAA, HITECH, FDA (21 CFR), CMS, JCAHO/TJC, DEA, state licensure boards, RN, LPN/LVN, NP, PA, MD/DO, PharmD, RT, PT, OT, LCSW, PsyD, BLS, ACLS, PALS, NRP, CCRN, CEN, CNOR, CRNA, ICU, ED, OR, NICU, Oncology, Cardiology, Neurology, FDA approval process, GxP, ISO 13485, clinical trials (ICH E6 GCP), IND/NDA
What You'll Do.
study startup at site
overseeing the quality
integrity and compliance of clinical trial sites in accordance with the protocol
Standard Operating Procedures (SOPs)
International Council for Harmonization (ICH) Guideline for Good Clinical Practice (GCP)
and applicable regulatory requirements
How You'll Work.
Team & Collaboration
primary point of contact at the site level for both internal and external stakeholders
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