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Online Resumes with "Regional CRA"



Regional CRA, Phoenix

I would like to join a company with a global footprint that values its employees as individuals as well as for the work they perform. The right company for me will utilize my current capabilities while allowing for the expansion of my knowledge and skills, and will encourage my desire to grow into roles of increasing responsibility. I believe that a successful company is one that truly values its human resource.

Tags for this Online Resume: Monitor, Project Manager, CRA, Clinical Research, Study Manger

Talented Clinical Research Associate

Seeking CRA position or pathway to home-based, regional CRA position. I strive to master my projects and enjoy a collaborative environment with bright, hard-working individuals.

Research Regulatory Coordinator

I would like to continue my career in the regulatory field, such as Assistant Director of Regulatory Affairs or entry level regional CRA or managerial position.

Tags for this Online Resume: regulatory, coordinator, research, quality assurance, CRA, homebased

Clinical Regional Monitoring - 34 Years of Experience - Near 07076

SUMMARY An experienced Senior Clinical Research Associate with considerable Local, Regional, and US experience within the CRO environment. Key experiences are within Endocrinology, Neurology, Cardiovascular, Infectious Disease, Bone, and Oncology. * EXPERIENCE * PRA Health Sciences August 2016 - October 2017 * Job Title: Sr. Clinical Research Associate * A member of a CRO team dedicated to a major sponsor program to evaluat...

Tags for this Online Resume: Clinical Research, Research, Billing, Cancer, Query, Documentation, Oncology, Team Lead, Cardiovascular, Management

Featured Profile

Clinical Research

I am currently exploring new opportunities where I can utilize my more than 20 years of experience to add value to the clinical research industry. My experience includes 8.5 years as a Clinical Trial Assistant, 4 years as an In-House CRA, 1.5 years as a Regional CRA, and 5 years supporting study start-up and site activation. I enjoyed managing regional clinical sites the most and want to further my career and skills in this...

Tags for this Online Resume: Protocol, Management, Documentation, Data Entry, Clinical Research, Compliance, Document Review, Research, Query resolution, Inform Consent Form, eCRF guidelines, SAE Reporting, AE Reporting, IRB Submissions, Regulatory Compliance, ICH / GCP / FDA guidelines, Database lock timelines met, Site deficiencies resloved, Patient enrollment and retention, Ongoing site education and support, Ensure lines of communication remain open, Study specific SOPs, Electronic Data Capture, InForm, Phase Forward, Medidata, BioClinica, Oracle, Siebel, Share Vault, Phlex Global, PhlexEview, Egnyte, Trial Interactive, Microsoft Word, Excel, Publisher, PowerPoint, DocuSign

Clinical In-house Monitoring - 17 Years of Experience - Near 08844

10+ years of proficient experience into clinical research as a Clinical research associate in pharmaceutical industries and clinical research organizations. * In-house and regional monitoring experience in Phase I, II, & III. * Capable to work as both in-house CRA and as a Regional CRA with efficiency to monitor and manage any number of sites depending on Sponsor's SOP. * Good working knowledge of GCP and ICH guidelines. (...

Tags for this Online Resume: Research, Clinical Research, Management, Quality, Quality Assurance, Quality Control, Audit, Oracle, Filing, Good Clinical Practices