36 Clinical Research job openings in the Corona, California area

« Corona job listings index · Biotech, R&D & Science

Job listings, help wanted ads and employment postings (last updated on Tuesday, October 21)

Clinical Research Associate - Monitoring, GCP, FDA Regulations

Monster.com

MA-Boston, CyberCoders Matching Great People with Great Companies Learn more about CyberCoders Apply Clinical Research Associate Boston, MA Full-Time $70,000 - $120,000 Apply Apply Clinical Research Associate Boston, MA Full-Time $70,000 - $120,000 Apply Job Details Work out of your home office as a Clinical Research Associate. You will be traveling throughout a localized territory. You can be located anywhe … MORE INFO

Research Associate II

Monster.com

CA-San Diego, Position Overview: This role is primarily to support R&D particle chemistry activities. The position requires provision of high quality latex reagents to R&D scientists and manufacturing personnel engaged in the development and /or improvement of T1, T2 and T3 Triage product lines. Organization Chart: This role reports to the Manager/Principle Scientist responsible for overseeing laboratory activi … MORE INFO

Regional Supervisor

Monster.com

CA-Irvine, Position Summary: Proove Biosciences, Inc. is seeking team players for Regional Supervisorto join a fast growing team supporting physician clinics across the nation. Proove Biosciences is the Personalized Pain Medicine Company. Our mission is to Change the Future of Medicine. With offices in Irvine, California and Annapolis-Junction, Maryland, Proove provides physicians with information to improve … MORE INFO

Research Associate Job

Monster.com

CA-South San Francisco, Company: Yoh Senior Research Associate needed for a contract opportunity with Yoh's client located in South San Francisco, CA. Top Skills Should You Possess: - Cell based assays - qPCR What You'll Be Doing: - Seeking an experienced individual for a Research Associate/Sr Research Associate within the Biochemical and Cellular Pharmacology group. - The successful candidate will be responsible for sup … MORE INFO

Clinical Outsourcing Consultant Job

Monster.com

NJ-Woodcliff Lake, Company: Yoh Clinical Outsourcing Manager needed for a contract opportunity with Yoh's client located in Woodcliff Lake, NJ. What You'll Be Doing: - Support internal customers in the development of outsourcing requirements for Phase I-IV global clinical trials. - Lead and support the qualification and evaluation process for new service providers. - Lead the process of Request for Proposal (RFP) de … MORE INFO

Research Associate Job

Monster.com

DE-Newark, Company: Yoh Research Associate needed for a contract opportunity with Yoh's client located in Newark, DE What you'll be doing: - Treat seeds - Test treated seeds for handling attributes applying standardized protocols. - Package treated seeds for field trial distribution - Execute seed treatment experiments collaboratively with Principal Investigator to generate process data and supply laboratory … MORE INFO

Research Assistant

Monster.com

NC-Cary, Position Summary: Proove Biosciences, Inc. is seeking team players for Research Assistantsto join a fast growing team supporting physician clinics across the nation. Proove Biosciences is the Personalized Pain Medicine Company. Our mission is to Change the Future of Medicine. With offices in Irvine, California and Annapolis-Junction, Maryland, Proove provides physicians with information to improve … MORE INFO

SAS Programmer II

Monster.com

NJ-Bridgewater, Job Number: 424041 SAS Programmer II OVERVIEW Provide statistical programming expertise in SAS for the production of analyses, tabulations, graphics, and listings from clinical trial data. Key responsibilities and skills include, but are not limited to, the following: Contribute to the preparation of analysis plans. Prepare, document and test required programs and procedure data displays in an eff … MORE INFO

Global Training Administrator - Clinical Research

Monster.com

TX-Houston, If you’re interested in working for a Leading, Mid-Size Contract Research Organization (CRO) that has a massive global reach, then look no further, because Pharm-Olam International offers all of that and more! We are a company that strives to deliver cost-effective, quick-to-market clinical services in today’s emerging marketplace. Pharm-Olam International has one of the largest global footprints … MORE INFO

Contracts Analyst - Clinical Research

Monster.com

NC-Durham, If you’re interested in working for a leading, mid-size Contract Research Organization (CRO) that has a massive global reach, then look no further, because Pharm-Olam International offers all of this and more. We are a company that strives to deliver cost-effective, quick-to-market clinical services in today’s emerging marketplace. Pharm-Olam has one of the largest global footprints of any CRO tod … MORE INFO

Medical Writer

Monster.com

NC-Morrisville, Worldwide Clinical Trials (WCT) is a leading therapeutically focused Contract Research Organization (CRO) that applies deep therapeutic expertise to help customers achieve their drug development goals. WCT’s global footprint, full complement of development service offerings, and innovative use of proprietary and cutting edge technology, bring about an environment which allows us to focus on identi … MORE INFO

Auditor Principal Specialist GCP

Monster.com

NJ-Bridgewater, Auditor Principal Specialist GCP Requirements: - Bachelor degree preferably in a life / medical / natural sciences or scientific discipline - 10 to 14 years of pharmaceutical (or related) experience with BA or 8 to 12 years with advanced degree, e. g. MBA, MS, PharmD, PhD. This includes a minimum of 6 years of Clinical Quality Assurance related experience and/or experience in Clinical Trials such a … MORE INFO

Regulatory Submissions Specialist

Monster.com

NY-Tarrytown, Requirements: -Bachelor's Degree (preferred) -Must have exp w/Modules 1-5 -3-5 Years of experience -Requires knowledge of applicable Regulatory Agency regulations, guidelines, and/or specifications (eg, FDA, EMA, ICH, etc). -Requires eCTD knowledge. -Strong knowledge of Microsoft Office suite, Adobe Acrobat, ISIToolbox and/or A-Pulse, electronic document management systems (SharePoint preferred), … MORE INFO

Regulatory Document Specialist

Monster.com

NJ-Basking Ridge, Responsible for independently formatting and publishing electronic documents for regulatory submissions. Integrates and applies strong knowledge of US electronic regulatory submission requirements in support of ongoing drug development programs. Independently formats and publishes electronic regulatory submission documents and ensures quality, accuracy, and submission readiness per regulatory agen … MORE INFO

Associate/Assistant Director, Economic Modeling and Outcomes Research (Remote Position)

Monster.com

PA-philadelphia, About Xcenda Xcenda, a business unit of AmerisourceBergen Corporation, is an integrated, world-class health care consulting organization focused on value, reimbursement and patient access. For more than 2 decades, Xcenda has helped global biopharmaceutical companies as well as emerging early-phase firms successfully commercialize innovative medical treatments and technologies in complex and cost-c … MORE INFO

Clinical Pharmacologist/Toxicologist

Monster.com

NJ-Princeton Township, Clinical Pharmacologist/Toxicologist Beta Pharma, Inc is seeking a driven Clinical Pharmacologist/Toxicologistto manage all nonclinical and preclinical affairs, including clinical pharmacology and toxicology development strategy, design and management of nonclinical and preclinical studies. The successful candidate will additionally manage CRO selection and oversee timelines and budgets. Beta Phar … MORE INFO

Research Assistant

Monster.com

NY-New York City, Premier Retina practice seeks a Research Assistant for its Manhattan location. The Research Assistant will work with the Research Coordinator in research related tasks to ensure all clinical trials and investigators ar conducted in an accurate and timely fashion, and in accordance with federal (Food and Drug Administration) regulations, Good Clinical Practice guidelines and Vitreous Retina Macula' … MORE INFO

Pharmaceutical Sales Rep - NYC Territory

Monster.com

NY-New York City, Rapidly expanding Pharmaceutical firm has an immediate need for a Sales Specialist who will be responsible for effectively applying promotional and selling strategies while growing theirproduct base for the firm in the New York City territory (specifically Manhattan). It will be this individual’s responsibility to provide medical and highly technical expertise to ensure awareness and appropriate u … MORE INFO

Regulatory Affairs Specialist

Monster.com

CA-Dublin, Our Client is looking for a Regulatory Affairs Specialist to join their team here in the SF Bay Area! Regulatory Affairs Specialist Duties: - Review study site start-up documentation, safety management plans and updates for global Phase 1-3 development programs. - Follow investigational medicinal product label translation process and archival - Collect Regulatory information to support QP product … MORE INFO

Research Assistant

Monster.com

CA-Fullerton, Position Summary: Proove Biosciences, Inc. is seeking team players for Research Assistantsto join a fast growing team supporting physician clinics across the nation. Proove Biosciences is the Personalized Pain Medicine Company. Our mission is to Change the Future of Medicine. With offices in Irvine, California and Annapolis-Junction, Maryland, Proove provides physicians with information to improve … MORE INFO

Research Assistant

Monster.com

CA-Irvine, Position Summary: Proove Biosciences, Inc. is seeking team players for Research Assistantsto join a fast growing team supporting physician clinics across the nation. Proove Biosciences is the Personalized Pain Medicine Company. Our mission is to Change the Future of Medicine. With offices in Irvine, California and Annapolis-Junction, Maryland, Proove provides physicians with information to improve … MORE INFO

Regulatory Documentation Specialist

Monster.com

NJ-Woodcliff Lake, Regulatory Documentation Coordinator You're precision-oriented and a stickler for doing it right. You have deep expertise in pharmaceutical compliance and quality control. Your critical thinking prowess makes you a problem solver extraordinaire. You generate powerful ideas and know how to get them implemented. If this describes you, this opportunity from Experis is just right for you.
· This is a o … MORE INFO

Clinical Data Management Manager

Monster.com

CA-Los Angeles, Our client, a global medical device company, is seeking a full time Clinical Data Management Manager in their Los Angeles area office. We are seeking an experienced, high caliber Clinical Data Management Manager (CDM). Working without appreciable supervision, the CDM has primary management responsibility directly or through subordinates for data related to clinical studies conducted by company. Ac … MORE INFO

Clinical Records Coordinator I

Monster.com

NC-Research Triangle Park, United Therapeutics Corporation is a biotechnology company focused on the development and commercialization of unique products to address the unmet medical needs of patients with chronic and life-threatening conditions. We have four approved products on the market today and we are not stopping there! From the United States to Europe to the Asia Pacific, we are proud of our multicultural business e … MORE INFO

Lc/ms/ms Scientist

Monster.com

NJ-Princeton, Research Scientist (LC/MS/MS) Sciex API 3000/4000 Also seek Bionalytical Project Manager / Principal Investigator Employee performs laboratory functions required for extraction and/or analysis of drugs from biological samples in support of pharmaceutical discovery, validation and sample analysis studies. Work is performed using bioanalytical division and GLP guidelines and applicable SOPs for anal … MORE INFO

Shown below: Corona clinical research area jobs provided by Indeed job search

Project Coordinator, Clinical Development - Device

Allergan, Inc. – Irvine, CA – Indeed.com

Research & Development. Project Coordinator, Clinical Development - Device. The Clinical Development team is an integral part of R&D leading and supporting the. . . … MORE INFO

Coordinator-Regulatory Affairs

Loma Linda University – Loma Linda, CA – Indeed.com

High-level professional research association training/education from Society of Clinical Research Associates (SOCRA) or Association of Clinical Research. . . … MORE INFO

Project Manager - R&D

Allergan, Inc. – Irvine, CA – Indeed.com

Research & Development. Systems & Data Support Responsibilities/Accountabilities. To this end, we employ more than 50 percent of our work force in either. . . … MORE INFO

Assistant Clinical Supervisor

People's Care, Inc. – Riverside, CA – Indeed.com

Assistant Clinical Supervisor. Assist Clinical Supervisor, Program Manager and Director with clinical and administrative tasks. . . . … MORE INFO

Clinical Research Associate I

Covidien – Irvine, CA – Indeed.com

Clinical Research Associate. Clinical research that leads to saving lives. Working knowledge of Good Clinical Practice (GCP) guidelines. . . . … MORE INFO

Principlal Regulatory Affairs Specialist

Covidien – Irvine, CA – Indeed.com

Work with cross-functional personnel in Research and Development, Clinical Affairs, Marketing, Quality, Operations, and Supply Chain. . . . … MORE INFO

Clinical Research Coordinator

University of California - Irvine – Irvine, CA – Indeed.com

Clinical Research Coordinator. Under the direction of the Principle Investigator, the Clinical Research Coordinator position coordinates the research efforts of. . . … MORE INFO

Preclinical Research Manager

Sonendo, Inc. – Laguna Hills, CA – Indeed.com

Manage a research team Qualifications. This innovative and results oriented individual designs and manages non clinical studies and research program. . . . … MORE INFO

Clinical Research Nurse Manager - Hematology

Medical Group (Duarte, CA) – Duarte, CA – Indeed.com

Clinical Research Nurses, Clinical Trials Administrators. The Clinical Research Nurse Manager supports high quality research, customer service excellence and. . . … MORE INFO

Clinical Specialist CRHF Orange County

Medtronic – , CA – Indeed.com

Clinical Specialist level. Preferred for Clinical Specialist. Cardiac Rhythm Heart Failure (CRHF)seeks candidates who will meet our customer expectations by. . . … MORE INFO

Clinical Research Associate

DOCS – Irvine, CA – Indeed.com

€ Knowledge of clinical and outcomes research study design. € 3-5 years experience directly supporting clinical research or similar experience in a medical. . . … MORE INFO

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Employment information for Corona, CA

5 year unemployment rate for
Riverside, CA (includes Riverside, San Bernardino, and Ontario metro areas) - continue for more info

14.3%
Year
13.6%
Year
12.0%
Year
10.2%
Year
9.0%
Year

Updated to reflect Jul 2014 unemployment rates

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