29 Clinical Research job openings in the Corona, California area

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Job listings, help wanted ads and employment postings (last updated on Thursday, October 30)

Clinical Project Manager

Monster.com

PA-Philadelphia, Responsibilities Responsible for development, implementation, management and completion of oncology clinical research studies as well as related projects. Tasks include but are not limited to: developing and delivering project bid proposals, national and international project leadership, developing project teams over multiple clinical trial responsibility areas, SOP and project plan development an … MORE INFO

Clinical Education Manager

Monster.com

NY-New York City, Responsibilities Work closely with the Territory Managers to build brand awareness, educate physicians, implement and close evaluations and generate a strong sales pipeline to ensure sales targets are met or exceeded. Train providers and staff on the product in a way that inspires them to come to depend on the tools and mapping feature of the company colposcope. Continually provide customer feedba … MORE INFO

Sr Director, Development - Oncology

Monster.com

CA-San Diego, Job Number: 424269 Sr Director, Development - Oncology OVERVIEW This position directs the activities of the Oncology Product Development group. Provides the vision and leadership to develop end-to-end (sample-to-report) solutions for the oncology market. Focus areas are applications in screening for cancer, theranostics and monitoring drug response. Tasks and Responsibilities: Conducts and collabo … MORE INFO

Business Analyst 2

Monster.com

NC-Durham, Quintiles pioneered the idea of helping pharma companies conduct objective clinical trials to establish not only whether a drug is effective, but who can take it safely. Our customers have relied on us to design and conduct rigorous clinical research for decades, from small studies to multinational mega-trials. However, we continue to develop new ways of interpreting and evaluating data that allow … MORE INFO

Associate Director of Toxicology

Monster.com

NJ-Princeton Township, Associate Director of Toxicology Beta Pharma, Inc is seeking a competentAssociate Director of Toxicologyfor all aspects of Preclinical Development including the design, development and direction of toxicology, immunological, pharmacology and pharmacokinetics studies. Beta Pharma, Inc is an emerging specialty pharmaceutical company dedicated to the discovery, development and commercialization of in … MORE INFO

Chemist

Monster.com

PA-Lancaster, Consider joining Eurofins Lancaster Laboratories where people are the most important element in our chemistry. Celebrating 50 years of service, Eurofins Lancaster Laboratories is a leading contract lab providing testing and research services in the environmental, pharmaceutical, and biopharmaceutical sciences to clients worldwide. Eurofins Lancaster Laboratories, a nationally recognized laboratory … MORE INFO

Aseptic Fill Program Manager

Monster.com

NC-Durham, Under the supervision of the Industrial Process director, the candidate is responsible for activities involved with the drug product (vaccine) filling operations. This candidate will oversee all operations performed by CMOs dealing with filling product, placebo and adjuvant. In addition the candidate will be responsible for assuring operations conform to quality agreements, writing and / or review … MORE INFO

Statistician/SAS Programmer(Remote),Manager of CDISC Programming,Mongo DBA,Medical Information Assoc

Monster.com

MA-Cambridge, TechData is hiring SAS Programmer (some positions can be telecommute) and Biostatistician (Some positions can be telecommuting), Manager of clinical data/CDISC programming, Statistical Programmer for observational study/outcome research, Database Administrator III: Database Administrator III/MongoDB DBA, Medical Information Associate for our pharmaceutical clients in Cambridge MA, Cambridge, Boston … MORE INFO

Clinical Research Associates (CRAs) $5K Sign On Bonus http://jobsearch.covance.com/49221-jobs.aspx

Monster.com

WA-Seattle, Experienced CRAs needed for Early Clinical Development (Phase I & IIa). MUST have Phase I and/or Oncology Experience!
· $5,000 Sign On Bonus
· COVANCE is focusing on balance and quality by only working on 1 to 2 studies! The Clinical Research Associate conducts site monitoring responsibilities for Clinical trials, according to Covance Standard Operating Procedures, ICH guidelines and GCP, including … MORE INFO

Data Analyst & Research Associate

Monster.com

NY-Irvington, This position reports to the Head of Clinical & Medical Affairs. Primary responsibility is to support clinical study and medical affairs activities including the following: - Data Analyst: Management of large study databases including, but not limited to, writing computer data checks utilizing formulas and data reporting. Perform basis statistical calculations on study data for clinical reporting. … MORE INFO

ProjectMgrManufacturing,AcctSupervisor

Monster.com

NJ-East Hanover, TechData Service is a top staffing company with openings for contract positions with many pharmaceutical companies in the NJ and PA areas. Currently we have the following openings with our top clients. We have openings for a Project Manager (Manufacturing experience), Accounting Supervisor, Outsourcing Manager, Sr. Account Trial Manager, Sr. Scientist, Safety Specialist, Statistical Programmer, an … MORE INFO

Sample Receiving Technician

Monster.com

GA-Atlanta, Sample Receiving Technician needed for full-time support in high volume research facility. Will organize and distribute samples to include: urine, whole blood, serum, etc. Will provide ongoing inventory maintenance of specimens. Must be a team player and have strong organizational skills and the ability to multi-task with large volumes of samples received on a daily basis. 1st Shift Hours — Monday … MORE INFO

Laboratory Technician 8

Monster.com

MD-Ft Detrick, Description: Ke’aki Technologies, LLC, is a Native Hawaiian Organization (NHO) owned business. A premier government services company, Ke’aki Technologies, LLC offers a full spectrum of solutions that improve the performance and operational effectiveness of our government and Department of Defense customers. Our mission synchronized solutions are designed to deliver exactly what our customers need, … MORE INFO

Regulatory CMC Manager

Monster.com

MA-Cambridge, Job Title: Regulatory CMC Manager Position Description This individual is expected to contribute to the development and implementation of CMC regulatory strategy for products in development with minimal supervision as well as coordinating all aspects of CMC regulatory submissions relevant to their assigned projects or programs. This person will serve as the regulatory CMC representative on relevan … MORE INFO

Senior Biostatistician

Monster.com

CA-Home Based, PAREXEL International Corporation is a leading global bio/pharmaceutical services organization, providing a broad range of knowledge-based contract research, consulting, and medical communications services to the worldwide pharmaceutical, biotechnology and medical device industries. Committed to providing solutions that expedite time-to-market and peak-market penetration, PAREXEL has developed sig … MORE INFO

Senior Clinical Data Analyst

Monster.com

NC-Home Based, PAREXEL International Corporation is a leading global bio/pharmaceutical services organization, providing a broad range of knowledge-based contract research, consulting, and medical communications services to the worldwide pharmaceutical, biotechnology and medical device industries. Committed to providing solutions that expedite time-to-market and peak-market penetration, PAREXEL has developed sig … MORE INFO

Clinical Project Manager

Monster.com

MN-Minneapolis, Our client — a global medical device company is looking for a contract Clinical Project Manager for their western Minneapolis suburb location. Position Summary: The Clinical Project Manager is responsible for managing and meeting the objectives of clinical projects regarding a new surgical technology assessment in Europe. Internally interfaces with data management, biostatistics, regulatory, clini … MORE INFO

GPT Project Manager - Influenza

Monster.com

MA-Cambridge, GPT Project Manager - Influenza Business Unit: Global Development Division: Vaccines & Diagnostics Company/Legal Entity: Novartis Job Reference Code: 151885BR Global Program Team for Influenza is seeking a GPT Project manager focusing on the Adjuvanted Programs. The GPT PM will be working closely with the Development Project Lead on an exciting line-up of projects, including the largest Phase III … MORE INFO

Research Scientist

Monster.com

CT-Bethany, Company Description Connecticut Analytical Corporation (CAC) was formed in 1989 as a medical instrument manufacturing firm. Since that time, activities have expanded to include instrument design, applied research, and medical diagnostic investigation. We proudly employ scientists and engineers with electrical, mechanical, chemical and biomedical backgrounds. CAC rapidly transforms theoretical rese … MORE INFO

1884 Senior Research Associate

Monster.com

AL-Dothan, Description: Laulima Government Solutions, LLC, is a Native Hawaiian Organization (NHO) owned business. A premier government services company, Laulima Government Solutions, LLC offers a full spectrum of solutions that improve the performance and operational effectiveness of our government and Department of Defense customers. Our mission synchronized solutions are designed to deliver exactly what o … MORE INFO

Regulatory Compliance Specialist

Monster.com

TX-San Antonio, Regulatory Compliance Specialist Clinical Trials of Texas, Inc. (CTT) is currently seeking a Regulatory Compliance Specialist for our regulatory department. The primary focus of this position is to ensure timely and accurate submission of regulatory and IRB documents for new and ongoing studies and to ensure that our research site is in compliance with CTT's SOPs, sponsor/CRO requirements, FDA reg … MORE INFO

QA/Statistician,SAS,Technical Writer,Drug Safety,Auditor,Recruiter,Software Develop,Data Entry

Monster.com

NJ-Bridgewater, TechData is hiring Quality Assurance Lead, Biostatistician, SAS Programmers(Some can be telecommuting), Technical Writer, Medical Writer, Auditor/Principal Specialist, Recruiter, Software Developer, Drug Safety Specialist, Trial Safety Manager, Clinical Data Manager, data entry coordinator in Central and Northern NJ. Please see below requirements and send your resume to: HR@techdataservice. com or … MORE INFO

Clinical Research Associate

Monster.com

MN-Minneapolis, 6 Month Contract Position - H1's/Subcontractors will NOT be considered:
· Assist in preparation of clinical protocols and FDA submissions.
· Perform site initiation and close-out visit, reviews and audit data collection forms, participate in Investigator Meetings, assist in physician training, train site research coordinators, develop study guides and SOPs, resolve queries, support animal lab work … MORE INFO

Foundation Program Manager

Monster.com

DE-Wilmington, Responsibilities: Excellent employment opportunity for a Foundation Program Manager in the Wilmington, DE area. Provide general support to the Foundation’s Executive Director to manage and administer the Foundation and its programs under the strategic direction of the Board of Trustees Manage and successfully deliver Foundation programs and special projects, including collaborating with key stakeh … MORE INFO

Research Assistant Job

Monster.com

CA-Palo Alto, Company: Yoh Research Assistant needed for a Contract opportunity with Yoh's client located in Palo Alto, CA. What You'll Be Doing: - Primary responsibilities will be to design and construct vectors, transformation of microbial strains, and evaluation of gene expression and protein production. - Candidate will also be expected to process data, in addition to recording and communicating results in … MORE INFO

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

Clinical Research Coordinator- Cardiac, SCRI Riverside, CA

Riverside Community Hospital – Riverside, CA – Indeed.com

Clinical research experience- 3 years. Knowledge of federal regulations, good clinical practices (GCP). Medical and research terminology. . . . … MORE INFO

Clinical Research Coordinator I

Advanced Clinical – Irvine, CA – Indeed.com

Qualified candidates must have experience working with clinical research studies. Responsible for the preparation of regulatory documents and functions as a. . . … MORE INFO

Clinical Research Coordinator

Association of Clinical Research Professionals – Chino, CA – Indeed.com

Catalina Research Institute, LLC is a fast growing, multi-specialty research site in Chino, California. We are looking for an experienced clinical research. . . … MORE INFO

Head, Clinical & Regulatory Operations

Axar Pharmaceuticals – Corona, CA – Indeed.com

GMP, GCP, GLP, DEA, OSHA guidelines, SOPs, etc;13. representing the Department in meetings with FDA as a Clinical/Regulatory head and in corporate project review. . . … 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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