25 Clinical Research job ads & opportunities in the Corona, California area

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

In House CRA


NJ-Morristown, In House CRA Requirements: -BA/BS -Minimum 1 year experience working on a clinical trial in a CTA, CRA, Project Associate type role -Phase 1 experience -They will take a monitor that wants to come in house -CNS experience preferred but not required -Junior level candidate -Study start up and close out experience -CNS Therapeutic area -Proofreading, filing experience, this is a support role -Projec … MORE INFO



MI-Livonia, LAB TECHNICIAN CHEMIST - LAB TECHNICIAN CHEMIST Set up, calibrate and operate laboratory instrumentation such as analytical balances, titrators, FTNIR o Operate computer controlled instrumentation and be able to store and extract data. o Prepare solutions, standards and buffers according to standard formulas used in analytical analysis. o Prepare quality control production samples o Prepare final … MORE INFO

CLINICAL TRIAL DIRECTOR, SPH Center for Global Health & Development (7698/D2115)


MA-BOSTON, The Clinical Trial Director will oversee all managerial aspects of the clinical trial, the efficacy and safety of Levofloxacin for the treatment of Multi-Drug Resistant Tuberculosis (Opti-Q), under the direction of the Principal Investigator. The selected candidate will be responsible for coordinating all aspects of the study, including monitoring progress at sites in Peru and South Africa, coordi … MORE INFO

Clinical Research Coordinator


GA-Atlanta, Description: Job Purpose: Supports clinical trials by planning, collecting, screening, and summarizing information gathered. MUST BE DETAIL ORIENTED, TEAM PLAYER WITH STRONG WORK ETHIC. COMPUTER SKILLS, PHLEBOTOMY AND EXPERIENCE WITH DIRECT PATIENT CONTACT ARE ABSOLUTE REQUIREMENTS. We will train the right candidate. Experience is a plus but not an absolute requirement. This is a job with unlimite … MORE INFO

Project Data Lead


PA-Warrington, If you have a background in clinical data management combined with the experience of creating edit checks, developing data delivery specifications, data management plans, and reports, learn more about how you can be a part of growing Clinical Research Organization that offers continued growth in the field of Data Management. About the Project Data Lead role within ICON: The Project Data Lead will … MORE INFO

Associate Scientist


NY-East Syracuse, Position Details: Position: Associate Scientist Location: East Syracuse, New York Duration: 06+ Months Contract Job Description : The role of the Research Scientist is to conduct experiments for the purposes of commercial support for downstream biopharmaceutical manufacturing. The candidate will support ultrafiltration/diafiltration, filtration, bulk fill, freezing, storage and cold chain shipping … MORE INFO

Clinical Monitor


PA-North Wales, Must have: - Medical degree (MD or equivalent), or other relevant doctoral degree (e. g. , PhD, PharmD) - Minimum 1-3 years in drug development and in the development and monitoring of clinical studies. - Familiarity with Good Clinical Practice (GCP) in clinical trials is mandatory Responsibilities: Under the general direction of TA head or designee, the Clinical Monitor has the primary responsibili … MORE INFO

Senior Clinical Research Associate


MN-Chaska, Senior clinical research associate to design and execute internal and external clinical studies for new & improved in-vitro diagnostic products. Must have experience in organizing and monitoring clinical trials, including site selection, identifying potential investigators, ensuring adequacy of clinical research staff/facilities. Responsibilities: Trains and monitors clinical trial sites to ensure … MORE INFO



MN-Chaska, Responsibilities include: Preparing and testing production and pilot reagents according to written procedures and protocols Performing simple calculations according to procedures, and maintaining accurate records of work performed according to GLP, GMP, and QSR s Explaining work processes to peers and may assist in training new employees Participating on a CPI Team, and contributing to team effort … MORE INFO

Data Collector


NE-Omaha, Do you have a passion for providing accurate information? Are you interested in data collection? Do you love to work flexible hours? If so, then you might be a great fit for a new part-time Data Collector position with Headway Workforce Solutions and RetailData! Since 1988, RetailData has defined and refined the data collection process. They specialize in the collection of competitive pricing and … MORE INFO

Clinical Research Associate - Remote


Telecommute/home-based, We have an immediate position for a ”Clinical Research Associate” with our direct client (Top Pharmaceutical services company), if you are interested please email your updated resume to nancy@collabinfo. com or call at 732-788-3483 Job Description : Clinical Research Associate FT Permanent Remote based Our Client is hiring experienced CRAs / Clinical Research Associates in our Early Clinical Develo … MORE INFO

Clinical Project Manager


NJ-Raritan, We have an immediate position for a “ Clinical Project Manager “ with our direct client (Top Pharmaceutical Company), if you are interested please send your updated resume to nancy atcollabinfo. com or nancy@collabinfo. com or please call 732-788-3483. Title: Clinical Project Manager Location: Raritan, NJ Duration: 2 Years Preclinical Project Manager The Project Management Office (PMO) is part of th … MORE INFO

Manager - Statistical Programmer


NJ-Princeton Township, We have an immediate position for a “Manager, Statistical Programming” with our direct client (Top Pharmaceutical services company), if you are interested please email your updated resume to nancy@collabinfo. com or call at 732-788-3483 Job Description : Statistical Programmer - Manager ( FT Permanent ) Location : Princeton, NJ Job Responsibilities: • Supervision of less-experienced statistical prog … MORE INFO

Validation Analyst


IL-Park City, Job Title: Validation Analyst Position Responsibilities Lead/support validation efforts and deliverables for systems used for Clinical, Pre-clinical, Global Medical Affairs and Finance / Operations with minimal oversight. Develop the validation testing strategy for large and medium sized projects and develop the overall Validation plans and timetables. Create and execute validation test scripts an … MORE INFO

Clinical Coordinator


CA-Downey, Coordinator Role: A study coordinator (SC) is a specialized research professional that works with and under the direction of a Principal Investigator (PI). Although the PI is predominantly responsible for the overall design and conduct of the clinical trial, the SC plays an integral role in supporting and facilitating the daily activities of the clinical trial. The SC works with the PI, the study … MORE INFO

Research Scientist II


MD-Edgewood, Ke`aki Technologies, LLC, is a Native Hawaiian Organization (NHO) owned business. A premier government services company, Ke`aki Technologies 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, when they need it … MORE INFO

Medical Publications Project Manager


IL-Bannockburn, Job Title: Medical Publications Project Manager Position Description Manage processes and publication related systems to ensure timely and transparent development of high quality scientific publications in support of neurology product portfolio. Responsible for providing project management oversight for the integration of publication management technology, reviewing publication drafts for scientif … MORE INFO

Senior Clinical Research Associate


IL-North Chicago, Job Title: Senior Clinical Research Associate Position Description Member of the clinical team will be responsible for late stage drug development according to Federal Regulations and ICH guidelines. This would include writing study protocols, planning study conduct, interacting with study team members, training of study investigators, planning and running study meetings and providing clinical fee … MORE INFO

In-House Clinical Research Associate


MA-Lexington, Job Title: In-House Clinical Research Associate Position Responsibilities This In-House CRA will be supporting the Clinical Operations study team members with various clinical trial activities including but not limited to: Review of regulatory documents Filing of study documentation in Company Trial Master File (TMF) Quality Review of CRO maintained TMF: Ensures proper and timely filing of all rel … MORE INFO

Biostatistician - Nationwide home or office based - PK/PD, PQT


KS-Overland Park, PURPOSE Prepare analysis plans and write detailed specifications for analysis files, tables, listings and figures. Interpret analyses and write statistical sections of study reports. Provide training, guidance and mentorship to lower level and new staff. RESPONSIBILITIES
· Develop analysis plans, table shells, programming and table specifications; produce tables, listings and figures; perform data … MORE INFO

Statistician/SAS/SDTM(Remote),Medidata,Supply Chain,Bioinformatic/Postdoctor,PK/PD/Pop


PA-Malvern, TechData is looking for multiple positions for Biostatistician and SAS programmer (Some positions can be remote), SDTM/Clinical Database Programmer, Metadata Repository (MDR) Global Librarian, Supply Chain Data Analyst, Sr. Research Investigator (Bioinformatics Analyst or Postdoctor in Genome), Pharmacometrician (Sr. Pharmacometrician, PK/PD analyst/Population PK)for our pharmaceutical clients in … MORE INFO

Director of Clinical Research - Clinical Research & Development


NJ-Parsippany, CyberCoders Matching Great People with Great Companies Learn more about CyberCoders Apply Director of Clinical Research Parsippany, NJ Unspecified Apply Apply Director of Clinical Research Parsippany, NJ Unspecified Apply Job Details Seeking a Director Clinical Research to execute clinical development plans, for defining the clinical trial strategy and management of all Phase 1-3 clinical studies … MORE INFO

Clinical Research Quality Assurance Associate


FL-Orlando, We are recruiting for a Quality Assurance Associate for Pharmaceutical Clinical Trial company located in Orlando Florida.
· Must have experience Auditing Clinical Trials
· Qualified candidates would need to have a Bachelor's degree in life sciences, nursing or any other relevant discipline. Candidates will also need to have a minimum of 4 years of QA experience in the pharmaceutical research indust … MORE INFO

Sr Scientific Medical Writer


TX-Fort Worth, The Scientific Medical Writer will oversee and supervise all writing (in-house and outsourced), with the exception of manuscripts prepared for external publication, for Global Medical Clinical Affairs, Americas, AWM, S&N, and for all other writing requests from within R&D. This role will be responsible, together with the Director, for writing assignments and delegation of projects, both in-house a … MORE INFO

Process Validation Coordinator


MA-Andover, Description: The primary focus of this position is to provide sample management and associated logistical support during a drug substance process validation campaign. Key responsibilities: Create and maintain master sample plan by assembling sampling requirements from all applicable activities, laboratories, and stakeholders associated with the process validation campaign Maintain and enforce samp … MORE INFO

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