25 Clinical Research job listings in the Corona, California area

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Job listings, help wanted ads and employment postings (last updated on Tuesday, October 13)

Global Clinical Trial Manager


PA-Horsham, Job Title: Global Clinical Trial Manager Position Description Accountable for the successful execution of clinical activities assigned by the Functional Manager, Clinical Program Leader or Clinical Operations Head, within agreed timelines and budget, in alignment with all the applicable SOPs and regulatory requirements. Leads the Study Management Team (SMT) and interfaces with the correspondent Cl … MORE INFO

Medical Technologist


GA-Atlanta, Growing clinical laboratory in the metro Atlanta area seeking to hire Technologists for their Quality Control, Production/Manufacturing departments this fall. Positions are Permanent with excellent benefits. Role Highlights in Quality Control include:
· 1st shift hours available, No weekends.
· Performing laboratory testing and chemical evaluations of products according to SOP’s within defined tim … MORE INFO

CRO Lab Director and Principal Investigator jobs


NJ-New Brunswick, CRO Lab Director Manages ELISA method development and validation in New Jersey Project Manager / Principal Investigator with ELISA also needed in NJ, MD and Utah Lab Director Job Description: Responsible for overall laboratory operations and technical conduct of biotechnology method development, method validation and sample analysis projects, including the interpretation, analyses, documentation, … MORE INFO

Principal Investigator / Project Manager over Large Molecule


MD-Gaithersburg, Biotechnology Principal Investigator / Project manager Responsibilities:
· Responsible for client interaction and the conduct of studies.
· Responsible for data interpretation, analysis, and reporting of results for method development and validation of biopharmaceutical products.
· Responsible for the data interpretation of biologics, vaccines, and analysis of preclinical and clinical samples.

Principal Investigator / Project Manager with ELISA


NJ-Princeton, PRINCIPAL INVESTIGATOR — IMMUNOCHEMISTRY (also seeking CRO Lab Director and PMs in MD, UT, IN) Job Description:
· Overall responsibility for client interaction and the technical conduct of a study, as well as, for the interpretation, analysis, documentation, and reporting of results on Immunochemistry projects.
· Represent the single of point of control for research projects.
· Manage client relat … MORE INFO

Statistician / R / SAS


NJ-Raritan, Job Description: Reporting into the Statistical Leader, provide statistical review, input, and interpretation statistical analysis plans, topline reports, clinical study reports, and publications Author statistical analysis plans, top line reports, collaborate on clinical study reports, and provide guidance into the creation of the appendices thereof. Independently develop and apply appropriate st … MORE INFO

Senior Associate, Regulatory Affairs


NJ-Princeton, At Dr. Reddy’s, a global pharmaceutical company, you will contribute to making the breakthroughs of tomorrow a reality today! From making medicines more affordable to discovering innovative treatment options to satisfy unmet medical needs, we are dedicated to helping people lead longer and healthier lives. We are seeking dynamic and energetic individuals ready to inspire, ready to make a differenc … MORE INFO



CA-san diego, Regulus Therapeutics Inc. (NASDAQ: RGLS) is a biopharmaceutical company leading the discovery and development of innovative medicines targeting microRNAs. Regulus has leveraged its oligonucleotide drug discovery and development expertise to develop a well-balanced microRNA therapeutics pipeline complemented by a maturing microMarkersSM biomarkers platform and a rich intellectual property estate to … MORE INFO

Clinical Quality Control Reviewer


PA-Collegeville, Position details Job Title: Clinical Quality Control Reviewer Duration: 12+ months contract Client Location: Pennsylvania 19426-United States Description Responsibilities Data Quality Review / Quality Control (DQR/QC) Independently performs DQR/QC on clinical components of assigned documents (eg, clinical study reports, investigator brochures, manuscripts, summary documents, regulatory responses, … MORE INFO

Assistant Research Scientist


NY-New York City, Assistant Research Scientist Immunology & Autoimmunity An assistant research scientist position is available for an ambitious and productive applicant within the NYULMC Lupus laboratory. The successful candidate is expected to have basic laboratory experience in immunology. The main disease under study is anti-Ro associated congenital heart block but other aspects of human lupus, including vascula … MORE INFO

Senior Project Manager, R&D Project Management


NJ-Jersey City, Senior Project Manager, R&D Project Management Requirements: -A Bachelor’s Degree in Life Sciences or Engineering discipline; Advanced degree preferred -Must have experience within a Formal Project Management department, not just being a project manager in another department -7 years’ experience in pharmaceutical R&D environment or equivalent is required, combined with either/or experience above a … MORE INFO

Regulatory Compliance Officer


MA-waltham, Regulatory Compliance Officer Requirements: - Bachelor’s +5 years (Pharm D. , Health/Lifesciences) with at least two years’ experience in Pharmacovigilance / Pharmaceutical environment & safety in an international environment. - Advanced degree preferred -In depth understanding of international pharmacovigilance requirements/updates in particular EU/FDA requirements/international guidelines, e. g. I … MORE INFO

Health Sciences Research Contract Officer


CA-Los Angeles, UCLA Health offers health professionals the widest range of opportunities to practice the kind of care that every patient deserves. For more than half a century, we have provided the best in health and the latest in medical technology to the people of Los Angeles and throughout the world. If youre interested in being a part of one of the most comprehensive and advanced health systems on the planet … MORE INFO

Compliance Administrator


CA-Sunnyvale, We are seeking a Compliance Consultant for a 6 initially a 6 month contract in Sunnyvale, CA. Interested candidates should forward word doc resume with best contact information/time to speak. Thanks in advance. Consulting Compliance Contractor Primary Job Function
· The Consulting Compliance Contractor position will act as the primary liaison supporting Business Units for all Annual Planning, Need … MORE INFO

Associate Director, Project Management


MultiLocation, Role: Provides leadership, mentoring, and support to the project management team to help meet overall business goals and objectives, while maintaining management responsibility for all personnel, revenue, profit, and contracts. Job Functions/Responsibilities: Manages a team of Senior Project Manager(s), Project Manager(s) and may be assigned additional supportive staff within the project managemen … MORE INFO

Clinical Trials Assistant


TX-Fort Worth, Seeking a Clinical Trials Assistant for a consulting position at a pharmaceutical client in Fort Worth, TX 76134. Job Purpose: Assist Clinical Trial Management to ensure accurate, timely, and coordinated availability of clinical trial materials and documents. Mentor and assist with training of incoming CTAs. Assist with process improvement efforts. Major Accountabilities: 1. Enter and maintain cur … MORE INFO

Customer Service Associate


TX-Spring, Customer Care Associate — Full Time ID Number: 15-027/ 15-049/ 15-050 Location: The Woodlands, TX Department: Customer Care Reports to: Customer Care Manager Location: The Woodlands, TX Job Summary: Responsible for ensuring the satisfaction of customers by meeting and exceeding service expectations. Routinely interacting within the Customer Care department and interdepartmentally to relay customer co … MORE INFO

Clinical Research Coordinator


OK-Oklahoma City, WHAT YOU'LL BE DOING Serve as a research professional resource regarding the oncology clinical trials, protocol procedure and protocol compliance for physician, nurse, radiation therapist and other health care professional at the assigned center. Prepare protocol submission with the applicable IRB. Assist PI in writing protocol when delegated. Assist in obtaining and maintaining membership with co … MORE INFO

Senior Clinical Research Associate


MO-Kansas City, The Senior Clinical Research Associate will be responsible for consistently completing on site monitoring in accordance with project specific timelines. The Senior Clinical Research Associate will also be responsible for completing site monitoring reports, monitoring EDC data entry, and providing content for team meetings. The Senior Clinical Research Associate will have the following responsibili … MORE INFO

Clinical Research Protocol Analyst


PA-Horsham, Role: The primary role of the Clinical Research Protocol Analyst will be to review RFP material (protocol and related documents), appraise new and current business opportunities to include proposal planning, recruitment strategy development and operational implementation. Individuals must demonstrate a comprehensive understanding of clinical research patient recruitment across multiple therapeutic … MORE INFO

Medical Writer


MA-Raynham, We have an immediate position for a “Medical Writer” with our direct client (Top Pharmaceutical Company), if you are interested please send your updated resume to resume@collabinfo. com or please call 732-788-3483. Title: Medical Writer Duration : 7+ Months Location : Raynham, MA / West Chester, PA The Medical Writer Specialist is responsible for preparation of documents that support the presentati … MORE INFO

Clinical Data Coordinator


NJ-Princeton Township, We have an immediate position for a “Clinical Data Coordinator” with our direct client (Top Pharmaceutical Services Company), if you are interested please send your updated resume to chris@collabinfo. com or please call 732-788-3483. Title: Clinical Data Coordinator Duration : 6+ Months Location : Princeton, NJ or Conshohocken, PA Job responsibilities may include: Serve as a member of the project t … MORE INFO

Drug Safety Coordinator


NJ-Greystone Park, We have an immediate position for a “ Drug Safety Coordinator ” with our direct client (Top Pharmaceutical Company), if you are interested please send your updated resume to resume@collabinfo. com or please call 732-788-3483. Title: Drug Safety Coordinator Duration : 6+ Months Location : Morris Plains, NJ Responsible for the receipt and data entry of adverse event reports following Company Standard … MORE INFO

Site Activation Lead


PA-North Wales, Do you have experience in Global/Regional Study Start Up initiatives and are now looking to further develop, implement and execute a Study Start Up Strategy from site identification to site initiation visits as a site activation lead? As a site activation you, you would advance clinical trial start-up activities by understanding the client objectives and assist in the development of the plan for c … MORE INFO

Senior Health Economics Outcomes Researcher


MD-Bowie, Company Overview: Inovalon is a leading technology company that combines advanced cloud-based data analytics and data-driven intervention platforms to achieve meaningful insight and impact in clinical and quality outcomes, utilization, and financial performance across the healthcare landscape. Inovalon's unique achievement of value is delivered through the effective progression of Turning Data int … MORE INFO

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