26 Clinical Research job openings in the Fremont, California area

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

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

Clinical Trials Manager

Monster.com

CA-Pleasanton, BioPhase Solutions specializes in recruiting top talented professionals for California's Scientific community. We are recruiting for a Clinical Trial Manager, specializing in Cardiovascular Devices. This position is direct hire and located in the East Bay. Responsibilities: Manages Company-sponsored and clinical trials. Responsible for timelines and budgets for assigned trials. Enforce compliance … MORE INFO

Sr. Manager, Clinical & Applications Development

Monster.com

CA-Dublin, JOB SUMMARY: The Sr. Manager, Clinical & Applications Development, is responsible for the management of Company retina and glaucoma related regulated clinical studies in support of marketing applications in the United States and other countries as required. This role oversees the development of new ophthalmic diagnostic algorithms and applications, directing the software-focused advanced developme … 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

Sr. Clinical Research Associate

Monster.com

CA-Palo Alto, The Senior CRA will be responsible for monitoring “Device” studies. The candidate must have at least 5 -7 years of monitoring experience with 3 years being Medical Device. This is a full time contract position. Travel is 30%. Candidate must have at least a Bachelor's Degree. … 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

Laboratory Scientist (Bioinformatics)

Monster.com

CA-Redwood City, CyberCoders Matching Great People with Great Companies Learn more about CyberCoders Apply Laboratory Scientist (Bioinformatics) Redwood City, CA Contract Unspecified Apply Apply Laboratory Scientist (Bioinformatics) Redwood City, CA Contract Unspecified Apply Job Details Based in Foster City, CA we are a breakthrough diagnostic leader in technology working with high profile clients such as Mayo Cl … MORE INFO

Associate Research Scientist

Monster.com

CA-Redwood City, Position Details: Position: Associate Research Scientist Location: Redwood City, California, 94063 Duration: 6+ Months Contract (40 hrs/week) Description:
· At Client, we help develop some of the most exciting biologic therapeutics in the field of oncology, immuno-oncology etc. , through collaborative and integrated approaches.
· A temporary position, for 6 months, to work in the inter-disciplinary … MORE INFO

Verification Specialist

Monster.com

CA-San Jose, Position : System Verification Specialist Location : 2350 Qume Drive San Jose CA 95131 UNITED STATES Duration : 12 Months Contract Rate : $35. 00 /hr on W2 (All inclusive) Start Time : 8: 00 AM End Time : 5: 00 PM Total Hours/week : 40. 00 Client : Medical Devices/Biosciences EDUCATION AND EXPERIENCE :
· Typically requires a BS or MS degree in Immunology, Cell Biology, Biomedical Engineering or in a r … MORE INFO

Clinical Research Assistant

Monster.com

CA-Sunnyvale, Our client in the South Bay is looking for a Clinical Research Assistant to join their team! Job Duties
· Support Clinical Research team members
· Obtains, reviews, processes, and tracks study related documents such as CVs, FDA 1572s, lab certifications, IRB approvals, contracts, protocols, etc.
· Maintains and distributes basic study tracking information including: Visit Reports, Regulatory Docum … MORE INFO

Senior Site Manager / Site Manager

Monster.com

CA-South San Francisco, Our client in South SF is looking for a Senior Site Manager/Site Manager to join their team Responsibilities: - The Clinical Site Manager will assist in providing strategic and tactical planning, organization, directions and tracking to execute study - Assist the Project Manager in developing realistic trial plans including, site monitoring strategies, risk mitigation strategies, trial budgets, si … MORE INFO

Clinical Data Management Systems Project Manager

Monster.com

CA-South San Francisco, Our client in South San Francisco is looking for a Clinical Data Management Systems Project Manager to join their team! Duties - Manage the project lifecycle from initiation, planning, execution, control, and close out - Develop and implement project timelines including software validation and business process milestones - Regularly manage communications to business sponsors, project teams, and ma … MORE INFO

Staff Scientist

Monster.com

CA-South San Francisco, Our client in South San Francisco is looking for a Staff Scientist to join their team! JOB DUTIES: Lead development of applications and protocols for Single Cell Genomics. Define, develop, test and validate products for commercial release. Generate data to support marketing and sales. Work with bioinformatics team members to interpret data and develop methods for data analysis. Manage project sche … MORE INFO

Drug Safety Associate

Monster.com

CA-Brisbane, The Senior Drug Safety Associate (DSA) is responsible for: Establishing work priorities and direction independently with minimal input from Manager. Collecting, documenting, and processing adverse event (AE) reports from clinical trials and post-marketing sources in accordance with company Standard Operating Procedures (SOPs) and work practices to ensure and maintain regulatory compliance. This in … MORE INFO

Drug Safety Associate/Sr. Drug Safety Associate (DSA)

Monster.com

CA-Brisbane, Duties: The Senior Drug Safety Associate (DSA) is responsible for: Establishing work priorities and direction independently with minimal input from Manager. Collecting, documenting, and processing adverse event (AE) reports from clinical trials and post-marketing sources in accordance with company Standard Operating Procedures (SOPs) and work practices to ensure and maintain regulatory compliance. … MORE INFO

Clinical Data Quality Analyst

Monster.com

CA-South San Francisco, SF Bay Area BioPharma company is looking for a Clinical Data Quality Analyst that can step in and assist on a current project they have. If you have these skills, contact us ASAP! Duties:
· The department is seeking an experienced Clinical Data Quality Analyst who is motivated, data-driven and analytical to manage the Clinical data assets of the organization
· This individual will work in the Clin … MORE INFO

Clinical Research Manager (Remote Position)

Monster.com

CA-San Francisco, XCENDA SUMMARY: “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 … MORE INFO

Clinical Trial Associate Job

Monster.com

CA-San Francisco, Company: Yoh Clinical Trial Associate needed for a contract opportunity with Yoh's client located in South San Francisco, CA. What You'll Be Doing: - Complete task assigned by Local Study Team that will enable the team to meet project goals and deliverables for all phases of the clinical trial process - Tasks may include creating regulatory and general communication documents, coordinating interna … MORE INFO

Bioanalytical Project Manager / Principal Investigator

Monster.com

CA-san francisco, Project Manager / Principal Investigator Will you relocate? Seeking Project Manager with Lc/ms/ms in GLP labs in NJ, Utah and North Carolina Seeking Principal Investigator also with Large Molecule in Maryland Seeking Sr. Scientist with Lc/ms/ms method development in NJ and NC Position Purpose: To manage the daily activities of (pharmaceutical) studies. This position has overall responsibility for … MORE INFO

Regulatory Operations / Publisher

Monster.com

CA-Alameda, Our client in the San Francisco Bay Area is looking for a Regulatory Operations / Publisher to join their team. Regulatory Operations / Publisher Duties: - Perform submission build, compilation and publishing activities associated with generating hard copy and electronic submissions - Publish documents by creating bookmarks and hyperlinks in submission files according to ICH and FDA guidelines as … MORE INFO

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

Medical Science Liaison MS Northern California\Central Valley

Genzyme – San Francisco, CA – Indeed.com

The MSL will act as a conduit for providing accurate and updated clinical, scientific and medical information to MS Experts, health care professionals,. . . … MORE INFO

Senior Manager of Clinical Operations – Quality, Standards, and Processes

Onyx Pharmaceuticals – South San Francisco, CA – Indeed.com

Ensure compliance with Onyx SOPs and guidelines, FDA regulations, and current ICH GCP guidelines. Current knowledge of Code of Federal Regulations and ICH. . . … MORE INFO

Clinical Project Manager

Advanced Clinical – Santa Clara, CA – Indeed.com

Excellent knowledge of CFR, GCP, local regulations and internal procedures required for clinical trials; Proven record of compliance with, and enforcement of,. . . … MORE INFO

Clinical Research Coordinator

Stanford University – Stanford, CA – Indeed.com

1 year of experience working in clinical research or a combination of graduate level education and managing clinical research in a patient care setting. . . . … MORE INFO

Program Specialist (Regulatory Affairs and Clinical Compliance Auditor)

Department of Veterans Affairs – Mountain View, CA – Indeed.com

Ensures that the Center uses validated electronic systems and participates in that validation as appropriate, including assessing GCP impact of the systems. . . . … MORE INFO

Clinical Research Assistant

Align Technology – San Jose, CA – Indeed.com

Assist the Clinical Research team with monitoring and tracking patients in clinical activities. Has some knowledge of clinical research field. . . . … MORE INFO

Clinical Operations Associate

StemCells Inc. – Newark, CA – Indeed.com

Demonstrated knowledge of US clinical research regulatory requirements as described in ICH GCP Section 8, FDA 21 CFR and other applicable sources. . . . … MORE INFO

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Employment information for Fremont, CA

5 year unemployment rate for
San Francisco, CA (includes San Francisco, Oakland, and Fremont metro areas) - continue for more info

10.3%
Year
9.4%
Year
8.1%
Year
6.6%
Year
5.6%
Year

Updated to reflect Jul 2014 unemployment rates

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