Temporary Research Jobs in California
PRIDE Health
$1961 WEEK
Los Angeles, CA
PRIDE Health is the minority-owned healthcare recruitment division of Pride Global—an integrated human capital solutions and advisory firm. Pay package is based on 8 hour shifts and 40.0 hours per week (subject to confirmation) with tax-free stipend amount to be determined.
AMN Healthcare
$250000 - $360000 YEAR
San Francisco, CA
Participate in the I-SPY TRIALS, a groundbreaking national public-private collaboration among NCI, FDA, more than 20 cancer research centers, and major pharma and biotech companies, as well as the University of California-wide Athena Breast Health Network, a learning system designed to integrate clinical care and research as it follows 150,000 women from screening through treatment and outcomes. Join an internationally recognized breast cancer team in an NCI-designated Comprehensive Cancer Center, including breast surgeons, breast imagers, oncologists, radiologists, and pathologists, working collaboratively to revolutionize breast cancer screening and treatment throughout our nation.
University of California Agriculture and Natural Resources
$28.88 - $37.36 HOUR
Browns Valley, CA
Under the supervision of the Center Director, the incumbent will be responsible for collection, management, analysis of data and records related to all-natural resource and beef cattle research projects as well as Center maintained long term monitoring plots and databases. Incumbent will provide leadership and act as lead person to Agriculture/Animal Technicians, Farm Maintenance workers and Student Assistants on research projects these staff members assist with.
Abbott Laboratories
$86700 - $173300 undefined
Santa Clara, CA
Facilitates communication between Sales and Marketing, R&D, Clinical R&D, Regulatory Affairs, Library Services, Product Performance Group (PPG), Quality Engineering, Clinical Affairs or Clinical Science, Risk Management, Clinical Project Management, external CROs or Medical Writers, Training, Senior Management and investigational sites as directed by your manager. Our extensive portfolio includes drug-eluting stents, bare metal stents, guide wires, balloon dilatation catheters, imaging catheters and software, vessel closure devices and peripheral stents.
Abbott Laboratories
$86700 - $173300 undefined
Alameda, CA
Responsible for assisting senior staff in planning study conduct, designing case report forms (CRFs), conducting User Acceptance Testing (UAT), Contract Research Organization (CRO) selection and management, selection and training of investigator sites, planning and running study meetings, evaluation, selection and training of new study investigators and writing and assembling submissions. Solid understanding and demonstrated experience of the clinical trial process including study design and conduct; clinical data management systems; clinical trial management systems; data analysis; and data reporting and interpretation.
OSI Engineering
$40 - $50 HOUR
Mountain View, CA
Job Responsibilities:Develops product-critical physiological data-collection protocols and executes studies according to good laboratory practice, following applicable health and safety principles and practices. A global device company is looking for a motivated Clinical Research Associate III to support studies involving wearable sensor technology and human subject data collection.
Jobot
$25 - $26 YEAR
Santa Clarita, CA
A minimum of 1 year of experience in a chemistry laboratory, preferably within a healthcare or scientific industry. 6. Experience working with a Medical Group or similar healthcare teams - not required .
Jobot
$80 - $90 YEAR
Los Angeles, CA
Key Responsibilities: Under the direction of the Portfolio Manager the successful candidate will: Participate in both strategic planning and tactical execution of clinical research data projects in analysis and implementation; facilitate communications between project partners, clinical researchers and data scientists as they relate to supporting research data acquisition and utilization issues and provide oversight and direction to project team members. Qualified candidates preferred to have: PMP, extensive experience within University driven healthcare system or major EHR healthcare system, and oversee complex health data innovation and digital transformation initiatives, collaborating with clinicians, researchers, technical teams, and executive stakeholders to deliver impactful technology solutions that improve patient care and operational outcomes.
Jobot
$58 - $65 YEAR
Los Angeles, CA
Key Responsibilities: Under the direction of the Portfolio Manager the successful candidate will: Participate in both strategic planning and tactical execution of clinical research data projects in analysis and implementation; facilitate communications between project partners, clinical researchers and data scientists as they relate to supporting research data acquisition and utilization issues and provide oversight and direction to project team members. Maintain all status related communications with internal and external stakeholders (i.e., affected parties) Special Knowledge, Skills & Abilities: Experience leading a variety of multi-person projects simultaneously and comfortable switching gears depending on business requirements.
UC Berkeley School of Optometry
Berkeley, CA
The responsibilities of the health science clinical faculty members include teaching optometric student clinicians in the patient care environment, performing direct patient care when student clinicians are unavailable both on or off the UC Berkeley campus, and/or teaching optometric student clinicians the basics of eye examinations sequence in the pre-clinical environment. The Herbert Wertheim School of Optometry and Vision Science at the University of California, Berkeley invites applications for a pool of qualified health science clinical faculty members at the Clinical Instructor, Assistant, Associate, or Full Clinical Professor level to teach in the School of Optometry and Vision Science and/or Berkeley Optometry partner off-campus clinics, should an opening arise.
Bio-Rad Laboratories, Inc.
$40 - $50 HOUR
Pleasanton, CA
Embrace the importance of teamwork, share your knowledge, and actively engage with colleagues from diverse backgrounds, contributing to a collaborative and harmonious work environment that promotes innovative solutions and impactful research outcomes. Actual compensation will be provided in writing at the time of offer, if applicable, and is based on several factors we believe fairly and accurately impact compensation, including geographic location, experience, knowledge, skills, abilities, and other job permitted factors.
Jobot
$25 - $28 YEAR
Fresno, CA
The role involves providing comprehensive support to our senior executives, including administrative tasks, meeting coordination, travel arrangements, and other related duties. Manage executive email inboxes, prioritizing important communications, drafting responses, and flagging urgent messages.
Talent Software Services, Inc.
Los Angeles, CA
Establish and execute logistical aspects of clinical research projects to achieve objectives, including project planning, resource projection, and developing systems for protocol compliance and patient safety. Coordinate administrative functions of research studies, including scheduling patient research visits, procedures, and labs, and maintaining consent forms, case report forms, SAE's, and source documents.
Children's Hospital Los Angeles
Los Angeles, CA
The Clinical Research Assistant supports the Principal Investigator or other study team members with research studies which includes subject recruitment, data collection, scheduling of study-related activities and follow-up with enrolled subjects. As a premier Magnet teaching hospital, you’ll find an environment that’s alive with learning, rooted in care and compassion, and home to thought leadership and unwavering support.
Apidel Technologies
Pasadena, CA
The Lab Assistant may carry out various tasks in the office setting, including preparation of patient past sheets, verification of patient records/data entry, preparation of patient documents for billing purposes, dispersal of patient reports (fax, email, mail, etc.), among other administrative tasks. The Lab Assistant also carries out other general laboratory tasks, such as organizing, archiving, and pulling samples to and from freezers, taking temperatures of storage units, instrument maintenance tasks, routine inventory checks, among other laboratory duties.
Medpace, Inc.
$70000 - $160000 YEAR
San Francisco, CA
Responsibilities :Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward; Verification that the investigator is enrolling only eligible subjects; Regulatory document review; Medical device and/or investigational product/drug accountability and inventory; Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol; Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; and. Qualifications :Must have a minimum of a Bachelor’s degree in a health or science related field; Experience as a Clinical Research Coordinator (minimum 1 year); Ability to travel 60-70% to locations nationwide is required; some visits may be conducted remotely; Must maintain a valid driver’s license and the ability to drive to monitoring sites; Proficient knowledge of Microsoft® Office; Strong communication and presentation skills; and.
Medpace, Inc.
$70000 - $160000 YEAR
Los Angeles, undefined
Responsibilities :Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward; Verification that the investigator is enrolling only eligible subjects; Regulatory document review; Medical device and/or investigational product/drug accountability and inventory; Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol; Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; and. Ability to travel 60-70% to locations nationwide is required; some visits may be conducted remotely; Must maintain a valid driver’s license and the ability to drive to monitoring sites; Proficient knowledge of Microsoft® Office; Strong communication and presentation skills; and.
Bio-Rad Laboratories, Inc.
$33 - $39.95 HOUR
Hercules, CA
Actual compensation will be provided in writing at the time of offer, if applicable, and is based on several factors we believe fairly and accurately impact compensation, including geographic location, experience, knowledge, skills, abilities, and other job permitted factors. As one of the top five life science companies, we are a global leader in developing, manufacturing, and marketing a broad range of high-quality research and clinical diagnostic products.