Clinical Research Associate jobs in Escondido, CA

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CNS - Clinical Research Associate (CRA) - W2
  • C-Clinical
  • San Diego, CA FULL_TIME
  • C-Clinical

    Our clinical research firm is expanding and we have an opportunity for a Senior CRA with CNS, oncology, or metabolic experience for our pharmaceutical company client. The site monitoring is a hybrid model of risk-based remote and on-site monitoring. We are looking for CRAs with experience, who currently live in San Diego or Western US. This is for a W-2 contract. We have two openings at ~100%, and the same company is potentially looking for 1 FTE to hire internally.

    If you want to work for a great sponsor with career opportunities - look no further. Our group working with this client is rapidly growing, they enhance our clients' culture as well-established professionals - and we are all passionate about doing life-changing clinical research. We want to be in business with like-minded people. If you meet the qualifications and this sounds like you, apply today! Please fill out the intro application survey sent via email after you apply. Thank you!

    Responsibilities

    • Sr. CRA Western USA (On-site)
    • Interfaces with the study team to ensure timely initiation and completion of clinical trials
    • Responsible for the identification, evaluation, and qualification of investigators and sites
    • May prepare and submit essential document packages required for clinical site initiation
    • Performs on-site monitoring activities for clinical trials and escalates site issues to Clinical Trial Manager (CTM)/Project Manager (PM); documents activities in the monitoring reports and follow-up correspondence
    • Reviews and manages data on-site and remotely; resolves issues on a continuous basis to achieve timely database targets
    • May be responsible for all aspects of study site monitoring: pre-study visits, site initiation visits, routine monitoring visits, close-out visits of clinical sites, and maintenance of study files, with or without guidance
    • Ensure the protection of research subjects by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements
    • Identify, track, and follow up on all Adverse Events (AEs) and Serious Adverse Events (SAEs); ensure all applicable SAEs are reported to sponsor and regulatory authorities
    • Ensure the accuracy and integrity of the data submitted on electronic or paper case report forms (CRFs), or other data collection tools, by comprehensive source document review. Monitor the study database for missing or discrepant data compared to the source record at the clinical site
    • Ensure that all required monitoring tasks are conducted according to site SOPs, established guidelines, work instructions, and project plans (e.g., monitoring plan)
    • Maintain study blindly and act as a blinded study monitor. Conduct eCRF/CRF review, query generation, and resolution against established data review guidelines, with or without direct supervision
    • Attend investigators’ meetings, project team meetings, and teleconferences, as needed.
    • Understands and applies knowledge regarding local, state, country regulations (i.e., TGA, etc.) and ICH-GCP
    • Maintain training on ICH-GCP, study protocol, and client procedures
    • May track regulatory documents may track recruitment, may evaluate study site quality and integrity, and may motivate assigned sites to meet client deadlines
    • May be responsible for all aspects of study site monitoring: pre-study visits, site initiation visits, routine monitoring visits, close-out visits of clinical sites, and maintenance of study files, with or without guidance
    • Ensure the protection of research subjects by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements
    • Identify, track, and follow up on all Adverse Events (AEs) and Serious Adverse Events (SAEs); ensure all applicable SAEs are reported to sponsor and regulatory authorities
    • Ensure the accuracy and integrity of the data submitted on electronic or paper case report forms (CRFs), or other data collection tools, by comprehensive source document review. Monitor study database for missing or discrepant data compared to the source record at the clinical site
    • Ensure that all required monitoring tasks are conducted according to site SOPs, established guidelines, work instructions, and project plans (e.g., monitoring plan)
    • Maintain study blindly and act as a blinded study monitor. Conduct eCRF/CRF review, query generation, and resolution against established data review guidelines, with or without direct supervision
    • Understands and applies knowledge regarding local, state, country regulations (i.e., TGA, etc.) and ICH-GCP
    • Maintain training on ICH-GCP, study protocol, and client procedures
    Qualifications

    • 3 years or more as a CRA with site monitoring responsibility And 1 year or more CNS

    Or

    • 3 years or more as a CRA with site monitoring responsibility And 1 year or more in either: Phase 1, a complex indication with in-patient monitoring, Or metabolic studies

    Or

    • 3 years or more as a CRA with site monitoring responsibility And 1 year or more in Oncology Monitoring 

    And

    • The candidate possesses a 4-year university degree, ideally in a scientific field
    • In lieu of a 4-year university degree, a candidate with 7 or more years of relevant clinical research experience, nursing/possibly another medical certification, and 5 years of monitoring in a complex indication (in-patient, oncology, phase 1, etc.) may be considered
    • Must have working rights in the United States
    • Must be located within the West Coast within 1 hour of an airport
    • The candidate must have availability for this contract for at least 1 year
    • Must possess exemplary verbal skills in the English language with the ability to solve complex problems using medical terminology
    • Bi-lingual is a plus
    • Must be proficient at tactfully managing intra-team communication, as well as interpersonal communication
    • Note: the travel rate is 50% regular rate
    Compensation
    $65 - $89 hourly
    About C-Clinical

    C-Clinical is a clinical operations partner that provides highly specialized consulting services for the pharmaceutical, biotechnology, and device industries.


    Our chief concept is in guiding relationships and directing government. We go by "love" in the principle: love your neighbor as yourself, and charity.


    C-Clinical was not an act of compulsion, but the care one would have for family.


    Bottom line - we created this company to do what we love to do: life-changing medical research; and to dedicate our time, talents, and resources to those who need them.

  • 10 Days Ago

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Clinical Research Associate
  • San Diego State University Research Foundation
  • San Diego, CA TEMPORARY
  • Overview This position is open until filled with an initial application review to take place after August 30, 2023. The starting salary is $5,806.67 per month, non negotiable. Candidates must submit a...
  • 22 Days Ago

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Clinical Research Coordinator II
  • Headlands Research
  • San Diego, CA FULL_TIME
  • Overview Artemis Research is a leading principal investigator- and patient-focused clinical research company dedicated to advancing medical treatments. Established in 2008 by colleagues who bring more...
  • 4 Days Ago

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Clinical Research Coordinator I
  • Headlands Research
  • San Diego, CA FULL_TIME
  • Overview Artemis Research is a leading principal investigator- and patient-focused clinical research company dedicated to advancing medical treatments. Established in 2008 by colleagues who bring more...
  • 4 Days Ago

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PRN Clinical Trials Research Assistant
  • Headlands Research
  • Escondido, CA PER_DIEM
  • Overview The Headlands Research - AMCR Institute is dedicated to attracting, nurturing, and retaining patients and staff in order to carry out outstanding metabolic research. Our volunteers, sponsors,...
  • 24 Days Ago

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Clinical Research Coordinator - San Diego
  • Headlands Research
  • San Diego, CA FULL_TIME
  • Overview Artemis Research is a leading principal investigator- and patient-focused clinical research company dedicated to advancing medical treatments. Established in 2008 by colleagues who bring more...
  • 16 Days Ago

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0 Clinical Research Associate jobs found in Escondido, CA area

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Clinical Coordinator
  • Russell Tobin
  • San Diego, CA
  • Job Description Job Description The Scientific Team at Russell Tobin & Associates is supporting a world-class Medical De...
  • 3/28/2024 12:00:00 AM

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Clinical Affairs Manager - Remote
  • Danaher Corporation
  • San Diego, CA
  • Wondering what is within Beckman Coulter Diagnostics? Take a closer look. At first glance, you will see that for more th...
  • 3/28/2024 12:00:00 AM

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Clinical Dietician FT Days
  • Bay Area Hospital
  • San Diego, CA
  • Quick Submit $5,000 Sign-on Bonus Time Type: Full time Hours per Pay Period: 80 Shift: Day Shift 8-80 Average rate: $34....
  • 3/28/2024 12:00:00 AM

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Clinical Dietician FT Days
  • Bay Area Hospital
  • Chula Vista, CA
  • Quick Submit $5,000 Sign-on Bonus Time Type: Full time Hours per Pay Period: 80 Shift: Day Shift 8-80 Average rate: $34....
  • 3/28/2024 12:00:00 AM

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Clinical Research Associate (CRA)
  • LifeNet Health
  • San Diego, CA
  • Description Clinical Research Associate Location: San Diego, CA Department: Global Clinical Affairs Job Type: Full-Time ...
  • 3/27/2024 12:00:00 AM

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Clinical Trial Manager
  • ORIC Pharmaceuticals, Inc.
  • San Diego, CA
  • Description The Clinical Trial Manager (CTM) is responsible for the management of clinical trials from study start-up ac...
  • 3/27/2024 12:00:00 AM

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Clinical Documentation Specialist (Academic Medical Center Exp) - 100% Remote
  • Amerit Consulting
  • San Diego, CA
  • Overview: Our client, a Medical Center facility under the aegis of a California Public Ivy university and one of largest...
  • 3/26/2024 12:00:00 AM

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Clinical Research Coordinator
  • Topography Health
  • San Diego, CA
  • Topography Health is a first-of-its-kind, physician-focused clinical trials platform. We offer a full stack of tools and...
  • 3/25/2024 12:00:00 AM

According to the United States Census Bureau, the city has a total area of 37.0 square miles (96 km2). 36.8 square miles (95 km2) of it is land and 0.2 square miles (0.52 km2) of it is water. The total area is 0.48% water. The city is growing at a rapid rate with new communities like Hidden Trails appearing at the east end of East Valley Parkway. The city proper is surrounded by several sparsely populated unincorporated communities. These include Jesmond Dene and Hidden Meadows to the north; Felicita Park to the southwest; and Rincon Del Diablo to the southeast. Residents of these communities...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Research Associate jobs
$73,128 to $96,595
Escondido, California area prices
were up 2.6% from a year ago

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