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Clinical Research Coordinator (Local)

Clinical Research Coordinator (Local)

Hired by MatrixLos Angeles, CA
13 days ago
Job type
  • Temporary
Job description

Job Title : Clinical Research Coordinator

City : Los Angeles

State : CA

Job Type : Travel Contract

Discipline : Allied

Speciality : Clinical Research Coordinator

Facility Setting : Short Term Acute Care (STAC)

Accepting Locals per Radius Rule? Yes

Contract Length : weeks

Shifts : Days

Shift Details : Day x-Hour ( : - : )

Weekly Schedule : Hours

Certifications / Licenses :

  • Required : Associates Degree + years of experience as CRC year of experience in Oncology BLS Longevity in previous roles Interest in temp to perm
  • Preferred : Bachelors Degree SoCRA or ACRP Certification Phlebotomy Certified Medical Assistant Diploma

Mandatory Experience :

  • Duties and Responsibilities
  • Establishes and executes logistical aspects of clinical research projects to achieve project objectives, including project planning, projecting resource requirements, and developing systems to ensure protocol compliance and patient safety.
  • Coordinates administrative functions of research studies, including scheduling of patients for research visits, procedures and labs and completion and maintenance of consent forms, case report forms, SAE’s and source documents.
  • Responsible for screening and recruitment of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and supporting the informed consent process.
  • Responsible for accurate and timely data collection, documentation, entry and reporting, including resolution of queries from sponsors or regulatory entities.
  • Coordinates institutional, pharmaceutical and internal audits, including facilitating third party study monitoring and designs and implements needed corrective actions.
  • Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information; present this information at regular research staff meetings.
  • Responsible for timely submission of adverse events, serious adverse events, protocol deviations, and Safety Letters in accordance with local and federal guidelines.
  • Identifies quality and performance improvement opportunities and collaborates with staff in the development of action plans to improve quality.
  • Plans and coordinates strategies for increasing research participant enrollment, and / or improving clinical research efficiency as needed.
  • Provides technical support for the preparation of grant proposals, publications, presentations and special projects.
  • Provides assistance with research project budget development, including identifying and classifying routine care vs. research related care and provides assistance with research participant research billing and reconciliation.
  • Attend meetings and conferences related to research activities, including research staff meetings.
  • Participate in planning, workshops, evaluation meetings, and seminars, educational or administrative meetings as necessary or requested; Participates in training and education of new research personnel.

    • Get in Touch :

    We want to hear from you! If you think you'd be a good match, submit your resume and reach out to Lisa at () - to learn more.

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    Clinical Research Coordinator • Los Angeles, CA