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Scientific Writer I

Please see Special Instructions for more details.

The Public Health Institute (PHI) is an independent, nonprofit organization dedicated to promoting health, well-being and quality of life for people throughout California, across the nation and around the world. As one of the largest and most comprehensive public health organizations in the nation, we are at the forefront of research and innovations to improve the efficacy of public health statewide, nationally and internationally. PHI was distinguished as one of the top 50 “Best Non-profit Organizations to Work For” by the Non-Profit Times in a national search.

Posting Details

Position Information

Posting Number #111-17-5
Classification Title Scientific Writer I
Position Title #111-17-5
Protocol Coordinator
Program Areas Research (Program/Project)
Position Summary

PHI is seeking a Protocol Coordinator for the Children’s Oncology Group (COG). This position is located in Monrovia, CA.

The Protocol Coordinator writes or edits concept proposals, research protocols, and other documents related to clinical trials. Additionally, the Protocol Coordinator manages review and approval processes of protocols during clinical trial preparation and modifications of active studies.

PHI Introduction

The Public Health Institute (PHI) is an independent, nonprofit organization dedicated to promoting health, well-being and quality of life for people throughout California, across the nation and around the world. As one of the largest and most comprehensive public health organizations in the nation, we are at the forefront of research and innovations to improve the efficacy of public health statewide, nationally and internationally. PHI was distinguished as one of the top 50 “Best Non-profit Organizations to Work For” by the Non-Profit Times in a national search.

Duties & Responsibilities

Duties & Responsibilities:

Coordinating Responsibilities

  • Works with physician/scientists to assist in writing, developing and producing final versions of clinical research protocols.
  • Designs therapy delivery maps as part of the protocol.
  • Enters protocol details and development events in ProCon the SDO study tracking application.
  • Communicates with physicians, (Study Chairs and Scientific Committee Chairs) and other cooperative groups (as required), responsible for developing completed protocols and coordinates communication between these groups to assure required timelines are met.
  • Acts as liaison with the Data Center, Study Committee and other cooperative groups (as required) in developing a research document that incorporates the clinical details needed to treat patients and the research elements to answer study questions.
  • Attends semi-annual Group meetings to participate in committee meetings for studies in the disease areas to which they are assigned.
  • Assists the Research Coordinator in the development of the Data and Specimen Submission Schedule to ensure the specific requirements of the protocols as determined by COG or Intergroup Study Committees, federal agencies and Group Operations Data Center are met.
  • Interacts with Clinical Research Associates, Research Coordinators, Data Managers and Database Administrators in study monitoring.
  • Collects information on reported problems regarding consistency and/or clarity in open protocols and works with the Study Chair to amend the document.
  • Coordinates the conversion of protocols, related documents and forms to PDF for Internet access.
  • Assists with other projects as needed.

Writing Responsibilities

  • According to the guidelines established by the SDO and in collaboration with COG investigators and statisticians, drafts informed consents, edits protocols and revises standard paragraphs for some protocol sections.
  • Develop and maintain lay language databases
  • Assists with other projects as needed.
    Minimum Qualifications

    Qualifications:

    To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required.

    • BS Degree in life sciences, or related field, MS preferred.
    • 2-3 years writing experience including protocols, grants, or other documents related to scientific research.
    • Ability to work independently as well as collaboratively with Group staff and investigators.
    • Knowledge of Microsoft Office applications with particular proficiency in Word, with the ability to learn new software, as needed.
    • Excellent written and oral communications skills, a service orientation and outstanding interpersonal skills are essential
    • Knowledge of medical terminology is required.
    • Clinical Research experience helpful.
    Compensation

    Compensation:

    This is an exempt position and the salary is commensurate with experience. PHI offers a generous benefits package including medical, dental, vision, short/long term disability insurance, life insurance, 403b (group retirement annuity) and partial subsidy of public transportation cost. For more information about PHI’s benefits, visit our benefits page here.

    Open Date 12/07/2017
    Close Date
    Open Until Filled Yes
    Location Monrovia
    CA

    Supplement Questions

    Required fields are indicated with an asterisk (*).

    1. * Do you have the required education?
      • Yes
      • No
    2. * Do you have the required years of experience?
      • Yes
      • No
    3. * Do you have the necessary skills to perform this position?
      • Yes
      • No

    Applicant Documents to Attach

    Required Documents
    1. Resume
    2. Cover Letter
    Optional Documents