Research Coordinator
Naval Medical Center San Diego - San Diego, CA

This job posting is no longer available on Naval Medical Center San Diego. Find similar jobs: Research Coordinator jobs

DESCRIPTION

Looking for an exciting new career? Join our team! The Geneva Foundation is a non-profit organization which promotes and supports military medicine. The Foundation has built relationships with highly skilled, exceptionally motivated, world-recognized researchers and medical professionals and hires top-quality staff. By joining The Geneva Foundation, you will have an exciting and stimulating career in which you will advance, "The Future of Military Medicine. Today."

The purpose of this study is to examine injury risk factors prospectively and retrospectively to determine if an abnormality in any one or a combination of factors identifies susceptibility to temporary threshold shift of hearing. Significant variability in individual susceptibility to noise-induced hearing loss has been reported without explanation. A retrospective-to-prospective review of audiometric data for a sample of listeners exposed to firing range noise while in a boot-camp environment, including relationships between known risk factors, has not yet been investigated.

A number of factors have been studied in humans that have indicated increased relative risk for hearing loss when exposed to hazardous levels of noise, when exposed to risk factors without noise, and when exposed to noise and non-noise factors. Investigators have attempted to identify levels of hearing loss susceptibility from these types of studies. This study will attempt to tie 2006 noise exposure for Marine Corps Recruit Depot students to their current state of hearing, using a review of health history information and hearing history data to populate a case-control analysis.

DUTIES

Duties include but not limited to:
  • Administer and conduct the daily operation of the clinical investigation including scheduling; supply and equipment needs, maintenance and oversight; study personnel oversight; and subject recruitment strategy and execution.
  • Provide coordination of investigators with study site personnel.
  • Create Standard Operating Procedures (SOPs) for and maintain oversight and responsibility for all study data collection processes as outlined in IRB approved protocols, including archiving and file management.
  • Assist the principle investigators with assorted administrative tasks as needed.
  • Responsible for all study approval submissions and processes.
  • Adhere to legal, professional and ethical codes with respect to confidentiality and privacy.
  • Responsible for explaining research protocols and obtaining signed consent from patients and research trial candidates as required per protocol.
  • Assist investigators as needed with construction and maintenance of study databases and study data collection forms, and data entry tasks.
  • Responsible for writing and submitting any written reports to study sponsor, IRB, investigators or study site Commands as required.
  • Ensure compliance with subject consenting and reporting of adverse events and side effects.
  • Track the expenditures for all study-related activities, including supplies and equipment.
  • Provide inputs to final reports that document the research findings for human use protocols including, but not limited to those listed above.
QUALIFICATIONS

  • Bachelor's Degree required
  • Minimum of 1 year experience as a lead Clinical Research Coordinator
  • Minimum of 5 years of experience working in clinical research environment.
  • Must be well experienced with Microsoft Word, Excel and PowerPoint Software.
  • Experience with monitoring and recording physiological data a plus.
  • Must have working knowledge of research data collection and records maintenance.
  • Must have experience in clinical research processes: reviewing case reports, coordinating the flow of information between case workers, IRB, medical monitor and principal investigator, handling case report forms in a secure manner and be certified under the HIPPA regulations regarding patient information.
  • Must have HIPAA, ICH, and GCP Certification and be competent in FDA regulations and processes, IRB applications and review processes, financial disclosure regulations, protocol design and development, clinical trial management and monitoring, and Adverse Event protocol.
  • Must possess current certification in American Heart Association (AHA) Basic Life Support (BLS) for Health Care Providers or American Red Cross (ARC) Cardio Pulmonary Resuscitation (CPR) for the Professional Rescuer.
  • Must have good oral and written communication skills, computer skills and experience with physiologic data collection software.
Knowledge of CHCS and AHLTA a plus.
  • Must have knowledge of record keeping practices specific to a Biomechanics lab and human subject confidentiality and of medical terminology to include but not limited to audiology.
Duties include but not limited to:
  • Administer and conduct the daily operation of the clinical investigation including scheduling; supply and equipment needs, maintenance and oversight; study personnel oversight; and subject recruitment strategy and execution.
  • Provide coordination of investigators with study site personnel.
  • Create Standard Operating Procedures (SOPs) for and maintain oversight and responsibility for all study data collection processes as outlined in IRB approved protocols, including archiving and file management.
  • Assist the principle investigators with assorted administrative tasks as needed.
  • Responsible for all study approval submissions and processes.
  • Adhere to legal, professional and ethical codes with respect to confidentiality and privacy.
  • Responsible for explaining research protocols and obtaining signed consent from patients and research trial candidates as required per protocol.
  • Assist investigators as needed with construction and maintenance of study databases and study data collection forms, and data entry tasks.
  • Responsible for writing and submitting any written reports to study sponsor, IRB, investigators or study site Commands as required.
  • Ensure compliance with subject consenting and reporting of adverse events and side effects.
  • Track the expenditures for all study-related activities, including supplies and equipment.
  • Provide inputs to final reports that document the research findings for human use protocols including, but not limited to those listed above.

Naval Medical Center San Diego - 19 months ago - save job - copy to clipboard - block
Recommended Jobs
Scientist 1
Illumina, Inc. - San Diego, CA
Illumina, Inc. - 7 days ago

Prospect Research & Database Coordinator
Sanford-Burnham Medical Research Institute - La Jolla, CA
Sanford-Burnham Medical Research Institute - 7 days ago

Veterinary Assistant, Technicians & More Need...
Banfield Pet Hospital - San Diego, CA
WhereTechsConnect.com - 3 days ago
About this company
7,983 reviews
The US Navy maintains a variety of military equipment like ballistic missile submarines, aircraft carriers, surface warships, attack...