Clinical Study Assistant in Alameda, CA

  • Title: Clinical Study Assistant
  • Code: RCI-27329
  • Location: Alameda, CA 94502
  • Posted Date: 11/22/2022
  • Duration: 6 Months
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  Job Description

ONSITE ONLY IN ALAMEDA.

Summary:

  • Working on-site in Alameda, California.
  • This is not a remote position and relocation accommodation to East Bay, Northern California is not offered.
  • Preference for candidates who have clinical research and/or laboratory experience.

Duties:

  • Working on-site in Alameda, California.
  • This is not a remote position and relocation accommodation to East Bay, Northern California is not offered.
  • Member of the clinical team responsible for conducting device clinical trials Phase I-IV according to the Code of Federal Regulations and ICH GCP guidelines.
  • Responsible for assisting clinical staff in: planning and conducting clinical trials; clinical trial supply accountability and management; study document filing; entering data in source documents and case report forms including data cleanup; and determining study completion.
  • May participate in monitoring adherence to protocols and completion of monitoring reports.
  • 0-3 years experience level.

Major Responsibilities:

  • Assist clinical staff in planning, conducting clinical trials, and study completion.
  • Assist clinical staff in device accountability, prepare devices for clinical study use, clinical study supply ordering and management, and preparation and cleanup of clinical lab for study use.
  • Assist clinical staff in study document filing and archiving.
  • Assist in entering clinical study data in source documents and in case report forms, including data cleanup.

Education and Experience, You’ll Bring:

  • Associate Degree minimum required. Bachelor degree is preferred.
  • 0-3 years of experience in conducting clinical research or laboratory experience in biology or related field is required with an Associate degree. No previous experience is necessary with a Bachelor’s degree.
  • Maintain computer skills required to work efficiently
  • Familiarity working with electronic devices containing study data and transfer of study data to another medium.
  • Familiarity with Electronic Data Capture and Electronic Trial Master File systems
  • Maintain effective and meaningful communication within the clinical team and with research and development team to ensure the success of the clinical trial.


About Rangam:

Rangam Consultants is a minority, women-owned, disability workforce solutions global organization. Specialized in attracting and retaining talents globally for a rewarding career in IT, Engineering, Scientific, Clinical, Healthcare, Administrative, Finance, Business Management, and many more, while integrating veterans and individuals with disabilities into the workforce. Indeed, we connect career aspirants to relevant job opportunities, be it jobs in USA, UK, India, or Ireland. Also remote jobs, work-from-home jobs, or contract jobs in different verticals and industries.
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