Clinical Information Specialist


 

Responsibilities:

  • Abstracts protocol and/or contact/site/organization information into the appropriate databases for use by the client and their collaborators in support of clinical trials
  • Maintains data quality for protocol specific data and mastered level record
  • Responds to phone or email queries regarding standard processes associated with the abstractions
  • Uploads protocols and protocol-related documents to the appropriate Document Library and manages uploaded document.
  • Assists in the preparation of contract required reports
  • Takes notes at meetings and provides a summary of the meeting minutes to the client
  • Disseminates study information to required collaborators,
  • Stays current on relevant legislation and announcements regarding research
  • Participates in the revision/creation of SOPs, work instructions, and task specific manuals as necessary and appropriate
  • Handles special client requests as assigned
  • Works closely with offices both internal and external to ensure that data is properly conveyed and analyzed
  • Other duties as assigned

Requirements:

  • B.S. or B.A. degree or higher in Health Science or related fields, or equivalent related experience in clinical research.
  • Scientific or medical background preferred
  • Excellent oral, written, interpersonal, and organizational skills
  • Solid computer skills including Microsoft Office


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Job Snapshot

Employee Type

Full-Time

Location

Bethesda, MD (Onsite)

Job Type

Biotech

Experience

Not Specified

Date Posted

04/11/2023

Job ID

476/185/1119


 

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