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Clinical Documentation Specialist - 9097050

Ascent

Job Description

Clinical Documentation Specialist
San Francisco, CA
6+ month contract

$22/hr
Assists in the coordination of documentation associated with conducting clinical studies. Assists CRAs and other clinical staff with management of trial master file documents, SOPs and record archiving. Supports the creation of standardized clinical trial tools, processes and SOPs.
  • Qualifications:
    Requires a minimum of a High School diploma.
  • An Associate's degree is a plus. Equivalent experience may be accepted. A minimum of 1 year industry experience working in the Pharmaceutical, Biotechnology or other related industry is highly preferred.
  • Strong attention to detail is a must.
  • Good communication skills both oral and written are a must. Good computer skills are required.
  • Working knowledge of MS Word, Excel, and PowerPoint is required. Excellent organizational skills are required. Must have an ability to multi-task.
Responsibilities:
  • Provides support to clinical research including, but not limited to, maintenance of documentation, clinical tracking and information retrieval.
  • Assists in management of access and organization of the controlled clinical document storage on-site at Nektar or third-party providers, including ensuring the defined file structure is maintained.
  • Assists with the exchange of TMF documents with external service providers. Maintains file QC schedule and perform periodic inventories of study/project TMFs to ensure completeness. Assists with off-site archiving activities (including budget, cataloguing process, and document retrieval).
  • Assists in coordinating communications, correspondence and associated documentation.
  • Performs duties such as, clinical form design, and filing of correspondence, lab reports, Clinical Monitoring Reports, and other study documents.
  • Assists with document retrieval.
  • Maintains and ensures all documentation are in a state of audit-readiness.
  • Assist in collection, dissemination, and/or tracking of regulatory documents as required. Performs all responsibilities in accordance with Standard Operating Procedures, established guidelines and work instructions, and appropriate industry and Good Clinical Practices standards.
  • Supports other projects as assigned. Performs other tasks as assigned.

Job Requirements

 
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Job Snapshot

Location US-CA-San Francisco
Employment Type Contractor
Pay Type Hour
Pay Rate $0.00 - $22.00 /Hour
Store Type Other

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Terms & Conditions
Snapshot
Ascent
Company:
US-CA-San Francisco
Location:
Contractor
Employment Type:
Hour
Pay Type:
$0.00 - $22.00 /Hour
Pay Rate:
Other
Store Type:

Job Description

Clinical Documentation Specialist
San Francisco, CA
6+ month contract

$22/hr
Assists in the coordination of documentation associated with conducting clinical studies. Assists CRAs and other clinical staff with management of trial master file documents, SOPs and record archiving. Supports the creation of standardized clinical trial tools, processes and SOPs.
  • Qualifications:
    Requires a minimum of a High School diploma.
  • An Associate's degree is a plus. Equivalent experience may be accepted. A minimum of 1 year industry experience working in the Pharmaceutical, Biotechnology or other related industry is highly preferred.
  • Strong attention to detail is a must.
  • Good communication skills both oral and written are a must. Good computer skills are required.
  • Working knowledge of MS Word, Excel, and PowerPoint is required. Excellent organizational skills are required. Must have an ability to multi-task.
Responsibilities:
  • Provides support to clinical research including, but not limited to, maintenance of documentation, clinical tracking and information retrieval.
  • Assists in management of access and organization of the controlled clinical document storage on-site at Nektar or third-party providers, including ensuring the defined file structure is maintained.
  • Assists with the exchange of TMF documents with external service providers. Maintains file QC schedule and perform periodic inventories of study/project TMFs to ensure completeness. Assists with off-site archiving activities (including budget, cataloguing process, and document retrieval).
  • Assists in coordinating communications, correspondence and associated documentation.
  • Performs duties such as, clinical form design, and filing of correspondence, lab reports, Clinical Monitoring Reports, and other study documents.
  • Assists with document retrieval.
  • Maintains and ensures all documentation are in a state of audit-readiness.
  • Assist in collection, dissemination, and/or tracking of regulatory documents as required. Performs all responsibilities in accordance with Standard Operating Procedures, established guidelines and work instructions, and appropriate industry and Good Clinical Practices standards.
  • Supports other projects as assigned. Performs other tasks as assigned.

Job Requirements

 
Clinical Documentation Specialist - 9097050 Apply now