Document Review Specialist II
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Job Location:
Monthly Salary:
Posted on:
16 hours ago
Vacancies:
1 Vacancy
Job Summary
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob Description
Summarized Purpose:
Effectively reviews documents created within or outside of the company to ensure quality of a standard that meets or exceeds clients expectations. Documents include: regulatory submissions integrated clinical study reports serious adverse event narratives study protocols and publications. Ensures integrity of data in tables against source documents. Instructs others outside of the quality review group on the review process.
Essential Functions
- Reviews highly technical documents of all types created within or outside of the company to ensure quality standard that meets or exceeds clients expectations.
- Verifies scientific logic and clarity of the document by verifying data in tables against source documents checking for consistency according to current regulatory standards and guidelines.
- Edits for accuracy consistency and grammatical correctness
- Adjusts schedule to accommodate unexpected requests for priority review.
- Revises scientific language for usage flow clarity and audience appropriateness.
- Proactively queries authors to ensure compatibility with unique preferences and scientifically sound judgment
- Maintains communicates and applies knowledge of current guidelines templates and industry standards
Qualifications:
Education and Experience:
- Bachelors degree or equivalent and relevant formal academic / vocational qualification
- Previous experience that provides the knowledge skills and abilities to perform the job (comparable to 5 years).
Knowledge Skills and Abilities:
- Should have Quality Review experience of CSR Protocol ICF IB IND Modules and any other regulatory documents
- Capable of concentrating on the details of a document without losing sight of the overall objectives and intent of the documents message
- Good knowledge of the methods techniques and procedures of medical writing tasks
- Strong analytical ability
- Good working knowledge of medical terminology statistical concepts GCP guidelines (e.g. ICH) and requirement of the FDA and other international regulatory agencies
- Detail oriented thorough and methodical
- Proficient grammatical and communication skills both oral and written
- Good organizational and planning skills
- Proven ability to work effectively in a team environment
- Advanced computer literacy and expertise
- Good understanding of document management systems
- Capable of working well under pressure and remaining motivated
- Capable of working both independently and collaboratively with a team in a cross-cultural geographically dispersed environment
Required Experience:
IC
Key Skills
- DRG
- Acute Care
- Adobe Acrobat
- ICD-10
- Records Management
- Technical Writing
- Clinical Documentation Improvement
- Documentation Review
- Sharepoint
- cGMP
- Document Management Systems
- Document Management
About Company
Electron microscopes reveal hidden wonders that are smaller than the human eye can see. They fire electrons and create images, magnifying micrometer and nanometer structures by up to ten million times, providing a spectacular level of detail, even allowing researchers to view single a ... View more
