Job Overview:
Responsible for reviewing clinical study reports patient safety narratives appendices informed consent forms clinical protocols and amendments to ensure documents are accurate consistent grammatically correct well written and logical by providing review comments and documentation to the Writer.
Summary of Responsibilities:
- Ensures consistency and accuracy of clinical study reports patient safety narratives appendices informed consent forms clinical protocols and amendments to source documents templates and client requirements.
- Completes reviews and checklists within given timelines.
- Collaborates with writers to discuss discrepancies omissions and errors.
- Understands the task to be completed and the budgeted hours.
- Participates in staff meetings client meetings and project team update meetings as appropriate.
- Reviews and assists in department template updates.
- Performs any other duties as assigned by Manager or Supervisor.
- And all other duties as needed or assigned
Qualifications (Minimum Required):
- Associate degree or Bachelor of Science/Arts (BS/BA) degree.
- Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
- Ability to understand and perform basic mathematical computations.
- Understanding of medical pharmacokinetic and statistical principles.
Experience (Minimum Required):
- 3 years of clinical research experience.
- Minimum 3 years of experience at Associate Medical QC Editor level.
- Must have excellent command of the English language both oral and written. This includes knowledge of standard editing and proofing conventions grammar sentence structure and style.
- Ability to efficiently use basic software (e.g. Word Excel PowerPoint).
Preferred Qualifications Include:
- High level of attention to detail and specifics.
- Knowledge of medical terminology preferred.
Physical Demands/Work Environment:
Learn more about our EEO & Accommodations request here.
Job Overview:Responsible for reviewing clinical study reports patient safety narratives appendices informed consent forms clinical protocols and amendments to ensure documents are accurate consistent grammatically correct well written and logical by providing review comments and documentation to the...
Job Overview:
Responsible for reviewing clinical study reports patient safety narratives appendices informed consent forms clinical protocols and amendments to ensure documents are accurate consistent grammatically correct well written and logical by providing review comments and documentation to the Writer.
Summary of Responsibilities:
- Ensures consistency and accuracy of clinical study reports patient safety narratives appendices informed consent forms clinical protocols and amendments to source documents templates and client requirements.
- Completes reviews and checklists within given timelines.
- Collaborates with writers to discuss discrepancies omissions and errors.
- Understands the task to be completed and the budgeted hours.
- Participates in staff meetings client meetings and project team update meetings as appropriate.
- Reviews and assists in department template updates.
- Performs any other duties as assigned by Manager or Supervisor.
- And all other duties as needed or assigned
Qualifications (Minimum Required):
- Associate degree or Bachelor of Science/Arts (BS/BA) degree.
- Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
- Ability to understand and perform basic mathematical computations.
- Understanding of medical pharmacokinetic and statistical principles.
Experience (Minimum Required):
- 3 years of clinical research experience.
- Minimum 3 years of experience at Associate Medical QC Editor level.
- Must have excellent command of the English language both oral and written. This includes knowledge of standard editing and proofing conventions grammar sentence structure and style.
- Ability to efficiently use basic software (e.g. Word Excel PowerPoint).
Preferred Qualifications Include:
- High level of attention to detail and specifics.
- Knowledge of medical terminology preferred.
Physical Demands/Work Environment:
Learn more about our EEO & Accommodations request here.
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