Job Title
Medical Writer
Location Bethesda, MD 20817 US (Primary)
Category Medical Writing
Job Type Full-Time
Salary Range 70,000.00-85,000.00/YEAR
Education Master's Degree
Travel None
Job Description
Prepares scientific and regulatory documents on behalf of government and private sector clients for submission to the Food and Drug Administration (FDA) (Investigational New Drug applications, annual reports, preclinical and clinical study reports, safety reports, and investigator's brochures).
Performs literature searches and/or prepares summaries of results.
Prepares meeting reports and proceedings, safety documents or data analysis.
Contributes to technical proposals and responds to technical questions.
Job Requirements
Superior writing skills that require moderate to minimal editing.
Knowledge of regulatory requirements for clinical studies.
Performs core tasks with moderate to minimal supervision.
Strong software skills to include Microsoft Office products and reference management software.
Excellent time management and multi-tasking skills.
Ability to analyze medical research data and review experimental protocols.
Meets expectations with regards to work product.
We are equal opportunity/affirmative action employers, committed to diversity in the workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status, or any other protected characteristic under state or local law.
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Location Bethesda, MD 20817 US (Primary)
Category Medical Writing
Job Type Full-Time
Salary Range 70,000.00-85,000.00/YEAR
Education Master's Degree
Travel None
Job Description
Prepares scientific and regulatory documents on behalf of government and private sector clients for submission to the Food and Drug Administration (FDA) (Investigational New Drug applications, annual reports, preclinical and clinical study reports, safety reports, and investigator's brochures).
Performs literature searches and/or prepares summaries of results.
Prepares meeting reports and proceedings, safety documents or data analysis.
Contributes to technical proposals and responds to technical questions.
Job Requirements
Superior writing skills that require moderate to minimal editing.
Knowledge of regulatory requirements for clinical studies.
Performs core tasks with moderate to minimal supervision.
Strong software skills to include Microsoft Office products and reference management software.
Excellent time management and multi-tasking skills.
Ability to analyze medical research data and review experimental protocols.
Meets expectations with regards to work product.
We are equal opportunity/affirmative action employers, committed to diversity in the workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status, or any other protected characteristic under state or local law.
#J-18808-Ljbffr