Technical Resources International, Inc
Medical Writer
Technical Resources International, Inc, Bethesda, Maryland, United States, 20817
Job Title
Medical Writer
Location
Bethesda, MD 20817 US (Primary)
Category
Medical Writing
Job Type
Full-Time
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.
Medical Writer
Location
Bethesda, MD 20817 US (Primary)
Category
Medical Writing
Job Type
Full-Time
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.