Medical Writer Asst

1) Implement and promote use of consistent, efficient and quality processes to meet timelines and deliverables according to requirements and standard operating procedures, and assume accountability for the deliverables 2) Ensure compliance of operations with governing regulatory requirements 3) Create, maintain and assume accountability for a culture of high customer service 4) Perform literature searches (clinical and non-clinical) and write non-clinical and clinical submission documents 5) Write parts of various safety reports for global regulatory submissions for Labcorp's clients, including Annual Reports (IND and other), Periodic Safety Update Reports, Periodic Adverse Drug Experience Reports, Bridging reports 6) Assist in writing Investigator brochures and sections of protocols 7) Assist in writing Clinical Study Reports for Ph 1-4 trials, including full study reports, abbreviated reports, web synopses 8) Assist pharmacovigilance teams in writing narratives for the adverse drug reactions and adverse events they process Labcorp is proud to be an Equal Opportunity Employer: As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status. For more information about how we collect and store your personal data, please see our Privacy Statement.