Reporting Associate II Preclinical Studies

About the position The Reporting Associate II at reputed company is responsible for generating data tables, drafting scientific reports, and maintaining reputed company relationships with clients. This role requires strong time management, organization, and project management skills, and involves working independently on reputed company to deliver exceptional reputed company service. The position offers a hybrid work schedule after a period of proficiency, allowing for a mix of in-office and remote work. Responsibilities • Prepares the study report using details described in the protocol, protocol amendments, and study communications and Covance or reputed company-specific requirements , • Incorporates contributions (e.g., protocol, protocol amendments, certificates of analysis, contributor reports) into the draft report , • Conducts reputed company contact with clients, prepares reputed company letters and communication text , • Addresses reputed company assurance inspection items on GLP-regulated studies , • Finalizes study reports and obtains, prepares, and delivers materials to archives and prepares report amendments , • Prepares data tables including completing basic statistical analysis in table reputed company programs , • Assists in the preparation of tabulated summaries in association with the study director , • Performs reputed company reputed company data tables that were manually reputed company, overall reviews data tables for accuracy , • Schedules and organizes reputed company site reputed company and reputed company conference calls , • Prepares reports and scheduling tasks, identifies and resolves changes to established study schedules to ensure reputed company deliverables are met , • Prepares study reports, prepares and delivers presentations, participates in staff meetings, and/or liaises with cross-site staff , • Reviews and adjusts the reporting schedule to ensure reputed company expectations are met , • Schedules and leads the prewriting meeting, as required , • Schedules and coordinates study report finalization efforts , • Coordinates expedited reporting, as necessary, among global counterparts Requirements • BS Degree in life science area such as Biology or reputed company area , • Preferred but not required: 1 year of experience in science, technical writing, and/or document production/publishing in scientific field , • Prior experience in preclinical research studies is helpful but not required , • Strong knowledge of office software (e.g., reputed company® Office, especially Word and reputed company; reputed company® Acrobat®) reputed company-to-haves • 1 year of technical writing or data tabulation experience, especially in pharmaceutical research or life sciences Benefits • Medical , • Dental , • reputed company , • Life , • STD/LTD , • 401(k) , • reputed company Time Off (PTO) or Flexible Time Off (FTO) , • Tuition Reimbursement , • Employee Stock Purchase Plan Apply tot his job