Reporting Associate II Preclinical Studies
About the position
The Reporting Associate II at Labcorp is responsible for generating data tables, drafting scientific reports, and maintaining professional relationships with clients. This role requires strong time management, organization, and project management skills, and involves working independently on projects to deliver exceptional client 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 client-specific requirements
,
• Incorporates contributions (e.g., protocol, protocol amendments, certificates of analysis, contributor reports) into the draft report
,
• Conducts direct contact with clients, prepares form letters and communication text
,
• Addresses quality 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 generation programs
,
• Assists in the preparation of tabulated summaries in association with the study director
,
• Performs quality check data tables that were manually prepared, overall reviews data tables for accuracy
,
• Schedules and organizes client site visits and client conference calls
,
• Prepares reports and scheduling tasks, identifies and resolves changes to established study schedules to ensure client 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 client 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 related 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., Microsoft® Office, especially Word and Excel; Adobe® Acrobat®)
Nice-to-haves
• 1 year of technical writing or data tabulation experience, especially in pharmaceutical research or life sciences
Benefits
• Medical
,
• Dental
,
• Vision
,
• Life
,
• STD/LTD
,
• 401(k)
,
• Paid Time Off (PTO) or Flexible Time Off (FTO)
,
• Tuition Reimbursement
,
• Employee Stock Purchase Plan
Apply Now
The Reporting Associate II at Labcorp is responsible for generating data tables, drafting scientific reports, and maintaining professional relationships with clients. This role requires strong time management, organization, and project management skills, and involves working independently on projects to deliver exceptional client 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 client-specific requirements
,
• Incorporates contributions (e.g., protocol, protocol amendments, certificates of analysis, contributor reports) into the draft report
,
• Conducts direct contact with clients, prepares form letters and communication text
,
• Addresses quality 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 generation programs
,
• Assists in the preparation of tabulated summaries in association with the study director
,
• Performs quality check data tables that were manually prepared, overall reviews data tables for accuracy
,
• Schedules and organizes client site visits and client conference calls
,
• Prepares reports and scheduling tasks, identifies and resolves changes to established study schedules to ensure client 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 client 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 related 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., Microsoft® Office, especially Word and Excel; Adobe® Acrobat®)
Nice-to-haves
• 1 year of technical writing or data tabulation experience, especially in pharmaceutical research or life sciences
Benefits
• Medical
,
• Dental
,
• Vision
,
• Life
,
• STD/LTD
,
• 401(k)
,
• Paid Time Off (PTO) or Flexible Time Off (FTO)
,
• Tuition Reimbursement
,
• Employee Stock Purchase Plan
Apply Now