Biology Safety Assessment Reporting Associate Vacancy @ LabCorp
Do you have a passion for Science? Report Writing? Customer Relations? Accuracy? They have a great opportunity for a Reporting Associate in our Safety Assessment Department at their Madison, WI lab. Labcorp Drug Development’s work in developing new pharmaceutical solutions has an incredible impact on millions of lives worldwide. Be a part of this life-saving work and help improve patients’ lives while growing your career.
Job Title: Reporting Associate – Safety Assessment
Location Madison, Wisconsin, United States
Job ID: 77208
Eligibility Criteria:
Degree and/or experience in science (Biology, Animal Science, etc.), technical writing, and/or document production/publishing Work experience may be a substitute for education.
Strong oral and written communication skills
Experience:
- Basic knowledge of office software (e.g., Microsoft® Office, especially Word and Excel; Adobe® Acrobat®)
- Attention to detail, time management skills, and organizational skills
- Prefer at least 1 year of technical writing or data tabulation experience, especially in pharmaceutical research or life sciences.
Salary: They are offering a sign-on bonus of $3,000 ($1,500 upon hire and $1,500 after 6 months).
In this role, you will be responsible for generating data tables, drafting scientific reports, maintaining professional relationships with clients, communicating with internal staff, and working independently on projects. The ideal candidate will possess skills in time management, organization, and project management. As a Reporting Associate, you will utilize your scientific knowledge while working independently to deliver signature client service to our customers. Also, you will learn and perform the duties of drafting and finalizing nonclinical scientific study reports.
The Reporting Associate is responsible for communication between internal teams and clients, will coordinate and provide status updates to deliverables, generate data tables, draft scientific reports, and work independently on projects. Duties include but are not limited to:
- Drafts and prepares communication to the client and internal stakeholders including regular contact with clients
- Prepares and finalizes study reports according to study protocol, amendments and client-specific requirements
- Prepares complex data tables including the use of statistical analysis and table generation programs
- Addresses quality assurance inspection items on GLP-regulated studies
- Coordinates the study deliverables ensuring items are completed by prescribed timeline including coordination among global counterparts
- Identifies and resolves changes to established study schedules to ensure client deliverables are met
- Prepares final study documents; may print, bind and prepare for final delivery
- Prepares tabulated summaries in association with the study director
Schedules and leads prewriting meetings - In this position, you can apply your scientific knowledge from preclinical studies in preparing and coordinating of reporting and deliverables.
Biology Safety Assessment
