Report Coordinator - Life Science Technical Writer

Covance Inc Located in: Salt Lake City,  Utah
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Covance Inc Biotechnology Jobs Pharmaceutical Careers
 

JOB DESCRIPTION

Covance Report Coordinator- Life Sciences

 

Covance's BioAnalytical team is looking for two Report Coordinators to join their team in Salt Lake City, UT.

Duties include documentation and generation of bioanalysis study reports, analysis results tables, and correspondence in a fast-paced, deadline-oriented environment. Candidates must be able to track the project status for multiple ongoing studies using a variety of software applications/databases and laboratory information management systems (LIMs). 

 

Additional Job duties include:
- Completes report production tasks with limited supervision.
- Preparing data tables including completing basic statistical analysis in table generation programs
- Preparing manually compiled data tables
- Preparing the study report using details described in the protocol and protocol
amendments and Covance or client-specific requirements
- Incorporating contributions (protocol, amendments, certificates of analysis, contributor reports) into the draft report
- Addressing quality assurance (QA) inspection items
- Printing, binding, and mailing draft and final study documents
- Preparing shipping paperwork for study documents
- Scheduling and coordinating study report finalization efforts
- Obtaining the data books and delivering the final report and data to archives at study finalization
- Preparing report amendments
- Able to manage a full study workload by adhering to report preparation schedules and prioritizing tasks.
- Identifies and resolves changes to established study schedules to ensure client deliverables are met.
- Works with complex or specialty study designs Is proficient in basic office software (e.g., Microsoft® Office Word and Excel, Adobe® Acrobat®).

 

 

 

Project Coordinator, Project Manager, laboratory, preclinical

  • Bachelor of Science (BS) degree in science or related field.
  • Experience may be substituted for education.
  • Ability to utilize word processing software, database, spreadsheet, and specialized software.
  • Skilled in concise writing. Writing should require little external review or edit.
  • Knowledge of grammar, punctuation, composition, and spelling.
  • Minimum of 2 years of study coordination experience.
  • Excellent communication, presentation, and interpersonal skills.
  • Excellent attention to detail.
  • Ability to prioritize and manage time.
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CRITICAL REQUIREMENTS

COMPANY INFORMATION

Covance Inc. is proud to be the only drug development company with a full range of research and development services—from lead optimization, to commercialization and life cycle management. Covance, headquartered in Princeton, NJ, is the drug development business of LabCorp with global operations in more than 30 countries.

JOB INFORMATION

Seniority Level:
Experienced - Not Management
Function:
  Medical Writing
Preferred Industry Background:
 
Managing a team of:
N/A
Required Travel:

Base Salary:
Confidential
Bonus:
Benefits:
Other Compensation: