Posted 8 Nov 2026 (1 days ago) · Job 95001 · Read from the employer's Workday site, last checked 9 Nov 2026, 04:50 UTC

Reporting Associate

Labcorp · Huntingdon United Kingdom, United Kingdom

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Full time
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day

Work Schedule: 37,5h/week, Monday – Friday 8:30am-5pmfrom the posting

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Read the full posting as the employer wrote it

Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology and laboratory network, we advance diagnostics, accelerate innovation and help address some of the world’s most important health challenges. As we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. With our global scale and deep expertise, you’ll have the opportunity to do meaningful work, grow your career and make a real impact on people’s health around the world. Together, we’re improving health and improving lives.


Labcorp is seeking a Reporting Associate to join our Global Reporting Solutions team in Alconbury, Cambridgeshire.


Work Schedule: 37,5h/week, Monday – Friday 8:30am-5pm

This is a hybrid role (home based, with occasion on-site Huntingdon visits) where full training will be provided.

 

Job Responsibilities:

  • Drafting and finalizing nonclinical study reports
  • Using software tools to efficiently and accurately complete job duties. Types of software include word processing, spreadsheet, table generation, collaboration/sharing, and database applications
  • Preparing the study report using details described in the protocol
  • Incorporating contributions (e.g., protocol, protocol amendments, certificates of analysis, contributor reports) into the draft report
  • Addressing quality assurance inspection items on GLP-regulated studies
  • Drafting and quality checking data tables that were manually prepared
  • Reviewing data tables for accuracy
  • Client interaction
  • Managing a full study workload with complex study designs by adhering to report preparation schedules and prioritizing tasks

 

Minimum Qualifications:

  • BSc degree or relevant experience

 

Additional Job Standards:

  • Computer proficient with knowledge of office software e.g. Microsoft® Office, especially Word and Excel, Adobe® Acrobat®
  • Ability to work with and understand data
  • Strong attention to detail and accuracy
  • Team player
  • Excellent multi-tasker with the ability to remain organized and work to deadlines

 

Please note, due to the remote location of this site, there are no public transport links available.


Labcorp is proud to be an Equal Opportunity Employer:

Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. 


We encourage all to apply

If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Candidate_Accommodations@labcorp.com. For more information about how we collect and store your personal data, please see our Privacy Statement.


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