Reporting Associate

Employer
Labcorp Drug Development
Location
Huntingdon, United Kingdom
Salary
Competitive
Start date
24 Jan 2023
Closing date
23 Feb 2023

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Discipline
R & D , Scientific
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)
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Job Details

At Labcorp we are committed to developing ourselves and our teams. We aim to create an environment that stimulates growth where you can achieve your fullest potential. This role is ideal for an aspiring life science graduate/professional looking for career development within a non lab based role.

This is an exciting opportunity for you to work as a Reporting Coordinator. In this role you will be working closely with Study Directors managing the full cycle of reporting. You will be working on many different animal studies and pulling/reporting the data.

The ideal candidate will have a science degree, as you will be needing to understand and translate the data you are working. Studies will be related to different animal studies. You will also be computer literate as you will be working on many different in-house systems.

Full training is provided and this is a hybrid role (home based, with occasion on-site Huntingdon visits).

Duties:

 The Reporting Associates I learns and performs the duties of drafting and finalizing nonclinical study reports and completes the following duties with limited supervision.

• General Duties
o Learns to and conducts contact with clients.
 Prepares form letters and communication text.
 Assists other client-facing staff (e.g., study director) with organizing client site visits and client conference calls
o Learns to and uses software tools to efficiently and accurately complete job duties. Types of software include word processing, spreadsheet, table generation, collaboration/sharing, and database applications.
o After completion of sufficient training, manages a full study workload with complex study designs by adhering to report preparation schedules and prioritizing tasks. Identifies and resolves changes to established study schedules to ensure client deliverables are met.
o After completion of sufficient training, begins to learn leadership within the reporting solutions group on activities such as performing peer reviews, preparing and delivering presentations, participating in staff meetings, participating in process improvement projects, and/or liaising with cross-site staff.
o After completion of sufficient training, may provide training and mentoring to new reporting associate staff members.
• Report Preparation
o Learns to and prepares the study report using details described in the protocol, protocol amendments, and study communications and Covance or client-specific requirements
o Learns to and incorporates contributions (e.g., protocol, protocol amendments, certificates of analysis, contributor reports) into the draft report
o Learns to and prints, binds, and mails draft and final study documents
o Learns to and addresses quality assurance inspection items on GLP-regulated studies
o Learns to and finalizes study reports and obtain, prepare, and deliver materials to archives
o Learns to and prepares report amendments
o Learns to and assists in the preparation of tabulated summaries in association with the study director
• Data Table Preparation
o Learns to and prepares data tables including completing basic statistical analysis in table generation programs.
o Learns to and drafts and quality checks data tables that were manually prepared
o Learns to and reviews data tables for accuracy
• Scheduling Responsibilities
o Learns to and reviews and adjusts the reporting schedule to ensure client expectations are met
o Learns to and schedules and leads the prewriting meeting, as required
o Learns to and schedules and coordinates study report finalization efforts
o Learns to coordinate expedited reporting, as necessary, among global counterparts

Education:

Science degree or relevant experience

Experience:

Computer literate

Strong attention to detail

Excellent multi-tasker

Labcorp is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, Labcorp strives for diversity and inclusion 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 of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), 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. We encourage all to apply.

For more information about how we collect and store your personal data, please see our Privacy Statement .

Company

At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions —because we know that knowledge has the potential to make life better for all. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations. Here, you can join our more than 70,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on people’s lives. Join us in our pursuit of answers.

 

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Find Us
Website
Mini-site
Labcorp Drug Development
Location
Maidenhead Office Park
Westacott Way
Littlewick Green
Maidenhead
SL6 3QH
GB
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