Study Coordinator - LCMS

Lab; Harrogate; On-site; GBP 60,000 - 80,000; Full time

Job summary

A leading drug development company in Harrogate seeks a Study Coordinator for its Bioanalysis department. The successful candidate will undertake routine checking of analytical data, coordinate study activities, and ensure compliance with regulatory guidelines. Applicants should have a scientific degree or relevant experience, along with excellent communication and multitasking skills. The role offers competitive salary and flexible working opportunities.

Benefits

Competitive salary

Comprehensive benefits package

Flexible working opportunities

Qualifications

• Scientific degree or relevant scientific industry experience.
• Writing reports or administrative experience is beneficial.
• Exceptional communication skills.

Responsibilities

• Coordinating activities of key client studies in compliance with GxP guidelines.
• Drafting study documentation and generating study data.
• Liaising with clients regarding study issues.

Skills

Attention to detail

Excellent communication skills

Ability to multitask

Writing reports

SAS knowledge/experience

Education

Scientific degree (Biochemistry, Chemistry, Biology, etc.)

Tools

Microsoft Office packages

Microsoft Project

Job description

Overview

Are you looking for an office-based scientific role? Do you have excellent communication skills and attention to detail? Are you looking for a role with training and career progression opportunities? Do you want to be a part of the world's leading drug development company?

At Labcorp in Harrogate, North Yorkshire we are looking to recruit a Study Coordinator to join our Bioanalysis department.

Responsibilities

This role is to undertake routine checking of analytical data and reports generated in Bioanalysis (LC-MS/MS). Develop an understanding of bioanalytical method validation and sample analysis. Responsible for coordinating the activities of routine and non-routine studies in a timely, efficient, and quality manner.

• Coordinating the activities of key client studies in compliance with GxP regulatory guidelines
• Working closely with Lead Scientists/Study Managers to support all phases of bioanalysis studies
• Drafting study documentation & generating study data
• Overseeing report production through finalization and archiving of data
• Liaising with clients regarding study issues and working as part of a larger team to ensure the study is completed in a timely manner

What we offer

• Competitive salary and a comprehensive benefits package, including health coverage and contributory pension
• Ability to work with a variety of different clients on wide ranging projects
• Flexible working and career development opportunities

Education

• Scientific degree (Biochemistry, Chemistry, Biology, Molecular Biology, Biomedical Sciences etc)
• OR relevant scientific industry experience

Experience

• Writing reports or administrative experience would be beneficial
• Excellent computing skills, including word processing and use of spreadsheets (e.g. Microsoft Office packages and Microsoft Project)
• Ability to multitask and prioritise workload, with excellent attention to detail
• Exceptional communication skills
• SAS knowledge/ experience is an advantageous as this will be used to prepare data.

Equal Opportunity

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.

How to apply

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