Associate Study Coordinator - Metabolism

Labcorp; Harrogate; Hybrid; GBP 25,000 - 35,000; Full time

Job summary

A leading pharmaceutical company is seeking an Associate Study Coordinator to join their Metabolism team in Harrogate. This entry-level role offers an excellent opportunity for career progression and training while coordinating studies in compliance with regulatory standards. The ideal candidate will possess strong organizational skills and be proficient in Microsoft Office applications.

Benefits

Competitive salary

Comprehensive benefits package

Flexible working

Career development opportunities

Qualifications

• Relevant degree plus 4 years of experience (or equivalent experience).
• Some experience in regulated environments and knowledge of GCP and GLP guidelines is preferred.

Responsibilities

• Coordinating the activities of key client studies in compliance with regulatory guidelines.
• Working closely with Study Directors and drafting study documentation.
• Overseeing report production and ensuring timely completion of studies.

Skills

Organizational Skills

Attention to Detail

Communication Skills

Data Collation

Report Writing

Education

Relevant degree

Tools

Microsoft Office

Microsoft Project

Job description

Associate Study Coordinator - Metabolism

Labcorp Harrogate, England, United Kingdom

Get AI-powered advice on this job and more exclusive features.

Do you have fantastic organisational skills and want to work in the pharmaceutical industry supporting a growing Metabolism team?

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 Scientific Study Coordinator to join our in vivo Metabolism department.

The individual will have the responsibility for coordinating the activities of routine and non-routine studies for one business line in compliance with appropriate company standards and regulatory guidelines specified in the study plans, protocols, or work agreements governing the work in which they are involved in a timely, efficient and quality manner.

As a Study Coordinator Your Main Responsibilities Will Be

• Coordinating the activities of key client studies in compliance with regulatory guidelines
• Working closely with Study Directors to support all 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 Labcorp Can Offer You

• 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
  
  

Please note, this is a hybrid role that can include some home working upon completion of training.

Education

• Relevant degree plus 4 years of appropriate experience. Relevant experience may be substituted for academic qualifications
  
  

Experience

• Ideally collating data and writing reports or other administrative experience
• Some knowledge of GLP, GCP guidelines, ideally having worked in a highly regulated environment
• 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
  
  

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

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Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Analyst, and Information Technology

• Industries

  Hospitals and Health Care

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