Study Coordinator - Environmental Sciences

jobs24.co.uk; Eye; On-site; GBP 25,000 - 45,000; Full time

Job summary

An exciting opportunity awaits as a Study Coordinator in a dynamic environmental science team. In this role, you will be pivotal in coordinating various studies while ensuring compliance with Good Laboratory Practice (GLP) and regulatory guidelines. The position offers a chance to work closely with Study Directors, draft essential documentation, and liaise with clients to resolve study issues. This innovative firm values flexibility and career development, providing a competitive salary alongside a comprehensive benefits package, including health coverage and a contributory pension. If you have a strong interest in environmental science and possess exceptional communication skills, this role is perfect for you.

Benefits

Health Coverage

Contributory Pension

Flexible Working

Career Development Opportunities

Qualifications

• Degree in a scientific field or equivalent experience preferred.
• Experience with GLP, GCP guidelines is ideal.

Responsibilities

• Coordinate key client studies in compliance with regulatory guidelines.
• Draft study documentation and oversee report production.

Skills

Multitasking

Attention to Detail

Exceptional Communication Skills

Education

Degree Level (Scientific or English)

Equivalent Industry Experience

Tools

Microsoft Office (Word, Excel)

Job description

We are looking for a Study Coordinator to work in our environmental science team at our site in Eye, Suffolk. This is an exciting opportunity to join a knowledgeable and dynamic team where you will play an integral role in supporting the CPC Analytical group. You will coordinate the activities of a variety of routine and non-routine studies and will work in compliance with appropriate company standards, Good Laboratory Practice (GLP) and regulatory guidelines specified in the protocols governing the work in which you are involved in a timely, efficient and quality manner.

Responsibilities:

1. Coordinating the activities of key client studies in compliance with regulatory guidelines
2. Working closely with Study Directors to support all studies
3. Drafting study documentation & generating study data
4. Overseeing report production through finalization and archiving of data
5. Liaising with clients regarding study issues and working as part of a larger team to ensure the study is completed in a timely manner

Minimum Requirements:

1. Degree Level (Scientific or English degree is preferred) or equivalent industry experience
2. Environmental Science background or strong interest in this area
3. Ideally collating data, report writing and other administrative experience
4. Some knowledge of GLP, GCP guidelines, ideally having worked in a highly regulated environment
5. Excellent computing skills, including word processing and use of spreadsheets (e.g. Microsoft Office packages including Word and Excel)
6. Ability to multitask and prioritise workload, with excellent attention to detail
7. Exceptional communication skills

Labcorp is a leading global life sciences company that includes contract research and developmental services to the pharmaceutical, medical technology, crop protection and chemical industries.

Competitive salary and a comprehensive benefits package, including health coverage and contributory pension. Flexible working and career development opportunities.