About this job

Great opportunity for a talented Chemistry graduate or early career Scientist with excellent communication skills, or an experienced laboratory Scientist looking to move into a non-lab-based role.

This is an opportunity to work for an exciting bioanalytical company with state-of-the-art facilities, supporting and assisting Project Managers to carry out studies to GCP/GLP for a range of clients.

Key Responsibilities:

• Provide support and assistance to Project Managers, ensuring regulated studies are carried out to GLP/GCP standards
• Oversee GLP compliant pre-clinical bioanalytical studies, through to GCP compliant clinical bioanalysis, supporting clinical studies through phases I – IV
• Prepare Study Plans and Study Reports in line with the client requirements and in-house SOPs/templates, amend Study Plans where required, and carry out Quality Control (QC) checks on study documents
• Be an engaged team member of the team, actively contributing and flexibly supporting your team members

• Ensure schedule of study activities is kept up-to-date with relevant information, assist with data management activities and responses to audit findings and client comments

Essential Background and Preferred Experience:

• Degree in Chemistry or related subject, or relevant experience
• Excellent written and verbal communication skills
• Good computer literacy
• Ability to work well within a team and independently with minimum supervision
• Excellent time management skills and ability to work to tight deadlines
• Highly motivated and eager to get involved with new ideas and initiatives

For your work, you will be rewarded with an excellent salary, flexible working environment and a clear career path into a Study Director role.

Apply today to learn more about this position!

Key Words: bioanalysis, analytical chemistry, bioanalytical, study management, study coordinator, Study Director, GCP, GLP, Cheshire, Manchester, South Manchester, VRS8541PC.

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