Our Client is an independently owned and operated company that works exclusively with clinical trial materials. The UK site provides secondary packaging (labeling and kitting) of any dosage form into plain packaging to ensure blinding of supplies for clinical trials, and storage and distribution of clinical materials for use in clinical trials. Their facility near Reading serves as the distribution hub for the packaged clinical trial materials to Europe and the rest of world.

They are now seeking a Project Coordinator to join their dynamic team. This position is a full-time permanent role and will be based near Reading, Berkshire.

Job Purpose

This position is responsible for providing the Project Management group with administrative support.

Key Areas of Responsibility

• Work with the Project Manager in initial study discussions with client regarding packaging designs and issues
• Work with the Project Manager in the interpretation and preparation of preliminary layout drawings and packaging samples in compliance with protocol for final clinical trial kit detail and design
• Work with the Project Manager to ensure the accuracy as to all calculations relative to strength and appropriateness of components, correctness of proportions and other details
• Work with the Project Manager in label text approval process by assuring that clients have approved all necessary text approvals
• Works with the Project Manager with the randomization approval process, including the processing of randomization codes for use in the labeling system and assuring that clients have approved all necessary randomizations
• Create mock-up kits for clients under the direction of a Project Manager.
• Create packaging samples under the direction of a Project Manager.
• Create check sheets for batch records under the direction of a Project Manager.
• Perform the batch record creation process, including the creation of packaging samples
• Assemble the appropriate forms into batch records
• Execute batch records as Batch Record Supervisor
• Create material specifications under the direction of a Project Manager
• Work with the Project Managers to meet any administrative needs such as filing, typing cover letters, copying, scanning, sending letters, creating Interoffice Requests, etc.

Qualifications and Experience

• Bachelor's degree or equivalent preferred
• Familiarity with cGMP
• Familiarity with the pharmaceutical industry
• Good reading and writing skills
• Good communication skills
• English literacy
• Excellent mathematical skills
• Computer literacy skills
• Attention to detail

In return our client is offering a competitive package for the successful Candidate including a basic salary of GBP28,000 - GBP30,000 per annum plus benefits.

Please send your C.V to Lorraine Roger, Director at Atom Recruitment Ltd.