Do you have a Bio Chemistry degree or a good level of experience in a Chemistry lab?

Have you got experience with generating scientific data, study plan drafting and / or archiving of data?

Have you got a proven track record of multi-tasking in a busy environment?

Labcorp is a leading global life sciences company. With a missionto improve health and improve lives, Labcorp delivers world-class diagnostic solutions, brings innovative medicines to patients faster and uses technology to improve the delivery of care.

Our Dose Analysis department in Huntingdon are recruiting for a Study Coordinator, to join our other Study Coordinators on an *initial* 12 month fixed term contract, to work alongside the team of Study Directors in the department.

To coordinate the activities of routine and non-routine studies in compliance with appropriate company standards and regulatory guidelines specified in the study plans, protocols, or work agreements.

This role would suit someone coming from a GLP Laboratory environment, or an admin based scientific role.

There is huge scope for progression in this role! The opportunity to manage others, train and develop others and progress up the internal grades is available for the right candidate. Alternatively, if you already have that experience as well then we want to hear from you!

Responsibilities will include:

• Drafting protocols, amendments and study schedules as appropriate using study outline or client supplied information.
  
• Reviewing study compliance against protocol, SOP and regulatory agency guidelines.
  
• Preparation of study schedules based on input from Study Director (SD)/Principal Investigator (PI).
  
• Scheduling and participating in client, pre-initiation and other study related meetings as required.
  
• Recording and distributing meeting minutes.
  
• Reviewing progress and study status against initial work plan.
  
• Maintaining well documented, organised and up-to-date study files including study schedule, protocol and correspondence.
  
• Aid in the report preparation, including tables and figures.
  
• Assisting in the development and maintenance of standard report/table formats as required.
  
• Assisting in interpreting and evaluating data for reports.
  
• Performing archiving of data.
  
• Participating in the review process for protocols/amendments and scientific reports.
  

Experience:

• Experience in data generation in GxP environment, or study plan drafting or archiving of data and reports is desirable.
  

We Offer:

• Labcorp Drug Development offers a comprehensive benefits package, including health cover and contributory pension.
  
• Our ongoing success offers team members unsurpassed growth and career development opportunities.
  
• As a global company we can support your development and career aspirations every step of the way.
  

Labcorp is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.

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