Snr Clin Trials Admin

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Job description

IP Specialist (Senior CTA) - Flexible UK location - Client Dedicated

At Labcorp we embrace everything that makes an employee unique. Everyone with skill and ambition can reach their potential and there has never been a better time to join our organisation.

We are working with a high profile Pharmaceutical partner in the search for an IP specialist.

This is a sponsor dedicated role, permanently employed by Labcorp

This role would appeal to someone with previous experience in IP management, perhaps at a large CRO / Pharm company or a Clinical Supplies organisation. To apply you must be eligible to work in the UK and comfortable working full time on a permanent basis.

Education/Qualifications:
* BSc degree level or equivalent experience
Experience:

* Experience in IP distribution /clinical research
* Previous experience in clinical research or logistic
* Knowledge of the statutory requirements of IPM management in the UK and ROI as defined by the EU Commission Directive 2030/94/EC, EU Commission, GMP, Annex 13, EU Clinical Trial Directive, UK legislation, ROI legislation, and ethical guidelines.
* Knowledge of and experience with GCP and other regulations in force; ability to learn and apply SOPs and quality control.
* Excellent interpersonal, communication and organisational skills.

* Other Information: * This role is afull time & permanent position to beemployed through Covance. For more information please contact Andy Smith at Covance on or mail