Clinical Trial Supply Associate
Description✓CK Clinical are recruiting for a Clinical Trial Supply Associate to join a small Global Pharmaceutical Company at their site based in Central London on a 12 month contract basis.
✓Clinical Trial Supply Associate Role:
✓To assist with the management of all activities associated with the supply of CTS [Clinical Trial Supplies - IMP, comparators, AMP, etc] to support the clients Clinical Trials
✓Liaise with external vendors before and during Clinical Study start to ensure all plans and outsourced activities are progressed in a timely manner to meet study timelines and to ensure appropriate output to meet study demand
✓Responsibilities will include to:
✓To assist with the management of all activities associated with the supply of CTS to support the clients current Clinical Trials.
✓Liaise with external vendors before and during Clinical Study start to ensure all plans and outsourced activities are progressed in a timely manner to meet study timelines and to ensure appropriate output to meet study demand.
✓Where required, act as the primary contact with external CTS vendors during the maintenance stage of a clinical trial.
✓With input from CTSM, take responsibility for CTS management during the maintenance phase of a clinical trial.
✓Your Background:
✓Experience of working with Clinical Research vendors in the EU and/or UK.
✓An understanding of EU and/or UK regulations/guidance pertaining to the supply of IMP in clinical trials.
✓Experience working with external Clinical Research/CTS vendors Experience of GxP requirements, specifically in relation to Clinical Trial Supplies.
✓Knowledge of EU and UK regulations concerning the supply and use of IMP in Clinical Trials.
✓Previous experience in a GMP environment or exposure to GxP principles.
✓Apply:
✓It is essential that applicants hold entitlement to work in the UK
✓Please quote job reference 55457 all correspondence Show more →
✓Clinical Trial Supply Associate Role:
✓To assist with the management of all activities associated with the supply of CTS [Clinical Trial Supplies - IMP, comparators, AMP, etc] to support the clients Clinical Trials
✓Liaise with external vendors before and during Clinical Study start to ensure all plans and outsourced activities are progressed in a timely manner to meet study timelines and to ensure appropriate output to meet study demand
✓Responsibilities will include to:
✓To assist with the management of all activities associated with the supply of CTS to support the clients current Clinical Trials.
✓Liaise with external vendors before and during Clinical Study start to ensure all plans and outsourced activities are progressed in a timely manner to meet study timelines and to ensure appropriate output to meet study demand.
✓Where required, act as the primary contact with external CTS vendors during the maintenance stage of a clinical trial.
✓With input from CTSM, take responsibility for CTS management during the maintenance phase of a clinical trial.
✓Your Background:
✓Experience of working with Clinical Research vendors in the EU and/or UK.
✓An understanding of EU and/or UK regulations/guidance pertaining to the supply of IMP in clinical trials.
✓Experience working with external Clinical Research/CTS vendors Experience of GxP requirements, specifically in relation to Clinical Trial Supplies.
✓Knowledge of EU and UK regulations concerning the supply and use of IMP in Clinical Trials.
✓Previous experience in a GMP environment or exposure to GxP principles.
✓Apply:
✓It is essential that applicants hold entitlement to work in the UK
✓Please quote job reference 55457 all correspondence Show more →