Clinical Trial Supply Specialist FSP

For our Client-one of the most prestigious Pharmaceutical company in the world-we are currently looking for a Clinical Trial Supply Specialist to join the Team of highly experienced Professionals in Shanghai, China.

By joining Parexel FSP you are gaining a chance to work with the most brilliant minds in the Industry. You will be rewarded with a fulltime permanent position, competitive base salary combined with an exceptional benefits package and numerous incentives as well a chance to progress within our international Organisation.

As a Clinical Trial Supply Specialist you will be tasked to: Be the main contact person to support country study team to communicate with global PTDS, local PT or third party vendor to ensure proper management of clinical supply from order to destruction in accordance with ICH-GCP, local GCP, GMP, Roche SOPs, regulations and requirements. Manage clinical supply third party vendor. Work with local PT for third party vendor selection, evaluation and inspection, if apply. Support country study team to coordinate local PT and global PTDS to ensure a smooth clinical study medication importation as per study timeline. Track and document goods receipt status at local depot. Coordinate with local PT and country study team to make sure the clinical study medication to be dispatched to the clinical study site per request. Track and document dispatch information and clinical study medication receipt at study site. Support country study team to purchase the commercial drug for clinical study used and coordinate with local PT to conduct additional labeling upon request within required timeline.

Work with third party vendor to manage the supply of commercial drug used for clinical trials and purchased outside of SRPL to meet with country study team's requirements. Oversight third party vendor's performance and compliance. Deliver related process and training to third party vendor if necessary. Qualifications

A successful candidate will come with a Life Science Degree. Experience working in clinical research industry as well as GC/GMP knowledge on clinical supply management are also essential requirements for this role.

We look forward to hearing from you!