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Trial Manager

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Job Location drjobs

others - USA

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Job Description

Ridgefield, CT
Contract Duration: 12-36 months
Rate: Negotiable

Responsibilities:

  • Excellent employment opportunity for a Trial Manager in the Ridgefield, CT area. (Open to Remote)
  • Responsible for managing global Supply Chain activities in support of national and International phase I IV clinical trials, including Investigator Initiated Studies (IIS).
  • Ensures the timely provision of clinical supplies for assigned trials.
  • TM provides trial specific supply chain strategies and is primary point of contact to global Clinical Operations and Clinical Development on a study level.
  • TM is responsible leader of the CTSU trial team within the matrix structure, ensuring international cross-functional collaboration, and developing interfaces for all Supply Chain activities on the basis of business, regulatory and industry need.
  • TM ensures that all work is performed in a safe manner, and in conformance with US, EU, and German regulations.
  • Implements concepts for improvements in job related processes and organization.
  • Support TASCM to provide and support ideas of improvement in process and organization.
  • Drive the implementation of new systems, innovations, methods and working concepts to increase standardization and efficiency in supply chain.
  • Support TASCM to monitor key performance indicators to drive continuous improvement.
  • Initiates and completes complex duties in an efficient manner without supervision with consideration of economy and timelines.
  • Initiates and completes non-routine procedures independently.
  • Writes operating procedures / working instructions if applicable.

Experience:

  • Bachelors' Degree or Masters' Degree
  • Can work independently and in a team environment.
  • Demonstrates mentoring and coaching skills.
  • Communicates the teams work orally and in writing.
  • Exhibits ability to interpret complex project requirements, and associated regulations, and provides ability to interpret complex project requirements.
  • Required Skills: CLINICAL OPERATIONS, IIS, OPERATIONS, SUPPLY CHAIN, CLINICAL TRIALS
  • Additional Skills: COACHING, INTERNET INFORMATION SERVICES, MENTORING

Employment Type

Full Time

Company Industry

About Company

100 employees
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