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Clinical Trial Supply Management Manager, HYBRID

Job DescriptionJob Description

Job Title: Trial Manager

Duties: Tasks & Responsibilities -

  • You take over the responsibility for global Supply Chain activities for Investigational Medicinal Products (IMPs) of national and international clinical trials for Biological (NBE) projects.
  • In this role you act as the main point of contact to Clinical Development & Operations for assigned trials, ensuring the timely and cost efficient provision of clinical supplies.
  • With your comprehensive experience you will be the responsible leader of the CTSU trial team within the matrix structure, ensuring cross-functional collaboration and development of interfaces for all Supply Chain activities on the basis of business, regulatory and industry needs.
  • Thanks to your expertise you provide input to clinical trial protocols and bulk demands incl. comparator and non-IMP commercial products, to specific packaging designs and efficient distribution strategies.
  • Furthermore, you support investigations as Subject Matter Expert for assigned trials.

Skills: Requirements -

  • Bachelor's degree in natural sciences or similar disciplines or completed vocational training with several years' experience in clinical trials
  • Experience in working in an international environment, team leading and project management experiences as well as ability to interpret complex project requirements
  • Preferred is good knowledge and understanding of the regulatory and GMP/GCP requirements for IMPs
  • Strong problem solving capabilities with the willingness to make decisions and the ability to drive results
  • Very good communication, negotiation and presentation skills
  • Ability to work independently as well as in a team
  • Fluency in written and spoken English

Education:
Bachelors' Degree

Required Skills:

  • CLINICAL OPERATIONS
  • IIS
  • OPERATIONS
  • SUPPLY CHAIN
  • CLINICAL TRIALS

Additional Skills:

  • COACHING
  • INTERNET INFORMATION SERVICES
  • MENTORING

Company DescriptionMaxis Clinical Sciences provides complete Solution for Clinical and Digital Services. Maxis Clinical Sciences has been recognized in the industry for years, and an integrated research competence center. The company provides 24×7 delivery globally, with teams across the world’s 3 largest continents – North America, Europe and Asia. We operates with a problem-solving approach that believes in promoting genuine relationships & steady communication. It works as true clinical and digital competence center and provides services with 200 plus techno-functional, domain experts, each with 12+ years of average experience.

Our popular service niches that earned us global accolades are: clinical data management, clinical analytics, patient-centric technology enablement services, statistical analysis and reporting services, data anonymization services, RWD aggregation and curation services etc.Company DescriptionMaxis Clinical Sciences provides complete Solution for Clinical and Digital Services. Maxis Clinical Sciences has been recognized in the industry for years, and an integrated research competence center. The company provides 24×7 delivery globally, with teams across the world’s 3 largest continents – North America, Europe and Asia. We operates with a problem-solving approach that believes in promoting genuine relationships & steady communication. It works as true clinical and digital competence center and provides services with 200 plus techno-functional, domain experts, each with 12+ years of average experience.\r\n\r\nOur popular service niches that earned us global accolades are: clinical data management, clinical analytics, patient-centric technology enablement services, statistical analysis and reporting services, data anonymization services, RWD aggregation and curation services etc.]]>

Clinical Trial Supply Management Manager, HYBRID

Maxis Clinical Sciences
Ridgefield, CT 06877
Full time

Published on 01/30/2024

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