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Clinical Study Manager

  • ... Posted on: Mar 10, 2026
  • ... Talentmark
  • ... Amersfoort, null
  • ... Salary: Not Available
  • ... Full-time

Clinical Study Manager   

Job Title :

Clinical Study Manager

Job Type :

Full-time

Job Location :

Amersfoort null United States

Remote :

No

Jobcon Logo Job Description :

Are you an experienced clinical research professional looking for a role where you can lead complex studies from start to finish? We are seeking a Clinical Study Manager for the Early Life Clinical Evidence team within a Global Research & Innovation Center. This organization is a leading international nutrition and health organization, committed worldwide to science-driven innovations that support health and well-being.In this role, you will manage complex clinical studies from start-up to completion, ensuring compliance with GCP and regulatory requirements. You will lead multidisciplinary project teams, coordinate with external partners such as CROs and study sites, and report on study progress, resources, budgets, and timelines. You will also introduce new insights and drive operational improvements within the team. Requirements:Master’s or PhD in Life Sciences or related fieldExtensive experience in (international) clinical researchStrong knowledge of legislation and ICH-GCP guidelinesExcellent project management, leadership, and communication skillsProven ability to solve complex challenges creatively

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Jobcon Logo Position Details

Posted:

Mar 10, 2026

Reference Number:

25742_4381843945

Employment:

Full-time

Salary:

Not Available

City:

Amersfoort

Job Origin:

APPCAST_CPC

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Are you an experienced clinical research professional looking for a role where you can lead complex studies from start to finish? We are seeking a Clinical Study Manager for the Early Life Clinical Evidence team within a Global Research & Innovation Center. This organization is a leading international nutrition and health organization, committed worldwide to science-driven innovations that support health and well-being.In this role, you will manage complex clinical studies from start-up to completion, ensuring compliance with GCP and regulatory requirements. You will lead multidisciplinary project teams, coordinate with external partners such as CROs and study sites, and report on study progress, resources, budgets, and timelines. You will also introduce new insights and drive operational improvements within the team. Requirements:Master’s or PhD in Life Sciences or related fieldExtensive experience in (international) clinical researchStrong knowledge of legislation and ICH-GCP guidelinesExcellent project management, leadership, and communication skillsProven ability to solve complex challenges creatively

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