Program Clinical Data Management Strategic Lead

2 weeks ago


Uxbridge, United Kingdom Regeneron Full time
Job Description:

The Associate Director, Program Clinical Data Management Lead plays a crucial role in the success of our clinical data management programs. With a minimum of 12 years of experience in the biotechnology, pharmaceutical, or health-related industry, you will be responsible for leading and managing programs in Clinical Data Management (CDM). Your expertise in CDM will help ensure that our clinical research studies are conducted efficiently and effectively.

In this position, you will be responsible for maintaining an overview of clinical program status and issues, communicating progress, risks, and changes to quality, timelines, and budget. You will also review plans and provide CDM expertise during protocol design, study startup, and conduct phases of studies. Additionally, you will ensure consistency within the program, develop standard methodologies, and oversee CDM study budgets.

The estimated salary for this position is $**175,000 - $225,000 per year**, depending on location and experience. Our company offers a comprehensive benefits package, including health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees.

We are looking for a skilled professional with a Bachelor's degree in Mathematics, Science, or a related field. As a member of our team, you will have the opportunity to work on exciting projects and contribute to the growth and success of our organization.

Key Responsibilities:

  • Lead and manage programs in Clinical Data Management (CDM)
  • Maintain an overview of clinical program status and issues
  • Communicate progress, risks, and changes to quality, timelines, and budget
  • Review plans and provide CDM expertise during protocol design, study startup, and conduct phases of studies
  • Ensure consistency within the program and develop standard methodologies
  • Oversee CDM study budgets


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