Remote Senior Global Clinical Data Manager

Worldwide Clinical Trials

Raleigh (NC)

Remote

USD 79,000 - 157,000

Full time

4 days ago
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Job summary

Worldwide Clinical Trials is seeking a Senior Clinical Data Manager for a remote US role. You will lead end-to-end data management across multiple global studies, ensuring data quality and timely delivery.

You will create crucial documents, oversee data cleaning and database lock, and manage resources, timelines, and risks while mentoring team members. You will partner with sponsors and cross-functional teams, contribute to process improvements, and support audits and regulatory interactions as

Qualifications

  • Bachelor's degree or higher in biomedical sciences, life sciences, computer science, or a related discipline, or equivalent relevant experience.
  • Minimum of 5 years of experience in clinical data management or a related role within pharma/biotech/medical device industries.
  • Strong knowledge of clinical data management best practices and technologies.

Responsibilities

  • Lead end-to-end data management activities across multiple global projects from start-up to database lock and closeout.
  • Develop key data management documentation such as Data Management Plans and database specifications.
  • Oversee UAT, data cleaning, vendor reconciliation, and database lock activities for timely study delivery.
  • Allocate resources, monitor budgets and timelines, and escalate risks as needed.
  • Represent Data Management in sponsor and study meetings with technical input on progress and issues.
  • Mentor and train Data Management team members and contribute to process improvements.

Skills

Data management
Clinical trials
Communication
Leadership

Education

Bachelor's degree or higher in biomedical/life sciences or related field

Job description

Worldwide Clinical Trials is seeking a Senior Clinical Data Manager for a remote US role. You will lead end-to-end data management across multiple global studies, ensuring data quality and timely delivery.

You will create crucial documents, oversee data cleaning and database lock, and manage resources, timelines, and risks while mentoring team members. You will partner with sponsors and cross-functional teams, contribute to process improvements, and support audits and regulatory interactions as

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