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Results for tag: "Clinical Project Management"

Archiving Clinical Trial Documents - Understanding Regulatory Requirements for Paper and Electronic Records - Product Thumbnail Image

Archiving Clinical Trial Documents - Understanding Regulatory Requirements for Paper and Electronic Records

  • Training
  • 60 Minutes
  • Global
Middle East and Africa Medical Device and Diagnostics Contract Research Organization Market Forecast to 2028 - COVID-19 Impact and Regional Analysis By Type and Services - Product Thumbnail Image

Middle East and Africa Medical Device and Diagnostics Contract Research Organization Market Forecast to 2028 - COVID-19 Impact and Regional Analysis By Type and Services

  • Report
  • August 2021
  • 111 Pages
  • Middle East, Africa
From
Europe Medical Device and Diagnostics Contract Research Organization Market Forecast to 2028 - COVID-19 Impact and Regional Analysis By Type and Services - Product Thumbnail Image

Europe Medical Device and Diagnostics Contract Research Organization Market Forecast to 2028 - COVID-19 Impact and Regional Analysis By Type and Services

  • Report
  • August 2021
  • 139 Pages
  • Europe
From
Regulatory Perspectives of Clinical Project Management: Meeting FDA Requirements for Clinical Trials - Product Thumbnail Image

Regulatory Perspectives of Clinical Project Management: Meeting FDA Requirements for Clinical Trials

  • Training
  • 90 Minutes
  • Global
Clinical Regulatory Pack of 11 Webinars - Product Thumbnail Image

Clinical Regulatory Pack of 11 Webinars

  • Training
  • Global
Understanding and Interpreting the EMA Reflection Paper on GCP Compliance in Relation to Trial Master Files (paper and/or electronic) for Management, Audit and Inspection of Clinical Trials - Product Thumbnail Image

Understanding and Interpreting the EMA Reflection Paper on GCP Compliance in Relation to Trial Master Files (paper and/or electronic) for Management, Audit and Inspection of Clinical Trials

  • Training
  • 60 Minutes
  • Global
Managing the Trial Master File - Considerations for Moving to Electronic TMFs - Product Thumbnail Image

Managing the Trial Master File - Considerations for Moving to Electronic TMFs

  • Training
  • 60 Minutes
  • Global
An Overview of Risk Management and Risk Analysis Techniques in Clinical Trials - Product Thumbnail Image

An Overview of Risk Management and Risk Analysis Techniques in Clinical Trials

  • Training
  • 90 Minutes
  • Global
Regulatory Documentation for Clinical Trials - Product Thumbnail Image

Regulatory Documentation for Clinical Trials

  • Training
  • 60 Minutes
  • Global
Mitigate Fiscal Risks in Clinical Trials: Coverage Analysis, Budgeting and Billing Compliance - Product Thumbnail Image

Mitigate Fiscal Risks in Clinical Trials: Coverage Analysis, Budgeting and Billing Compliance

  • Training
  • 60 Minutes
  • Global
  • 10 Results (Page 1 of 1)
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Clinical Project Management (CPM) is a specialized field within biotechnology that focuses on the management of clinical trials. CPM professionals are responsible for the planning, coordination, and execution of clinical trials, ensuring that all aspects of the trial are conducted in accordance with applicable regulations and standards. CPM professionals also provide oversight of the data collection process, ensuring that data is collected accurately and efficiently. CPM is a critical component of the biotechnology industry, as it helps to ensure that clinical trials are conducted in a safe and effective manner. CPM professionals are also responsible for the development of protocols and procedures for clinical trials, as well as the management of budgets and timelines. Some companies in the Clinical Project Management market include Parexel, ICON, Syneos Health, PRA Health Sciences, and Quintiles. Show Less Read more