MRM Customized Training


With over 20 years-experience in clinical research and regulatory expertise, MRM is uniquely positioned to provide customized training solutions for specific monitoring needs including:

  • Clinical trials
  • Investigator recruitment
  • Monitoring plan
  • Development of Reports, Protocols and CRF
  • SOP writing
  • Study specific educational materials
  • Project management.

In the field of Clinical Research, proper staff training is critical to a successful trial. MRM’s variety of e-learning options allows for effective time and cost management by providing a choice of topic-specific or comprehensive professional development and training.

MRM seminars and webinars are available for in-house training and can be customized to meet your company’s specific educational needs. From all-inclusive programs to single topic presentations, MRM’s offers different training options to suit your particular situation.

Utilizing Google classroom, your staff can access specific training through modules such as:

  • Good Clinical Practices & FDA Regulations (Drugs, Biologics, and Devices)
  • Human Subject Protections: IRBs, Informed Consent & Financial Disclosure
  • The Investigator Site: Coordinating a Clinical Trial
  • Monitoring Method: Responsibilities, Techniques, Critical Thinking & Site Management Monitoring Essential Documents: The Trial Master File & Investigator Study File
  • Securing Compliance & Writing Monitoring Reports

Because of their wide experience and ample knowledge base, MRM is also further able to customize training specific to your company’s needs. MRM’s signature program, Fundamentals of Clinical Research, can be brought directly to your organization to train Clinical Monitors to study start-up.

Become a MRM Training Partner with confidence that your employees will be receiving quality, up-to-date and cost-effective clinical research training. Please call 877-633-3322 for more details or contact us via:

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