Customized Clinical Trial Research Training
There is a significant need for the growth and development of skills and knowledge within the biopharmaceutical and medical device industries. Halloran offers customized research training courses that will help develop your people in the areas of Clinical Research Management. We customize our courses based on the needs of our clients.
Halloran conducts a needs assessment to identify and/or verify the specific needs of the client. We work with your team to fully understand both the experience level of the participants as well as identify the most pressing issues impacting performance. The result of the needs assessment is a customized course based on the top priorities of your company. Through the use of tailored case studies and focused group activities, we facilitate discussions to maximize the team’s performance to reduce issues with effective execution of your clinical trials.
Examples of Comprehensive Programs:
Examples of Short Courses:
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Protecting Human Subjects (2-4 hours)
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The Basics of Informed Consent (2 hours)
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Regulatory Document Workshop (4 hours)
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Fraud and Non-compliance in Clinical Research (2-4 hours)
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Preparing for Compliance Audits: The Research Site Perspective (2 hours)
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Finding the Best Research (2 hours)
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Technical Writing in Clinical Research (4 hours)
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Creating a Patient Recruitment Plan (2 hours)
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The Basics of Data Management (2 hours)
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Investigator INDs: Responsibilities and Practicalities for the Sponsor (2 hours)
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Emerging Trends in New Product Development for Senior Leadership (1-2 hours)