MAGI 2025 is now complete. Thank you to all of those who supported the conference.
Please note, we will be moving away from an East and West event format to one in-person event each spring and one virtual event in the fall due to the ability for MAGI@home to meet the education and training needs of broader teams.
Registration is now open for MAGI@home. Click here to sign up!
Whether you are a clinical research novice or veteran, work with a study sponsor, research site or CRO, MAGI 2025 will offer best-in-class educational opportunities for all career levels in support of your continuing education and your professional growth and success.
Stay tuned for more details about our program and our distinguished faculty.
Learn the nuances of ensuring your site is optimized for conducting clinical trials by ensuring:
Explore field-tested, easily implemented negotiation tools and techniques that can help you maintain control, improve turnaround times, and reduce last-minute scrambles including:
Strengthen your research billing compliance development and program oversight by understanding:
Understand and ensure adherence to the regulations on research participant protections, including:
Master approaches to maintaining trial quality and effective tactics for protecting participant safety and data integrity, including:
Learn the nuances of ensuring your site is optimized for conducting clinical trials by ensuring:
Explore field-tested, easily implemented negotiation tools and techniques that can help you maintain control, improve turnaround times, and reduce last-minute scrambles including:
Strengthen your research billing compliance development and program oversight by understanding:
Understand and ensure adherence to the regulations on research participant protections, including:
Master approaches to maintaining trial quality and effective tactics for protecting participant safety and data integrity, including:
Learn the nuances of ensuring your site is optimized for conducting clinical trials by ensuring:
Explore field-tested, easily implemented negotiation tools and techniques that can help you maintain control, improve turnaround times, and reduce last-minute scrambles including:
Strengthen your research billing compliance development and program oversight by understanding:
Understand and ensure adherence to the regulations on research participant protections, including:
Master approaches to maintaining trial quality and effective tactics for protecting participant safety and data integrity, including:
The WCG Innovation Challenge is returning to Boston! Don’t miss the opportunity to participate in this fun — and valuable — challenge. Listen to research professionals present the inventive ideas they’ve come up with related to clinical trial site efficiency, increased performance or quality improvement.