The SMR physician requirements for participation in clinical trials were developed to ensure success.
What Investigators Provide:
- Your Expertise: review potential studies to determine feasability, help build relationships.
- Your Patients: spend 5-10 minutes to “sell” the study to your patients; help keep them in the study once enrolled.
- Your Dedication: help ensure enrollment goals are met/exceeded, give study priority on your schedule, etc.
- Your Time: read protocol, attend kick-off meeting (often Fri/Sat), site initiation visits, review labs/ECG’s, etc.
If you would like to join the SMR Investigative Site Network, please contact Deb Bergevin at firstname.lastname@example.org or by calling 360.329.5220.