Principle Investigator Clause Samples
Principle Investigator. The Principle Investigator for the performance and supervision of the Sponsored Research shall be set forth in Schedule I attached hereto.
2.3.1. If for any reason the Principle Investigator cannot conduct or complete the Sponsored Research, UEC will appoint a successor, subject to the approval of the Sponsor. If the parties cannot agree on a successor, either party may terminate this Agreement by written notification to the other party of such, and neither party shall be liable for delay or default on performance of obligations to perform the Sponsored Research, provided, however, that the parties shall discuss and decide in good faith handling of unused Research Cost, if any.
Principle Investigator. The research will be supervised by ▇▇▇▇▇▇ ▇▇▇▇▇▇, M.D., Ph.
Principle Investigator. The Institution shall conduct and supervise the clinical trial in accordance with this Agreement through [Principle Investigator Name] (the “Principle Investigator”), who is an employee of the Institution. The Institution and the Principle Investigator shall perform the clinical trial entitled [protocol title] (the “Study”) as set forth in Protocol No. [protocol number] dated [date] which is attached hereto as Annex 1 in accordance with the Agreement and the Study.
Principle Investigator. ▇▇▇▇▇▇▇ ▇▇▇▇▇, will serve as Texas State’s primary contact for the details regarding programmatic questions as well as individual Task Orders.
Principle Investigator. The research will be supervised by ▇▇▇▇▇▇▇▇▇ ▇▇▇▇ Surani. If for any reason ▇▇▇▇▇▇▇▇▇ ▇▇▇▇▇▇ is unable to continue to serve as principle investigator, and a successor acceptable to both Institute and Sponsor is not available, this Agreement shall be terminated as mutually agreed.
Principle Investigator. ▇▇▇▇▇▇▇ ▇. ▇▇▇▇▇▇, MD Riverside University Health System – Department of Medicine Does serial ultrasonography assessment for extravascular lung water and IVC measurement affect outcomes in inpatient heart failure management? • We plan to enroll 400 people such as yourself or your family member in our study. • We will watch you or your family member while they are in the hospital and track them for 30 days after they leave to see if they return to the hospital. • We plan to keep this information protected in our computers for 5 years. • You are invited to take part in this research study because you are getting treatment for heart failure (also known as CHF). • You will not be paid any money. • This research is to find out if ultrasound can protect your kidneys during your heart failure treatment. • It is important that you understand the following before deciding to be part of this research o Reason for doing this research. o The possible ▇▇▇▇▇ and benefits. o What you will have to do if you decide to participate. • Please take your time to read the information to help you decide. • Please ask the study staff if there is anything that is not clear. • Please ask the study staff if you would like more information. • If you decide to take part in the study, you need to sign the ‘Agreement to Take Part Form’ • If you decide not to take part in this study, your current and future medical care will not be affected in any way. • Heart failure symptoms are caused by extra water in your body. • These symptoms are treated with medications to remove extra water. • These medications work by making your kidneys to make more urine. • One of the possible side effects of these medication is worsening kidney function. • These medications are adjusted based on your doctor’s experience and blood test results. • The reason for this study is to find out if additional ultrasound can help your doctor to make decisions, and prevent worsening kidney function. • What happens if you decide to participate in the study? o You will be randomly assigned to one of two study groups. ▪ Usual group: will receive the best care for your heart failure available. ▪ Ultrasound group: will receive ultrasound tests in addition to the usual care. • What happens if you say ‘No”? o You are free to say ‘No’. o Your decision will not affect your current and future medical care.
Principle Investigator. The research will be supervised by Dr.
