Frequently asked questions
What is a clinical trial?
Clinical Trials rely on volunteers to develop and test new medical treatments and devices, demonstrating their safety and effectiveness for FDA pproval.
Are clinical trials safe?
Clinical trials undergo close oversight by pharmaceutical companies and the FDA to ensure strict adherence to established guidelines. Throughout the trial and follow-up period, your physician and research coordinator will carefully monitor volunteer health status information to ensure your safety and well-being.
Furthermore, every research study must be approved by an Independent Institutional Review Board (IRB) composed of experts from the medical and legal fields. This board is dedicated to ensuring the welfare of study volunteers and continues to oversee the study throughout the trial.
Does it cost anything to participate?
It’s free! You will also be paid for your time, travel, and participation!
Can i participate in a study even if I dont’t have insurance?
Yes! Insurance is NOT needed. Please refer your coworkers, friends, and family that may be interested in a study too!
What are the benefits for me
Help your patients by offering the newest treatment options at no cost!
Add an income stream as a principal or sub investigator.
Have fun with a change of pace!
See your research patients at your practice or our other locations!
Gain research experience for your CV for future opportunities to be a PI!
how do you coordinate a trial?
Clindove Research ensures all study procedures are carried out seamlessly, including subject consent, medical histories, ECGs, vitals, lab draws, and more. We also handle queries, monitor and audit visits as required by the FDA, oversee drug accountability, and manage the shipping of hazardous materials. To ensure efficient and accurate study documentation, we use eSource software.
How do you manage regulatory? Documentation?
Clindove Research handles the submission of necessary documents to the Institutional Review Board (IRB), implementing and documenting protocol training through SOPs, and maintaining ongoing regulatory compliance throughout the study’s lifecycle. Our state-of-the-art eRegulatory documentation software ensures efficient and accurate documentation.
How do you manage Contract and budgeting?
All contracts are negotiated by our budget specialist with many years of negotiation experience.
how is the accounting and payments done?
We use an electronic program for managing timely study payments to sponsors, vendors, physicians, and subjects, including visit stipends.
What Are Your Site’s Capabilities?
eSource and eRegulatory system, allowing study sponsors/CROs to have real-time access to all data and remote monitoring.
Advanced clinical trial management system
Remote monitoring enabled
Generally activated within 4 weeks of selection Text and email messaging to rapidly enroll subjects.
Recruitment specialist for faster enrollment Automated appointment reminders via text messaging
Comfortable and spacious waiting room
What Equipment Do You Have?
- In house Laboratory (w/CLIA waver)
- EKG
- Ambient Centrifuge
- Refrigerator
- -20C Freezer
- -80C Freezer
- 6 Full Sized Exam Rooms
- Double Locked Storage
No worries!
If you still have questions or need further assistance, feel free to reach out to us using the contact form below. We’re here to help!
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Earn $50 by Helping Others Access Early Medical Treatments
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