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Clindove

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. 

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.

It’s free! You will also be paid for your time, travel, and participation!

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!

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.

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.

All contracts are negotiated by our budget specialist with many years of negotiation experience.

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

  • 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

Refer a friend to Clindove Research and earn $50! Help your loved ones gain early access to medical treatments while contributing to important medical research. Fill out the form below, and we’ll reach out to your referral soon!