PHYSICIANS
AND INVESTIGATORS
Contribute to drug advancement and earn additional income through clinical research! Clindove Research is currently partnering with physicians in New York.
Expand Your Medical Career
Join Our Clinical Research Team
PRINCIPAL INVESTIGATOR (PI)
MD with expertise in the therapeutic area under investigation. The PI oversees the entire clinical trial, ensuring protocol adherence and participant safety.
CLINICAL/SITE INVESTIGATORS
MD with expertise in the therapeutic area under investigation. The PI oversees the entire clinical trial, ensuring protocol adherence and participant safety.
SUB-INVESTIGATOR
Assist the principal and clinical investigators in various aspects of the trial, contributing to participant management and data collection.
PHARMACOVIGILANCE SPECIALIST
Monitors and assesses the safety of investigational drugs, managing adverse event reporting and ensuring compliance with safety protocols.
CARDIOLOGIST
If the drug being tested has potential cardiovascular effects, a cardiologist may be involved to assess cardiac safety parameters.
ONCOLOGIST
Assist the principal and clinical investigators in various aspects of the trial, contributing to participant management and data collection.
NEUROLOGIST
For trials related to neurological conditions or drugs targeting the nervous system, a neurologist may be consulted.
INFECTIOUS DISEASE SPECIALIST
In trials related to infectious diseases or antimicrobial agents, an infectious disease specialist may be required.
DERMATOLOGIST
The medical specialty that deals with the study, diagnosis, and treatment of skin disorders and conditions of patients.
PEDIATRICS
Focusing on the medical care of infants, children, and adolescents, addressing their unique health needs and development.
PSYCHOLOGY
Studying the mind and behavior, exploring thoughts, emotions, and actions to understand and improve mental well-being and functioning.
OTHER SPECIALIST
Let’s connect. We want to add you to our list of MDs who are passionate about clinical research and drug trials.
Benefits
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!
Coordinating 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.
Managing 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.
Managing Contract & Budgeting
All contracts are negotiated by our budget specialist with many years of negotiation experience.
Accounting and Payments
We use an electronic program for managing timely study payments to sponsors, vendors, physicians, and subjects, including visit stipends.
Get Involved.
If you’re an investigator or physician let’s talk opportunities.
HOW TO PARTICIPATE
CONTACT US
Clindove Research is a local independently owned clinical research site in Brooklyn embedded in a multi specialty care clinic.