Database Registration

Clinical research studies – Recruiting qualified, experienced research sites

At PMI, we have an ongoing interest in qualified, experienced research sites for both new and in-progress clinical trials in the following medical specialties and therapeutic areas:

    • Anesthesiology/respiratory therapy
    • Cardiovascular
    • Cosmetic
    • Dental
    • General/plastic surgery
    • Hematology
    • Homeopathy
    • Neurological
    • Nutrition
    • OB/GYN
    • Oncology
    • Ophthalmology
    • Orthopaedic
    • Otolaryngology
    • Peripheral/CNS

    Becoming involved with a contracted PMI study begins with registering in the PMI Study Site Database. This database is part of our review process for identifying clinical sites for potential studies and, at times, expansion of existing studies.

    If you are an experienced study site and would like to be considered for future studies, please complete our Study Site Information Form:

    We appreciate your interest in PMI! We offer a variety of clinical services to meet our clients’ needs, many of which are dependent on our relationships with qualified study sites. Please provide the information requested on this form. Your medical specialty, IRB requirements and clinical trial experience are key search criteria in our database. We look forward to receiving your completed form and associated Curriculum Vitae.

    *Indicates required information

    Selection Process
    The information you provide is reviewed by our proposal specialists and compared to the clinical study requirements of current and future studies. Important factors for consideration include therapeutic specialization, experience, patient population availability, geographic location, office/clinic/lab facilities, current studies in progress, and PMI’s previous study relationships, if applicable.

    If there is a potential match, your clinical site information will be reviewed with our client and confidentiality agreements will be completed. Our Clinical Services Department will then contact you to discuss the study parameters, protocol requirements, project timeline, and your resource availability. A qualification visit may be scheduled by either our Clinical Services Department or a client representative. Upon successful completion of these steps, a contract between your site and our client may be negotiated and completed.