Site Management/Investigator Payments Services & Products

  1. Monitoring Trip Checklist 1/3/2018

    Efficiently and effectively manage your trip checklists to help ensure compliance during any clinical trial with iMedNet.

  2. Clinical Operations 3/4/2016

    Clinical operations are a critical component in all studies. SynteractHCR’s highly skilled staff is well-versed in clinical trial operations including implementing, monitoring and managing the clinical components of a study. From start-up to close-out, experienced clinical managers and clinical research associates (CRAs) oversee each study’s clinical processes to ensure proper planning, conduct, patient safety, and data quality, while fostering good communication between study sites and sponsor.

  3. Phase IIb-III Clinical Trials 5/29/2013

    With decades of experience in clinical trial design, INC Research/inVentiv Health offers a full range of clinical trial services including bioanalysis, biostatistics, data management, feasibility studies, global safety and pharmacovigilance, medical writing, project management, protocol and case report form design, quality assurance, regulatory affairs, risk management, site management, strategic planning, and study monitoring.

  4. Functional Outsourcing 8/28/2012

    As a Clinical Outsourcing provider, RDP Clinical offers a scalable resourcing model that provides a comprehensive Clinical Site Management and Monitoring function across multiple projects, therapeutic areas or entire clinical programs. 

  5. Panther-Clinical Trial Mgmt System (CTMS) 11/9/2011
    Panther CTMS is an end-to-end clinical trial management system that unifies the organization of data, document, and processes.
  6. Investigator Relations 6/24/2011
    Our professionals do more than just identify your investigators. They carefully assess each potential investigator based on the specific requirements of your study.
  7. Rescue Services

    Due to the complexity of clinical trials and the constant struggle to keep trials on schedule, Rho is often called on to resolve issues when processes don't go as planned.

  8. Clinical Project Management

    Setting high expectations and exceeding them
    For more than 30 years, Rho has helped pharmaceutical and biotechnology companies successfully lead their clinical research projects from initiation to closure. Our Project Managers have years of experience managing clinical trials and programs, including decentralized and virtual trials, in our therapeutic areas of expertise, including Neurology, Psychiatry, Analgesia, Rare Disease, and Infectious Disease and Vaccines. This experience has also given them broad knowledge of clinical research which helps to unify their trial teams and deliver results that are within the desired scope, timeline, and budget.

  9. Clinical Monitoring and Operations

    Strong site relationships and efficient study start-up
    Successful study execution requires more than just source data verification (SDV) and on-site clinical monitoring. Our clinical operations team ensures efficient study start-up, quick enrollment, and high quality execution at the site-level through extensive therapeutic and regulatory knowledge, solid training programs, and development of strong site relationships. Our clinical operations experts also have extensive experience designing and executing decentralized and virtual clinical trials.