Our Specialties

Our Clinical Research Coordinators facilitate and manage the various aspects of clinical trials, ensuring adherence to study protocols, regulatory guidelines, and ethical standards. They collaborate with principal investigators, healthcare professionals, and study participants, overseeing tasks such as patient recruitment, informed consent processes, and data collection. Their role is crucial in maintaining the integrity and success of clinical research endeavors, ultimately contributing to advancements in medical knowledge and patient care.

Our Clinical Research Assistants support the execution of clinical trials by assisting in various administrative, organizational, and data management tasks. They coordinate participant recruitment efforts, maintain regulatory documentation, and facilitate communication among research team members. Their role is integral to the smooth operation of clinical research studies, contributing to the generation of valuable medical insights and advancements in healthcare.

Clinical Research Nurse Practitioners contribute by conducting patient assessments, managing protocol adherence, overseeing data collection, and ensuring the safety and ethical treatment of participants, combining clinical expertise with research acumen to advance medical knowledge and patient care. They play a key role in the design and implementation of clinical trials, often serving as principal investigators or working closely with them. Sage Insight Group works with highly skilled professionals who integrate advanced nursing knowledge with clinical research responsibilities.

Our Registered Nurses combine their nursing expertise with research responsibilities, playing a crucial role in the planning and execution of clinical trials. They contribute by assessing and monitoring study participants, ensuring compliance with research protocols, and collecting relevant data. Additionally, they collaborate with interdisciplinary teams, coordinate patient care, and provide essential support in maintaining the highest standards of patient safety and ethical conduct throughout the research process.

Physician Assistants contribute significantly to clinical research by applying their medical expertise and patient care skills to various aspects of research protocols. They actively participate in the planning and execution of clinical trials, conducting patient assessments, obtaining informed consent, and managing participant follow-up visits. Additionally, Physician Assistants may collaborate with research teams in data collection, analysis, and contribute valuable insights, playing a crucial role in advancing medical knowledge and improving patient outcomes through evidence-based practices.