Prime Clinical Research is a site network ready to help you get involved in clinical research! If you are a physician with your own practice and want to get involved in research but don’t know where to start, let us help. Our experienced team of clinical research professionals will support and guide you through the training and certification processes required to conduct clinical trials safely and successfully, including human research protections (HSP), Good Clinical Practice (GCP), and peer-to-peer training. After your training is complete, our team works to promote your research site and clinical expertise to pharmaceutical sponsors and CROs so you can begin conducting trials. If you have existing staff who want to participate in research, we train them. If you need research staff, our coordinators and nurses are happy to work with you.
Responsibilities:
- Protect the safety and welfare of all trial participants.
- Ensure that participants understand the potential risks, benefits, and extent of their participation in a trial.
- Conduct the trial in accordance with the protocol, SOPs, and ICH GCP.
- Assess and monitor subjects’ safety and wellbeing.
- Maintain appropriate documentation such as source records, all IRB-approved protocol and informed consent form (ICF) versions, and original signed ICFs.
- Ensure all staff conducting the trial have the necessary training and experience.
- Provide necessary medical treatment to patients as needed throughout the duration of the trial.
Requirements:
- Valid medical license (MD/DO)
Compensation:
Trial budgets vary widely depending on indication, number of patients enrolled, and scope of the protocol. Compensation will be mutually agreed upon prior to your participation in a study.