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Cognitive Research Corporation is continually looking to acquire exceptional talent. If you are considering a career move and have experience in the clinical research industry or career field indicated, then we are eager to speak with you and help you decide if CRC is the right fit.
At Cognitive Research Corporation, we pride ourselves on providing a vibrant professional climate for our team of valued employees. Our company culture prioritizes the mental health of our teams, and we understand that superior workers deserve superior work environments. That’s why we’re focused on supporting the mental health of our employees and maintaining a healthy work-life balance. If you’re ready to begin this exciting journey with us, please explore our open roles below.
Remote, US Only
Clinical Research Associate (CRA) is responsible for overseeing the execution of clinical trials at Investigative Sites. The CRA acts as a liaison between the study Sponsor, CRC and Investigative Sites. The CRA facilitates successful execution of studies by Investigative Sites and helps to ensure the rights, safety and welfare of human research participants as well as data integrity in clinical trials.
Remote, US Only
The Clinical Trial Manager (CTM) is responsible for the day-to-day leadership and management of monitoring services for clinical projects, including direct communication and interaction with clinical investigative sites, Clinical Research Associates (CRAs), and the project Sponsors. This role ensures that high quality monitoring services are delivered on-time and in compliance with International Conference on Harmonization (ICH), Good Clinical Practice (GCP) guidelines, Standard Operating Procedures (SOPs), and other requirements. The CTM is accountable for clinical monitoring team training, study specific tracking, project specific subject enrollment strategy and planning, CRA utilization and clinical monitoring process documentation.
Remote, US Only
The Medical Writer is responsible for the full scope of planning, writing, editing, and production of written research findings and regulatory documents. They are responsible for adherence to established regulatory standards, standard operating procedures (SOPs), client standards, and company and/or client-approved standards.
Remote, US Only
The PM is responsible for the overall project management of clinical studies. This is accomplished by ensuring all projects are completed on-time and on-budget while following all company policies and professional SOP’s and guidelines. The PM is also responsible for managing study staff and across department initiatives while maintaining client satisfaction.
We look forward to considering you for a role with the Cognitive Research Corporation team. Please complete the form below and we will be in touch soon.
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CRC is well-positioned to conduct clinical studies at any stage, Phase I-IV.