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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
The Clinical Data Reviewer will work closely with the Data Manager or designee in order to have a comprehensive understanding of the trials supported and collaborate on the data cleaning and monitoring activities needed based on the Data Management Plan (DMP). Furthermore, the Clinical Data Reviewer must be able to identify effective ad hoc monitoring solutions in response to new or emergent scenarios while maintaining the quality and integrity of the data. Therefore, an ideal candidate will demonstrate a strong analytical and rigorous thought process. All changes to the clinical trial database are managed in line with the company’s quality management system and supported by the appropriate study documentation to guarantee compliance with regulatory authorities and/or the company’s Sponsors.
This position will interact daily with the Data Manager and Project Delivery resources of the company.
Remote, US Only
The Clinical Trial Manager (CTM) is an integral part of clinical trials activities and is responsible for ensuring the successful planning, implementation, and execution of contracted clinical monitoring activities. This role is functionally responsible for all clinical monitoring team members throughout the duration of the clinical trial; ensures clear, concise, and appropriate communication with internal and external stakeholders; prepares and maintains process documentation; and ensures compliance with ICH and GCP guidelines, SOPs, and other requirements.
The Clinical Research Associate is responsible for tracking and maintaining study specific non-CRF databases and administrating clinical research projects. This is accomplished by collecting documentation, site management, clinical contact, and reviewing CRF’s. The CRA is also responsible for maintaining relationships with investigators.
The Sr. Statistical Programmer provides experienced technical expertise to develop process methodology to meet internal and external clients’ needs. Plan and coordinate the development of integrated programming solutions serving the full spectrum of statistical programming needs. Duties include creating all datasets, tables, listings and figures according to the project specifications as well as coordinating quality control efforts and implementing all programming required for study/project completion. Provide technical expertise and leadership to the department.
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.