Careers

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.

Join our growing team of experts and make an impact in this fast-paced industry.

Be proud of what you do.

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.

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Work where you're valued and appreciated.

Be supported.

  • 401(k) Profit Sharing Plan & Roth IRA
  • Comprehensive healthcare
  • Vacation + Flexible PTO
  • Flexible workplace to support work-life balance
  • Helping employees master their profession

Open Positions

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.

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Remote, US Only

The Senior Statistical Programmer provides experienced technical expertise to plan, track, and coordinate programming deliveries and the development of integrated programming solutions serving the full spectrum of statistical programming needs. Duties include creating datasets, Tables, Listings, and Figures (TLFs) according to the project specifications as well as coordinating quality control efforts and implementing all programming required for study/project completion. The Senior Statistical Programmer will also provide technical expertise and leadership to the department. This position will regularly collaborate with clinical operations and data management teams, as well as external partners and clients.

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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.

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Remote, US Only

The primary objective of this position is to ensure clinical study databases are built and validated to the highest quality standards to optimize data collection, data monitoring/cleaning, and efficient statistical analysis. They will lead the development and maintenance of clinical study databases developed internally for sponsored clinical studies and oversee activities of external database development. The Clinical Database Programmer will be looked upon to define, standardize, and implement best practices to improve quality and streamline data collection/cleaning efforts. The CDP will collaborate with internal and external stakeholders to identify, effectively communicate, and implement solutions to foster quality and timely execution of clinical study activities.

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St Petersburg, FL (On-site)

The Information Technology (IT) Support Technician provides set up, support and maintenance for desktop-based software applications, hardware configurations, and system analysis. The IT Support Technician provides assistance and support for integration between desktop and company applications, along with analyzing and documenting current systems and procedures. This role will assist with developing, documenting, and implementing standards and procedures to be used by IT staff and CRC employees, and supporting and completing projects as they relate to desktop and IT infrastructure.

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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.

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Remote with 20% travel to St. Petersburg, FL, US Only

The Senior Vice President of People and Culture will create and execute the overall strategy and programs to attract, develop, and retain the best talent. The ideal candidate will have a combination of strong Human Resources (HR), organizational development and business acumen skills, and a collaborative approach.

The Senior Vice President of People and Culture helps to operationalize people and culture initiatives and serves as a partner and advisor to the Executive Leadership Team regarding internal policies and processes (e.g., human resources, performance management, talent development and total rewards) to optimize employee engagement, productivity, retention, and to ensure employment law compliance.

Learn more and apply here!

Apply now!

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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