Clinical Research Coordinator

Clinical Research Coordinator

Company

We are building the future of healthcare, where many more life-changing therapies can reach those who need it most.

Together with the top pharmaceutical and biotech partners, we’re scaling a new model for the clinical trial site, where more physicians and their patients engage in cutting-edge research to develop and approve new therapies faster.

Through innovation and a unique technology-enabled service model, our team of expert scientists, engineers, entrepreneurs, physicians, nurses, and patient volunteers are paving the way towards this more caring and creative world.

We offer:

  • Interesting work and many opportunities for professional growth
  • Competitive salary, benefits, and other incentives

Job Description

We are looking for a dedicated, experienced, and innovation-driven Clinical Research Coordinator.

You will be responsible for study coordination, including study start-up, patient recruitment, backup support, and other duties.  You will work under the supervision of the Principal Investigator(s) while exercising excellent clinical judgment in patient monitoring and care.

 Responsibilities:

  • Serve as the primary contact to ensure appropriate communications, trial management, and meeting of timelines.
  • Coordinate the operational aspects of new and ongoing clinical trials at the site.
  • Maintain daily contact with the Principle Investigator(s) for recruitment activities, study start-up, and general daily communication.
  • Be responsible for the execution of the protocol and ensure that all staff working on any given protocol have been properly delegated by the Principal Investigator and adequately trained on the protocol.
  • Recruit and pre-screen patients
  • Maintain and submit IRB communications and regulatory documents.
  • Prepare other study materials such as informed consent documents, case report forms, enrollment logs, and drug/device accountability logs. 

Qualifications

  • At least three years of experience as a CRC.
  • Ability to check and document vital signs and EKG (ECG).
  • Solid understanding of medical procedures
  • Strong management, organizational, and communication skills
  • Ability to lift a minimum of 50 pounds.
  • Phlebotomy experience is a plus.
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