Do you have a passion for medicine? Are you interested in contributing to the advancement of medical research? If so, then we’re interested in speaking with you. Rochester Clinical Research has been Advancing Medicine and Changing Lives for over 2 decades. Many of the new medications you hear about in the news (vaccines such as: Meningitis, Ebola, Anthrax, etc.) at one point, came through our doors first and we couldn’t be more proud of that. At Rochester Clinical Research, we’ve created more than a place where people simply come to work Monday through Friday, we’ve created a family. We not only think of our employees as family, but our volunteers too.

If you think you’d be a good fit, check out our current opening(s) and fill out the form below. We’d love to talk further.

Registered Nurse – Clinical Research Coordinator

Rochester Clinical Research is currently seeking a full time (days) RN for a position as a Clinical Research Coordinator. The job involves leading 4-8 simultaneous research studies under the direction of the Clinical Investigator (MD). Job duties include:

  • Being the “expert” on your assigned trials. Responsible for set up, documentation, and logistics of your trials
  • Assisting other coordinators on their assigned trials
  • Performing and documenting study procedures according to good clinical practice and site procedures:
  • Administering informed consent to subjects
  • Reviewing and documenting inclusion and exclusion criteria
  • Reviewing and documenting subject’s medications and indications for use
  • Reviewing subject’s medical history with the MD or NP
  • Dispensing and accounting for study medications
  • Documenting and reporting adverse events and collecting information for the Investigator to review and assess
  • Performing vitals, EKG’s, and drawing labs according to the protocol
  • Communicating with the Sponsor Monitor to clarify protocol and other issues
  • Meeting with Sponsor Monitors at regularly scheduled visits
  • Maintaining the organization of study files
  • Ensuring all data queries are addressed in a timely fashion and minimizing queries whenever possible
  • Work towards a Certified Clinical Research Coordinator credential- available after 2 years of full time employment

Required Skills:

  • IV/phlebotomy skills
  • Hospital or clinical experience (2+ years)
  • Good clinical judgment
  • Attention to detail
  • Willing to learn new technology
  • Team oriented
  • Critical thinker
  • Problem solver
  • Strong communication skills
  • Ability to multi-task
  • Flexible
  • Organized
  • Ability to follow through

Job Type: Full-time

Experience:

  • Registered Nurse: 2 years minimum (Required)

Fill out the form below to be considered:

reCAPTCHA is required.