Ref No.

QUO00607

Location

US ~ Miami

Assistant Clinical Nurse Coordinator

Assistant Clinical Nurse Coordinator        

Company Overview

Our growing and successful business comprises of over 700 talented individuals globally, in an environment where everybody counts and is instrumental to our success. With state-of-the-art manufacturing and clinical facilities in the UK and USA, we deliver a full range of drug development solutions around the globe saving our clients both time and money.

People join Quotient Sciences because we are a respected member of the drug development world, specializing in delivering innovative solutions that integrate formulation development, real-time GMP manufacturing, and clinical testing. We pride ourselves on the quality of our services and our engaged culture. We are passionate about helping our customers get new medicines to market.

The Role

Due to growth and expansion, we have an exciting opportunity for an Assistant Clinical Nurse Coordinator to join the Screening Department. As an Assistant Clinical Nurse Coordinator, you will be responsible for the performance of screening activities for prospective research participants.

Other tasks and responsibilities will include:

  • Must be able to read and understand protocols and participate in protocol training meetings.
  • Assists with the recruitment and screening of prospective research candidates.
  • Explains research study and obtains proper informed consent.  Ensures consents are completed prior to the performance of any screening activities.
  • Obtains medical histories and documents findings according to SOPs and Good Clinical Practice.
  • Assists with the performance and/or scheduling of all screening procedures required by protocol.
  • Assists in obtaining clinical laboratory specimens and shipping to the appropriate laboratory as needed.
  • Reviews abnormal results of screening tests with the Investigators and alerts candidates of results which need further medical evaluation.    
  • Reviews completed screening charts for completeness and conformity with protocol requirements.  Reports and documents any clinical results or compliance issues which would lead to study exclusion.
  • Assists with other duties as assigned.                                    

The Candidate

The successful candidate will have an R.N or L.P.N with at least two years of clinical experience preferably in clinical research.  Ability to perform multiple tasks and prioritize effectively to meet required deadlines with excellent organizational skills and problem-solving abilities.

Other essential skills and experience are:

  • High attention to detail
  • Excellent communication and interpersonal skills
  • Fluent in English/Spanish.
  • Computer literate.

Company benefits:

In return, you will receive a competitive salary, a generous benefits package, excellent training, and development, as well as an exciting career within a fast-paced and dynamic business.

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