Clinical Research Nurse
Company: Prolerity Clinical Research
Location: Somers Point
Posted on: April 2, 2026
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Job Description:
The Clinical Research Nurse oversees the daily activities of
clinical research studies. They work closely with the clinical
teams and investigators to ensure that all required procedures and
visits occur according to protocol specific guidelines.
RESPONSIBILITIES Understand thoroughly all assigned studies through
reading protocols, attending investigator meetings and start-up
meetings, and coordinating with Principal Investigator Adhere
strictly to the study protocol; obtain exemptions when
necessary/appropriate Communicate protocol issues to CRO and/or
Sponsor, Site Administrator, Director, Principal or
Sub-Investigator Articulate all pertinent issues to the PI or
document by email/letter or during meetings Collect initial
psychiatric and medical information by interviewing patients and by
accessing other appropriate sources Ensure a flow of communication
including telephone conferences between patient, study staff,
referral sources, Sponsor and/or CRO, Monitor(s), Auditors and any
marketing groups hired by the Sponsor Utilize various rating scales
and maintain interrater reliability with other clinicians Perform
clinical tasks including, but not limited to, vital signs, height
and weight, ECG, phlebotomy, specimen packaging Maintain timely
source documentation as well as sponsor required information.
Dispense and maintain accurate records of study medication Educate
patients and family regarding their particular study and clinical
drug trials in general. Complete all monitor and sponsor queries in
a timely manner Provide appropriate community resource referrals to
patients, caretakers, and family at conclusion of patient’s
participation in study Requirements Ability to communicate clearly
and effectively (written and verbal) Ability to communicate in an
active multi-office environment Must possess excellent
interpersonal and customer service skills Ability to multi-task,
organize, prioritize appropriately, and work well both individually
and as part of a team Ability to use time productively and
contribute to high levels of company operational efficiency and
effectiveness Ability to maintain confidentiality of information
Ability to efficiently operate all job-related office equipment
(telephone, computer, calculator, fax, copier, study-specific
equipment) Required Experience Bachelor’s degree required RN
licensure Experience as a Clinical Research Coordinator (CRC) or
Research Assistant
Keywords: Prolerity Clinical Research, Newark , Clinical Research Nurse, Healthcare , Somers Point, New Jersey