Job Description
Job Description
Description
Assists in research projects involving direct patient care with adherence to established
protocols so that projects are carried out as directed by the Institutional Review Board (IRB).
Works within scope of practice to perform clinical procedures. Collaborates with physicians
and clinical/ancillary team members to ensure integrity of research study.
• Participates in research project planning to determine feasibility of protocol
implementation based on knowledge of institutional capabilities/limitations, therapy,
and/or population of interest.
• Collaborates with Principal Investigator (PI) to determine patient eligibility for
clinical trial, including documentation of criteria specified in the protocol.
• Ensures initial/ongoing consent process is performed and documented in
compliance with the US Food and Drug Administration (FDA), Good Clinical
Practice, institutional policies, sponsor requirements, Institutional Review Board
(IRB) and related applicable regulations, guidelines and policies.
• Participates in educating research subjects, families and healthcare team members
on research study specifics and significant new information arising during conduct
of trial.
• Performs clinical procedures including, but not limited to, vital signs, phlebotomy,
specimen collection, electrocardiograms, administration of investigational agent
(under PI supervision), IV placement, catheters and patient
assessment/questionnaire completion.
• Participates in related audit preparation and facilitation, including FDA, IRB and
related internal and external monitors and auditors.
• Evaluates disease response results and physical assessment data, in conjunction
with PI, to determine response per protocol.
• Collaborates with PI to organize all phases of grant process for submission to
funding agencies and to ensure adherence to clinical trial agreement/ study
budgets.
• Collaborates with PI to organize all phases of grant process for submission to
funding agencies and to ensure adherence to clinical trial agreement/ study
budgets.
• Performs related duties as required. All responsibilities noted here are considered
essential functions of the job under the Americans with Disabilities Act. Duties not
mentioned here, but considered related are not essential functions.
Qualifications
Graduate from an accredited School of Nursing. Bachelor’s Degree in Nursing,
preferred. Must be enrolled in an accredited BSN program within two (2) years and
obtain a BSN Degree within five (5) years of job entry date.
Current License to practice as a Registered Professional Nurse in New York State
required, plus specialized certifications as needed.
Job Roles and Responsibilities
Good Clinical Practice (GCP)
Fast Learner
Patient Follow-up
Site Qualification Visits (SQVs)
IRB Submission
Regulatory/Ethics Documentation Collection and Submission
Sample Processing
Communication
Study Start-Up
Company DescriptionAt Top Talent HQ, we take pride in being industry leaders dedicated to revolutionizing how companies connect with exceptional talent and how professionals shape their careers.
Our commitment to excellence drives us to create a dynamic platform that fosters meaningful connections and catalyzes professional growth. With a proven track record and a passion for success, we are your trusted partner on the journey to achieving your career objectives.
Company Description
At Top Talent HQ, we take pride in being industry leaders dedicated to revolutionizing how companies connect with exceptional talent and how professionals shape their careers.\r\n\r\nOur commitment to excellence drives us to create a dynamic platform that fosters meaningful connections and catalyzes professional growth. With a proven track record and a passion for success, we are your trusted partner on the journey to achieving your career objectives.