Research Nurse Administrator

Weill Cornell Medical College

New York, NY

JOB DETAILS
SALARY
$161,200–$187,500 Per Year
SKILLS
Adverse Events, Affirmative Action, Analysis Skills, Basic Life Support (BLS), Cancer, Certified Medical Assistant, Clinical Nursing, Clinical Practices/Protocols, Clinical Research, Clinical Trial, Communication Skills, Contract Research Organization (CRO), Corrective Action, Detail Oriented, Diversity, Documentation, Epic Beacon (Oncology), Epic Systems, Establish Priorities, FDA (Food and Drug Administration), FDA Requirements, Federal Compliance Regulations, Federal Laws and Regulations, GCP (Good Clinical Practices), Genetics, HIPAA (Health Insurance Portability and Accountability Act), ICH Regulations, Identify Issues, Infection Control, Legal, Maintain Compliance, Maternal-Fetal Medicine, Medical Assistance, Mentoring, Microsoft Excel, Microsoft Office, Military, Multitasking, Nursing, Nursing Management, Oncology, Operations Research, Organizational Skills, Patient Care, People Management, Physical Demands, Presentation/Verbal Skills, Process Improvement, Quality Management, Registered Nurse (RN), Regulations, Regulatory Compliance, Rehabilitation Act, Research Administration, Research Nursing, Research Protocols, Research Skills, Society of Clinical Research Associates (SoCRA), Spreadsheets, Standard Operating Procedures (SOP), Team Building, Team Lead/Manager, Team Player, Treatment Plan, Word Processing, Writing Skills
LOCATION
New York, NY
POSTED
4 days ago

Title: Research Nurse Administrator

Location: Upper East Side

Org Unit: Maternal Fetal Medicine

Work Days:

Weekly Hours: 35.00

Exemption Status: Exempt

Salary Range: $161,200.00 - $187,500.00

  • As required under NYC Human Rights Law Int 1208-2018 - Salary range for this role when Hired for NYC Offices

Position Summary

Under general guidance, reports to the Associate Director of the CCTO and the Medical Director of the CCTO. The Research Nurse Administrator oversees the Research Nurse Unit in the Cancer Clinical Trials Office and is responsible for the day-to-day management of the Research Nurse Specialist and Medical Assistant across the Meyer Cancer Center (MCC).

Job Responsibilities

  • Serves as a central point person for nursing related matters and issues. Provides guidance on clinically related questions within research programs. Troubleshoots potential issues and facilitates smooth clinical study operations.
  • Recruit, train, and supervise Research Nurse Specialists and Medical Assistants to ensure compliance and efficiency.
  • Reviews and implements necessary nursing competencies. Ensures that nursing staff's licensure and certications are current as required by regulatory agencies.
  • Ensures that all clinical staff maintain good quality source documentation according to ICH-GCP guidelines and FDA regulations and HIPAA requirements.
  • In collaboration with the Associate Director, conducts workload assessments, implements, and evaluates optimization strategies to ensure adequate stafng for research programs.
  • Identifies, communicates, and aids in SOP development and establishment of guidelines and processes in an effort to improve efficiency and overall conduct of research programs.
  • Participate in institutional committees as MCC CCTO representative. Serve as clinical trial operations expert in clinical research policies and workflow, providing feedback on clinical research operations and staffing capabilities.
  • Participate in process improvement projects and provide clinical trial operations perspective and impact.
  • Collaborate with the Epic/Beacon build team members to ensure that study treatment plans are built in according to the protocol for newly activated and amended therapeutic protocols, as needed.
  • Provides direct patient care as needed to meet clinical research needs and precepts and mentors research personnel in related tasks.
  • Responsible for various aspects of study treatment protocols, as deemed necessary; educates participants; reports adverse events; monitors participants on studies.
  • Contributes to the implementation of research protocols and the clinical management of patients on protocol in compliance with federal regulations, GCP guidelines, and internal policies.
  • Ensures compliance with regulatory audits/inspections and/or interval reviews. Develops and recommends corrective action plan to address deficiencies identified.
  • Performs other related duties as assigned.

Education

  • Bachelor's of Science Degree in Nursing

Experience

6+ years of related clinical research nurse experience.

Oncology clinical research experience preferred.

Supervisory and management experience preferred.

Knowledge, Skills and Abilities

  • Strong knowledge in Food and Drug Administration (FDA) and Office for Human Research Protections (OHRP) regulations, and International Conference on Harmonization (ICH) Good Clinical Practice (GCP) guidelines.
  • Excellent oral and written communication skills
  • Ability to foster smooth communications and teamwork among clinical research faculty, fellows and staff as well as external organizations (sponsors and contract research organizations).
  • Proficiency in MS Office, specifically word processing (Word), spreadsheets (Excel) and database applications.
  • Demonstrated organizational skills and ability to pay close attention to detail.
  • Demonstrated critical thinking and analytical skills.
  • Demonstrated ability to multi-task and prioritize in a fast-paced environment.
  • Demonstrated ability to remain focus despite frequent interruptions.
  • Ability to treat confidential information with utmost discretion.
  • Demonstrated ability to exercise standards of professionalism, including appearance, presentation, and demeanor.
  • Demonstrated ability to work effectively in a collaborative manner with departmental faculty and staff, as well as other institutional representatives.
  • Ability to work both independently and as part of a team.

Licenses and Certifications

  • Current NY State Registered Nurse License & Registration.
  • BLS certification, issued by the American Heart Association.
  • Infection Control Certificate
  • Society of Clinical Research Associates (SoCRA) or Association of Clinical Research Professionals (ACRP) certification preferred.

Working Conditions/Physical Demands

Standard office work

Cornell welcomes students, faculty, and staff with diverse backgrounds from across the globe to pursue world-class education and career opportunities, to further the founding principle of "any person, any study." No person shall be denied employment on the basis of any legally protected status or subjected to prohibited discrimination involving, but not limited to, such factors as race, ethnic or national origin, citizenship and immigration status, color, sex, pregnancy or pregnancy-related conditions, age, creed, religion, actual or perceived disability (including persons associated with such a person), arrest and/or conviction record, military or veteran status, sexual orientation, gender expression and/or identity, an individual's genetic information, domestic violence victim status, familial status, marital status, or any other characteristic protected by applicable federal, state, or local law.

Cornell University embraces diversity in its workforce and seeks job candidates who will contribute to a climate that supports students, faculty, and staff of all identities and backgrounds. We hire based on merit, and encourage people from historically underrepresented and/or marginalized identities to apply. Consistent with federal law, Cornell engages in affirmative action in employment for qualified protected veterans as defined in the Vietnam Era Veterans' Readjustment Assistance Act (VEVRRA) and qualified individuals with disabilities under Section 503 of the Rehabilitation Act. We also recognize a lawful preference in employment practices for Native Americans living on or near Indian reservations in accordance with applicable law.

About the Company

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Weill Cornell Medical College