Clinical Research Nursing Lead

Wilmington, DE - USA

Monthly Salary: Not Disclosed

Posted on: 5 hours ago

Vacancies: 1 Vacancy

Job Summary

Description

The Lead Clinical Research Nurse will provide technical guidance and subject matter expertise to facilitate the coordination and conduct of clinical research studies and/or clinical trials within the department/division/unit within Nemours. This individual will play a key role by helping to coordinate implement and complete clinical research studies and/or clinical trials. Provides oversight training education to research staff. participates in continuous improvement projects and the development and implementation of standard operating procedures. Conducts meetings with Clinical Trials Management and Clinical Research Administration to discuss Key Performance Indicators and clinical trials budgets within the department/division/unit they are working addition the Lead Clinical Research Coordinator will supervise and develop Clinical Research team members within the department. This position will report to the Clinical Trials Manager.

Essential Functions:

Perform routine operational activities for multiple research protocols.
Assist with hiring training and oversight of research staff.
Conducts performance appraisals for direct reports in collaboration with Principal Investigators and Clinical Trials Manager according to Nemours expectations on an annual basis.
Develop and sustain a close working relationship with the studies Principal Investigators (PIs) including regular meetings to discuss projects issues recruitment consenting study execution specimen collection specimen processing specimen shipping and potential adverse events.
Liaise between site research personnel industry sponsors PIs and Supervisor and clinical departments.
Collaborate closely with various site departments/teams including finance relevant Nemours administrative representatives and the local IRB if applicable
Coordinate schedule of assessments from initial submission of feasibility until study closeout
Provide awareness of research protocols to appropriate site-level personnel including physicians nurses clinical staff and administrators
Document all specific tasks required by the protocol (i.e. medication forms quality of life questionnaires neuro exams vital signs sheets times of lab draws etc.)
Document all patient staff and sponsor correspondence including follow-up encounters adverse events interventions pharmacy dispensations and patient phone calls.

Requirements:

Bachelor of Science in Nursing
Active Delaware Nursing License
Active SOCRA or ACRP certification
American Heart Association BLS Certification

DescriptionThe Lead Clinical Research Nurse will provide technical guidance and subject matter expertise to facilitate the coordination and conduct of clinical research studies and/or clinical trials within the department/division/unit within Nemours. This individual will play a key role by helping ...

Description

Essential Functions:

Perform routine operational activities for multiple research protocols.
Assist with hiring training and oversight of research staff.
Conducts performance appraisals for direct reports in collaboration with Principal Investigators and Clinical Trials Manager according to Nemours expectations on an annual basis.
Develop and sustain a close working relationship with the studies Principal Investigators (PIs) including regular meetings to discuss projects issues recruitment consenting study execution specimen collection specimen processing specimen shipping and potential adverse events.
Liaise between site research personnel industry sponsors PIs and Supervisor and clinical departments.
Collaborate closely with various site departments/teams including finance relevant Nemours administrative representatives and the local IRB if applicable
Coordinate schedule of assessments from initial submission of feasibility until study closeout
Provide awareness of research protocols to appropriate site-level personnel including physicians nurses clinical staff and administrators
Document all specific tasks required by the protocol (i.e. medication forms quality of life questionnaires neuro exams vital signs sheets times of lab draws etc.)
Document all patient staff and sponsor correspondence including follow-up encounters adverse events interventions pharmacy dispensations and patient phone calls.

Requirements:

Bachelor of Science in Nursing
Active Delaware Nursing License
Active SOCRA or ACRP certification
American Heart Association BLS Certification

Key Skills

CSS
Cloud Computing
Health Education
Actuary
Building Electrician

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About Company

The Nemours Foundation

Nemours Children’s Health is an internationally recognized children’s health system. With more than 1.7 million patient encounters annually, we provide medical care in five states through two freestanding state-of-the-art children’s hospitals — Nemours Children’s Hospital, Delaware an ... View more

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