Location:

Geisinger Cancer Center Knapper Clinic

Shift:

Days (United States of America)

Scheduled Weekly Hours:

40

Worker Type:

Regular

Exemption Status:

No

Job Summary:

We’re working to create a national model for improving health. Today, we’re focused on bringing our region services that improve every facet of life to drive total health, inside and out. Through professional growth, quality improvement, and interdisciplinary collaboration, we’ve built an innovative culture that allows nurses to grow their skillsets, develop their practice, and leverage their years of experience to build a rewarding, lasting career with impact.

Job Duties:

The LPN Clinical Research Coordinator is responsible for supporting clinical research as coordinator for multiple research studies and clinical trials within inpatient and outpatient care units. Serves in an expanded role to assess the appropriateness of patients for clinical research protocols. Under the direction of the physician, sees patients in the clinic and hospital to collect data required for the research protocols.

This role is full-time, 40 hours weekly; 8 am to 4:30 pm. Travel may be required to outreach clinics as needed for patient care and upon request.

A minimum of 3 years LPN experience is preferred, Prior Oncology and/or research experience is strongly preferred.

Certified Clinical Research Professional (CCRP) will be required in the future. This will be discussed further during the interview.

 

 

Benefits at Geisinger:
We offer a comprehensive benefits package starting on day one, including:

• Health, dental, and vision insurance
• Three medical plan choices, including expanded network options
• Pre-tax savings plans (FSA & HSA)
• Company-paid life, short-term, and long-term disability insurance
• 401(k) with automatic Geisinger contributions
• Generous PTO that accrues quickly
• Up to $5,000 in tuition reimbursement per calendar year
• MyHealth Rewards wellness program with financial incentives
• Family-friendly support: adoption/fertility assistance, parental leave, military leave, and Care.com membership
• Employee Assistance Program (EAP): mental health, legal guidance, childcare/eldercare referrals, and more
• Voluntary benefits: accident, critical illness, hospital indemnity, identity theft protection, pet insurance, and more

Job Duties:

• Participates in assessing feasibility of clinical research opportunities, including protocol and population assessments.
• Assists in preparation of submissions for Institutional Review Board consideration and provides oversight for all reporting obligations.
• Develops the research informed consent document in compliance with all applicable regulations.
• Responsible for conduct of the clinical trial, including but not limited to recruitment, screening, enrollment, follow-up, and retention of eligible subjects according to protocol requirements.
• Maintains responsibility for investigational drug and device accountability.
• Monitors study finances to comply with study-specific budget.
• Direct patient care in the context of the study protocol.
• Administers and monitors investigational drugs and devices as directed by the investigator and clinician within the scope of professional license or certification.
• Administers appropriate scales or other clinical measurements as needed within the scope of professional license or certification.
• Reviews medical records of patients, interviews patients and collaborates with investigators and clinicians to assess the appropriateness of patients for clinical trial enrollment.
• Collaborates with nursing staff and research personnel to incorporate all details of research protocol forms study related patient care within the scope of professional license or certification.
• Provides education to subjects and family on specific research protocols, potential risks, benefits, and reporting of health events.
• Serves as a liaison between the principal investigator and the study sponsor for adapting a multi-center protocol to the specific local environment.
• Serves as site representative during sponsor initiated study audits.
• Serves as a liaison between the principal investigator and outside regulatory agencies.

Position Details:

Work is typically performed in an office environment. Accountable for satisfying all job specific obligations and complying with all organization policies and procedures. The specific statements in this profile are not intended to be all-inclusive. They represent typical elements considered necessary to successfully perform the job.

Education:

Graduate from Specialty Training Program- (Required)

Experience:

Minimum of 3 years-Nursing (Preferred)

Certification(s) and License(s):

Licensed Practical Nurse - Default Issuing BodyDefault Issuing Body

Skills:

Communication, Multitasking, Organizing, Research Regulatory Environment, Teamwork

OUR PURPOSE & VALUES: Everything we do is about caring for our patients, our members, our students, our Geisinger family and our communities.

• KINDNESS: We strive to treat everyone as we would hope to be treated ourselves.
• EXCELLENCE: We treasure colleagues who humbly strive for excellence.
• LEARNING: We share our knowledge with the best and brightest to better prepare the caregivers for tomorrow.
• INNOVATION: We constantly seek new and better ways to care for our patients, our members, our community, and the nation.
• SAFETY: We provide a safe environment for our patients and members and the Geisinger family. 

We offer healthcare benefits for full time and part time positions from day one, including vision, dental and domestic partners. Perhaps just as important, we encourage an atmosphere of collaboration, cooperation and collegiality.

Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, pregnancy, genetic information, disability, status as a protected veteran, or any other protected category under applicable federal, state, and local laws.