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The primary purpose of the Research Nurse Supervisor position is to provide supervision and coordination of research and protocol related clinical aspects of investigational trials in collaboration with the multidisciplinary team and external sponsors in order to achieve quality clinical trial outcomes. This position supervises research nurses and other research personnel as required for the designated department.

KEY FUNCTIONS

SUPERVISION OF RESEARCH PERSONNEL

Provides direct supervision over assigned clinical research nursing and coordinator personnel. Participates with new employee hiring process, including overseeing the ongoing development and orientation program for staff in alignment with applicable position descriptions.

Assigns workload as relates to protocol management; directs and assists research nurses and other research staff in all aspects of protocol management.

Maintains appropriate staffing levels and ensures fair distribution of workload among the clinical research staff. Reviews assignments on a routine basis in collaboration with the Supervisors of Clinical Studies.

Assures that direct reports adhere to all policies/procedures of the department and institution.

Evaluates performance of assigned staff through the departmental and institutional performance management system, and manages disciplinary actions as needed.

Provides professional and ancillary staff education concerning research protocols.

Coordinates educational activities for the research staff.

Conducts monthly clinical research staff meeting.

PROTOCOL MANAGEMENT

Consults with Principal Investigators (PI's) regarding ongoing clinical trial assignments. Works closely with Clinical Research Group (CRG) Leadership team and research nurse personnel to ensure consistency between protocol database and source documentation.

Assumes responsibility for the effective operation of research protocols in collaboration with the PI, Study Sponsor, and other members of the Clinical Research Group (CRG) management team.

Maintains knowledge of the research process and resources available for the efficient management of research projects.

Assess patients for protocol eligibility through personal interviews and/or medical record review in outpatient and inpatient settings.

Coordinates, evaluates, and follows the patient's participation in clinical trials.

Provides documentation in the patient's medical record or recruitment log per protocol and institutional requirements.

Identifies and develops methods of patient screening.

Assists the primary investigator and other members of the research staff in collection, analysis, and evaluation of data.

Retrieves protocol-related data as documented in the medical record and accurately enters it into a computerized database.

Evaluates response to treatment, treatment toxicities and adverse drug reactions and reports appropriately to the principal investigator, the Institutional Review Board (IRB) and the study sponsor.

Provides protocol summary reports as requested.

Utilizes computer statistical/data management systems, as necessary.

Participates in protocol-specific clinical tasks as needed.

Identifies and provides patient and family educational needs regarding treatment management, evaluation, and follow-up in clinical trials through talking with patients, person-to-person or by telephone and/or through written educational material.

If necessary, administers investigational medications, following acceptable nursing procedures/guidelines.

Assists in the coordination with the collection of appropriate research related tissues and blood samples.

Orders protocol-related tests and procedures. In collaboration with the Eckstein Laboratory staff, obtains pathology slides and blocks as needed.

Collaborates with the multidisciplinary team, as necessary.

ADMINISTRATIVE

Collaborates with the management team on research policies/processes and quality assurance initiatives.

Educates and trains the clinical research staff in the research charge capture process. Reviews research charge capture process to ensure protocol billing compliance per departmental and institutional policies.

Provides pertinent team information as requested by the GU Clinical Trials Team

In collaboration with the Clinical Research Group Supervisor team, ensures that all clinical research conducted by the department meets IRB, federal and/or guidelines and policies.

In collaboration with the Clinical Research Group Supervisor team, designs research tools to aid in data collection and analysis.

Represents the management team at departmental and institutional meetings.

Assists the GU Center Clinical Administrative Director (CAD) and Clinic Nurse Manager with integration and orientation of research staff members.

Interacts with GU Patient Access Center staff related to new patients, referrals, and protocol information; oversees the presentation of new clinical trials as indicated.

Assists in the preparation of departmental protocol audits.

Ensures accuracy in the reporting of effort for assigned research staff members.

PROJECT MANAGEMENT

Participates in departmental, intradepartmental, and institutional research related projects, committees, and initiatives.

Completes special projects and reports as requested by manager.

MAINTAINS A LEVEL OF PROFESSIONAL EXPERTISE THROUGH EDUCATIONAL ACTIVITIES

Attends appropriate departmental meetings and institutional continuing education programs.

Shares information and develops educational presentations for the standing Clinical Research Group Meeting and other CRG staff meetings.

Maintains working knowledge of current Code of Federal Regulation (CFR) and Good Clinical Practice (GCP) guidelines as well as a comprehensive understanding of the research trial process, including but not limited to eligibility and disease processes.

Attends approved off-site meetings, workshops, and conferences.

Provides professional and ancillary staff education concerning the institution, the department and research through monthly meetings.

Participates in national organizations that are oncology and research focused.

Demonstrates excellent oral and written communication skills when contacting other institutions, patients, and agencies. Assimilates pertinent information in order to compose written correspondence.

Other duties as required.

EDUCATION

Required:

Bachelor's degree in Nursing.

EXPERIENCE

Required:

Four years of registered nursing experience to include one year of research nursing and one year of lead/mentor, project management or supervisory experience.

Successful completion of the LEADing Self Accelerate and/or LEADing Self Discover programs may substitute for one year of required supervisory or management experience.

Completion of both programs can be substituted for a maximum of two years of supervisory or management experience.

LICENSURE / CERTIFICATION

Required:

All of the following:

Current State of Texas professional nursing license (RN).

Basic Life Support (BLS) or Cardiopulmonary Resuscitation (CPR) certification.

OTHER

Required:

Must pass pre-employment skills test as required and administered by Human Resources.

It is the policy of The University of Texas MD Anderson Cancer Center to provide equal employment opportunity without regard to race, color, religion, age, national origin, sex, gender, sexual orientation, gender identity/expression, disability, protected veteran status, genetic information, or any other basis protected by institutional policy or by federal, state or local laws unless such distinction is required by law. http://www.mdanderson.org/about-us/legal-and-policy/legal-statements/eeo-affirmative-action.html

Additional Information

• Requisition ID: 172570

• Employment Status: Full-Time

• Employee Status: Regular

• Work Week: Days

• Minimum Salary: US Dollar (USD) 98,500

• Midpoint Salary: US Dollar (USD) 123,000

• Maximum Salary : US Dollar (USD) 147,500

• FLSA: exempt and not eligible for overtime pay

• Fund Type: Soft

• Work Location: Hybrid Onsite/Remote

• Pivotal Position: Yes

• Referral Bonus Available?: Yes

• Relocation Assistance Available?: Yes

• Science Jobs: No

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