Registered Nurse Clinical Research Senior - Research Industry

CHRISTUS Health; San Antonio (TX); On-site; USD 65,000 - 80,000; Full time

Job summary

CHRISTUS Santa Rosa Health System seeks an experienced Research Coordinator RN to coordinate outpatient/inpatient research activities. You will liaise with investigators, manage regulatory documents, and monitor study data across CHRISTUS facilities.

The role requires prior nursing research experience, Texas RN licensure, and strong organizational skills. Work hours are 8 AM–5 PM, full-time, on site at Westover Hills.

Qualifications

• RN license required in Texas.
• BSN preferred; strong nursing background with research exposure.
• Experience in nursing research is required.
• Proficient with computer databases, spreadsheets and word processing.
• Excellent written and verbal communication skills.

Responsibilities

• Coordinate and collaborate with investigators to promote research within CHRISTUS Santa Rosa facilities.
• Prepare regulatory documents and assist with IRB submissions and renewals.
• Monitor regulatory compliance and data quality for studies.
• Create monthly summaries of studies for leadership review.
• Screen patients for protocol eligibility and assist with study medication management.

Skills

RN

Patient care

Communication skills

Organizational skills

Research protocols

Education

Bachelor's Degree in Nursing

Tools

MS Office

Databases

Spreadsheets

Job description

Summary

Coordinates, directs and implements research protocols. Provides advanced nursing skills in an outpatient research unit and/or inpatient unit involving research related efforts. This position is responsible for coordinating and collaborating with prospective investigators to promote, support and facilitate research at CHRISTUS Santa Rosa Health System. This position will promote CHRISTUS research services, educate investigators in the proper conduct of research, create and maintain research activity databases, and monitor the impact of research studies to include financial and safety risks. Will assist in project planning, and ensure that pre-established work scope, study protocol, and regulatory requirements are followed. Recruit and coordinate research subjects, as appropriate. Develop and maintain recordkeeping systems and procedures.

Responsibilities

• Facilitates the development of research studies with practitioners/ investigators interested in performing research at any of the facilities within the CHRISTUS Santa Rosa Health System. Functions as a liaison between clinical departments, support services, Medical Staff and administration to facilitate multi-disciplinary projects and teams for clinical research. Provides education, formal and informal, to departments, prospective investigators, Medical Staff and administration on the research process at CHRISTUS Health.
• Assists and educates researchers and their staff with the preparation of regulatory documentation and CHRISTUS Health applications for approval at both internal and external IRBs. Assists PIs in interaction with the IRB of record including submission, preparation of annual renewals, variances, closeout documentation, and preparation for regulatory audits.
• Evaluates proposed clinical research for operational impact on CSRHS, including adherence to the Ethical and Religious Directives for Catholic Healthcare, Catholic Social Teaching and the Mission, Vision and Values of Christus Health.
• Coordinates the information sharing of potential studies to all stakeholders that may be impacted in an effort to develop a reasonable plan of implementation.
• Creates monthly executive summaries of prospective and current studies for review by Leadership.
• Investigates and evaluates the financial impact of prospective studies, and any operational/financial issues that arise from existing studies.
• Monitors on-going clinical research for adherence to regulatory guidelines and determinations. Assists in the measurement and assessment of data from the Adverse Event Reports, including providing follow-up and feedback to staff, tracking and trending and preparing summary reports for Medical Staff and departments.
• Interacts with industry sponsors and PI research operations staff for industry-sponsored studies and management of sponsored research. Provides Clinical Research Coordinator role at CHRISTUS Santa Rosa hospitals.
• Collates and summarizes all market-wide research activities.
• Reviews invoices for research services provided by CHRISTUS departments that are remitted to funding body.
• Screens patients for protocol eligibility and participation in clinical trials.
• Participates in the coordination and monitoring of patient treatment and dispensing of study medication.
• Monitors and evaluates patient response to protocol treatment in collaboration with the physician.
• Provides education regarding study activities to patient, relatives and CHRISTUS Santa Rosa staff as necessary per protocol.
• Collect and/or process human specimens per protocol including blood, urine, sputum, buccal swabs, etc.
• Performs other professional nursing duties, including administration of medications, as required by protocol.
• Prepares regulatory documents for Institutional Review Board and/or sponsor.
• Develops and maintains Policies and Standard Operating Procedures for the Regional Clinical Research that outline the duties and responsibilities of the Regional Clinical Research Office and how those functions are carried out.
• Demonstrates competence to perform assigned responsibilities in a manner that meets the age-specific and developmental needs of members served by the Department.
• Appropriately adapts assigned assessment, treatment, and/or care methods to accommodate the unique physical, psychosocial, cultural, age-specific and other developmental needs of each member served.
• Takes personal responsibility to ensure compliance with all policies, procedures and standards as promulgated by state and federal agencies, the hospital, and other regulatory entities.
• Performs all duties in a manner that protects the confidentiality of patients and does not solicit or disclose any confidential information unless it is necessary in the performance of assigned job duties.
• Performs other duties as assigned.

Physical Location: CHRISTUS Santa Rosa - Westover Hills

Requirements

Education/Skills

• RN required
• Bachelor’s Degree in Nursing preferred.
• Proficient in using personal computer databases, spreadsheets and word processing software.
• Excellent oral and written communication skills.
• Excellent organizational skills and knowledge of federal legislation regarding human subject research and the provision of health care.
• Expertise in applying for and conducting research protocols.
• Must be able to produce clear and concise products.
• Must be flexible and be able to relate well with a variety of people.
• Must be knowledgeable in management applications and be able to expand and apply applicable skills in the work setting.
• Must have a strong customer service work ethic.
• Must have the ability to work independently.
• Must have the ability to meet deadlines.

Experience

• 2 years of experience in Nursing is required.
• Previous experience in research nursing is required.

Licenses, Registrations, or Certifications

• RN license in Texas is required.
• BLS certification is required; PALS is preferred.

Work Schedule:

8AM - 5PM Monday-Friday

Work Type:

Full Time