Clinical Research Nurse

Innovo Research; Dubuque (IA); On-site; USD 70,000 - 95,000; Full time

Benefits offered by this job

Health Insurance

Dental Insurance

Disability Insurance

Life Insurance

Paid Time Off

Vision Insurance

Job summary

Innovo Research seeks a Clinical Research Nurse to join the team, providing direct patient care in clinical trials and ensuring regulatory adherence for patient safety and data integrity.

The role includes coordinating visits, screening, enrollment, and adverse event management, while maintaining licensing and training requirements. In-person, full-time work with comprehensive benefits is offered.

Qualifications

• Current RN/LPN licensure in the state of employment.
• Associate Degree in Nursing from an accredited school of nursing.
• Certification in Clinical Research Coordination (CCRC) preferred.
• BLS required
• Three years prior experience in a health-related clinic or research setting
• Proficient in the use of Microsoft Office applications
• Understanding of medical terminology
• Strong organizational skills
• Working knowledge of clinical trials
• Effective time management skills with the ability to multi-task and manage competing priorities with exceptional attention to detail.
• Ability to establish and maintain effective working relationships with physicians, coworkers, managers, and clients.
• Practice a high level of integrity, honesty, and in maintaining confidentiality.

Responsibilities

• Perform phlebotomy and monitor vital signs of study participants, educate family and contribute to care and evaluation of subjects.
• Manage multiple concurrent trials including screening, recruitment, enrollment, scheduling, coordinating procedures, visits and follow-up.
• Under supervision, conduct health assessments to assess or resolve adverse events and general health of study participants.
• Monitor study participants for adverse events and report to PI or study coordinator.
• Administer study interventions and treatments as directed by PI.
• Prepare administration, usage and documentation of investigational products.
• Maintain scope of nursing practice as per state boards.
• Maintain active nursing license status with state Board of Nursing.
• Perform diagnostic tests and monitor health through regular assessments.
• Observe and report changes in health status and provide clinical care when needed.
• Respond to emergencies and provide medical care per investigator direction.
• Maintain communication with research staff regarding enrollment and tasks.
• Assist in informed consent where appropriate.
• Support safety of research subjects.
• Collect, process and ship laboratory specimens.
• Comply with SOPs and regulatory guidelines.
• Provide training to new investigator/site staff and maintain training records.
• Performs all additional duties as assigned.

Skills

RN/LPN licensure

MS Office

Medical terminology

Strong organizational skills

Understanding of clinical trials

Time management

Ability to multi-task

Interpersonal skills

Education

Associate Degree in Nursing

Certification in Clinical Research Coordination (CCRC) preferred

Tools

Microsoft Office

Job description

A Clinical Research Nurse is a member of the research team who serves participants in clinical trials with direct patient care. This position is responsible for maintaining tight regulatory control over the health and safety of patients, as well as gathering and analyzing data for scientific study.

RESPONSIBILITIES

• Perform clinical functions i.e. phlebotomy, monitoring vital signs of study participants, etc., when warranted; educate family and contribute to the care and evaluation of subjects, including determining preliminary inclusion/ exclusion criteria.
• Manage multiple concurrent trials - screening, recruiting, and enrollment, perform patient/research participant scheduling, coordinate protocol-related research procedures, study visits, and follow—up, collect patient/ research participant history, collect, and maintain source documentation, perform data entry and query resolution, prepare IRB submissions, update required modifications, continuing reviews, and reportable events.
• Under the supervision of an investigator, conduct health assessments as medically necessary or required per protocol to assess or resolve adverse events, safety, and general health of study participants.
• Monitor study participants for adverse events and report any adverse events to the principal investigator, and study coordinator, if applicable.
• Administer study interventions and treatments as directed by the principal investigator, if appropriate for scope of license.
• Prepare and monitor administration, usage, and documentation of investigational products and other required treatments in clinical trials.
• Perform and adhere to clinical functions commensurate with pertinent nursing license scope of practice (i.e., keep within state Board of Nursing scope of practice for license as an LPN, RN, etc.)
• Maintain compliance with required hospital and unit-specific training competencies as well as an active nursing license status with the state Board of Nursing
• Perform diagnostic tests and monitor participants’ health through regular assessments.
• Observe, document, and report any changes in participant’s health status, and provide clinical care where necessary.
• Respond to emergencies and provide medical care as necessary and/or directed by a study investigator.
• Maintain frequent communication with research assistants and research coordinators regarding enrollment and tasks.
• Assist in the informed consent process of research subjects, if appropriate for scope of license.
• Support and advocate for the safety of research subjects.
• Collect, process, and ship laboratory specimens.
• Comply with Innovo, Clinic, and Sponsor policies, standard operating procedures (SOPs), applicable regulatory requirements and guidelines.
• Provide training to new investigator/site staff members on study-specific topics and requirements.Assist in maintaining adherence to investigator site staff training requirements by auditing and maintaining training records.
• Performs all additional duties as assigned.

A Clinical Research Nurse is a member of the research team who serves participants in clinical trials with direct patient care. This position is responsible for maintaining tight regulatory control over the health and safety of patients, as well as gathering and analyzing data for scientific study.

RESPONSIBILITIES

• Perform clinical functions i.e. phlebotomy, monitoring vital signs of study participants, etc., when warranted; educate family and contribute to the care and evaluation of subjects, including determining preliminary inclusion/ exclusion criteria.
• Manage multiple concurrent trials - screening, recruiting, and enrollment, perform patient/research participant scheduling, coordinate protocol-related research procedures, study visits, and follow—up, collect patient/ research participant history, collect, and maintain source documentation, perform data entry and query resolution, prepare IRB submissions, update required modifications, continuing reviews, and reportable events.
• Under the supervision of an investigator, conduct health assessments as medically necessary or required per protocol to assess or resolve adverse events, safety, and general health of study participants.
• Monitor study participants for adverse events and report any adverse events to the principal investigator, and study coordinator, if applicable.
• Administer study interventions and treatments as directed by the principal investigator, if appropriate for scope of license.
• Prepare and monitor administration, usage, and documentation of investigational products and other required treatments in clinical trials.
• Perform and adhere to clinical functions commensurate with pertinent nursing license scope of practice (i.e., keep within state Board of Nursing scope of practice for license as an LPN, RN, etc.)
• Maintain compliance with required hospital and unit-specific training competencies as well as an active nursing license status with the state Board of Nursing
• Perform diagnostic tests and monitor participants’ health through regular assessments.
• Observe, document, and report any changes in participant’s health status, and provide clinical care where necessary.
• Respond to emergencies and provide medical care as necessary and/or directed by a study investigator.
• Maintain frequent communication with research assistants and research coordinators regarding enrollment and tasks.
• Assist in the informed consent process of research subjects, if appropriate for scope of license.
• Support and advocate for the safety of research subjects.
• Collect, process, and ship laboratory specimens.
• Comply with Innovo, Clinic, and Sponsor policies, standard operating procedures (SOPs), applicable regulatory requirements and guidelines.
• Provide training to new investigator/site staff members on study-specific topics and requirements.Assist in maintaining adherence to investigator site staff training requirements by auditing and maintaining training records.
• Performs all additional duties as assigned.

Qualifications

Qualifications

• Current RN/LPN licensure in the state of employment.
• Associate Degree in Nursing from an accredited school of nursing.
• Certification in Clinical Research Coordination (CCRC) preferred.
• BLS required
• Three years prior experience in a health-related clinic or research setting
• Proficient in the use of Microsoft Office applications
• Understanding of medical terminology
• Strong organizational skills
• Working knowledge of clinical trials
• Effective time management skills with the ability to multi-task and manage competing priorities with exceptional attention to detail.
• Ability to establish and maintain effective working relationships with physicians, coworkers, managers, and clients.
• Practice a high level of integrity, honesty, and in maintaining confidentiality.

Benefits (full-time)

• Competitive Salary
• Health Insurance
• Dental Insurance
• Disability Insurance
• Life Insurance
• Paid Time Off
• Vision Insurance

WORKING CONDITIONS

This job operates in a professional and clinical environment with occasional visits to other Innovo Research partner sites/clinics. This role routinely uses standard office equipment such as computers, phones, and scanners. There is frequent exposure to communicable diseases, toxic substances, ionizing radiation, medicinal preparations, and other conditions common to a clinic environment. Varied activities include standing, walking, reaching, bending, and lifting.Requires full range of body motion including handling and lifting patients, manual and finger dexterity, and eye-hand coordination.Requires standing and walking for extensive periods of time.Occasionally lifts and carries items weighing up to 50 pounds.Requires corrected vision and hearing to normal range.

Due to the nature of this position, employees are expected to work in person.This is an exempt position under the federal and state wage and hour laws, which means you are not eligible for overtime pay beyond your salary.Employees are expected to work 40 hours a week. Occasional evening and weekend work may be required as job duties demand.

The above statements are intended to describe the general nature and level of work being performed by individuals assigned to this position. They are not intended to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel. More in-depth information can be found in SOP's, working guidelines, policies, etc. Innovo Research is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at Innovo are based on business needs, job requirements, and individual qualifications, without regard to race, color, religion or belief, national, social or ethnic origin, sex (including pregnancy), age, physical, mental or sensory disability, HIV Status, sexual orientation, gender identity and/or expression, marital, civil union or domestic partnership status, past or present military service, family medical history or genetic information, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. Innovo Research will not tolerate discrimination or harassment based on any of these characteristics. In addition, Innovo will provide reasonable accommodations for qualified individuals with disabilities.

Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.