Systemart, LLC
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POSITION SUMMARY: The Clinical Research Nurse II (CRN II) will report directly to the Medical Director (MD) of the Cancer Clinical Trials Program and the Administrative Director in Hematology and Medical Oncology. The CRN II is primarily responsible for performing clinical and patient-facing tasks for patients on study. Will work with providers to identify potentially eligible patients for open clinical trials, and meet with potential research subjects to review consent forms and discuss trial requirements. Will see patients during required study visits and, partnering with the clinical research coordinator, ensure compliance with study requirements. The Clinical Research Nurse will also provide clinical perspective and information to regulatory coordinators as needed to facilitate trial activation.
As clinically facing research staff, it is expected that the Clinical Research Nurse will spend the majority of their time in clinic seeing active study patients and will be expected to follow and evaluate 4-6 patients per day 4 days/week (16-24 patients per week).
JOB RESPONSIBILITIES
Administrative:
Assists principal investigator with clinical trial protocol review process and protocol development as appropriate.
Collaborates with the quality assurance of clinical trials in developing protocol specific materials.
Research:
Assists with recruitment and registration of patients to clinical trials.
Coordinates scheduling of patient’s laboratory and radiographic assessments, admissions and clinic visits.
Monitors test results as appropriate.
Coordinates with clinical research coordinators and collaborates with staff within respective disease groups and with outside organizations in the completion of clinical research trials.
Clinical:
Coordinates study enrollment, protocol treatment, and completion of study requirements for patients participating in clinical trials.
Collaborates with Care Coordination for all patient care referrals. Collaborates with primary nurse (infusion, radiation, surgical) in assuring that patient care needs are met.
Provides protocol education to patients and families; adapts interactions based on age-specific, cultural and other needs of the patient.
Completes orders required specimens for analysis and monitors test results, as appropriate. Administers medications as necessary
Documents in charts as appropriate and communicates observations and findings to protocol investigator and attending physicians.
Provides protocol in-service training and serves as a resource to the health care team. Monitors the environment of care with attention to patient safety, and assures compliance with regulatory agency standards.
Maintains clinical practice that is evidence-based and consistent with nursing policies, procedures, licensure/registration requirements, and professional scope and standards.
JOB REQUIREMENTS
EDUCATION:
Graduate of an accredited nursing program
Baccalaureate Degree required
CERTIFICATES, LICENSES, REGISTRATIONS REQUIRED:
Licensed to practice professional nursing as a registered nurse (RN) in the Commonwealth of Massachusetts
Current basic cardiac life support certification
EXPERIENCE:
3-5 years research or clinical research experience is required
KNOWLEDGE AND SKILLS:
Ability at a basic level to input and analyze data and generate reports, especially in REDCap databases.
Ability to be highly organized, detail-oriented, and timely. Ability to analyze and solve problems in a systematic, logical, and timely manner.
Position requires tact and diplomacy to successfully motivate/educate subjects and staff, and knowledge of research regulations and research compliance requirements, including Protection of Human Subjects.
Must be able to maintain strict protocols of all confidential or sensitive information. Previous experience with grant writing, IRB submissions, data management, study coordination and database development, preferred.
Excellent English communication skills (oral and written). Bilingual or multi-lingual skills (beyond that of English) appropriate to the patient population served is a plus.
Cultural sensitivity and comfort with a wide range of social, racial and ethnic populations. Strong patient communication and patient education skills.
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Health Care Provider
Industries
Staffing and Recruiting
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Local Contract Registered Nurse Post Partum Registered Nurse, MDS Assessments (HYBRID-Temp) Nurse Educator - Outpatient Primary Care Lawrence, MA $90,000 - $100,000 15 hours ago
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Get AI-powered advice on this job and more exclusive features.
POSITION SUMMARY: The Clinical Research Nurse II (CRN II) will report directly to the Medical Director (MD) of the Cancer Clinical Trials Program and the Administrative Director in Hematology and Medical Oncology. The CRN II is primarily responsible for performing clinical and patient-facing tasks for patients on study. Will work with providers to identify potentially eligible patients for open clinical trials, and meet with potential research subjects to review consent forms and discuss trial requirements. Will see patients during required study visits and, partnering with the clinical research coordinator, ensure compliance with study requirements. The Clinical Research Nurse will also provide clinical perspective and information to regulatory coordinators as needed to facilitate trial activation.
As clinically facing research staff, it is expected that the Clinical Research Nurse will spend the majority of their time in clinic seeing active study patients and will be expected to follow and evaluate 4-6 patients per day 4 days/week (16-24 patients per week).
JOB RESPONSIBILITIES
Administrative:
Assists principal investigator with clinical trial protocol review process and protocol development as appropriate.
Collaborates with the quality assurance of clinical trials in developing protocol specific materials.
Research:
Assists with recruitment and registration of patients to clinical trials.
Coordinates scheduling of patient’s laboratory and radiographic assessments, admissions and clinic visits.
Monitors test results as appropriate.
Coordinates with clinical research coordinators and collaborates with staff within respective disease groups and with outside organizations in the completion of clinical research trials.
Clinical:
Coordinates study enrollment, protocol treatment, and completion of study requirements for patients participating in clinical trials.
Collaborates with Care Coordination for all patient care referrals. Collaborates with primary nurse (infusion, radiation, surgical) in assuring that patient care needs are met.
Provides protocol education to patients and families; adapts interactions based on age-specific, cultural and other needs of the patient.
Completes orders required specimens for analysis and monitors test results, as appropriate. Administers medications as necessary
Documents in charts as appropriate and communicates observations and findings to protocol investigator and attending physicians.
Provides protocol in-service training and serves as a resource to the health care team. Monitors the environment of care with attention to patient safety, and assures compliance with regulatory agency standards.
Maintains clinical practice that is evidence-based and consistent with nursing policies, procedures, licensure/registration requirements, and professional scope and standards.
JOB REQUIREMENTS
EDUCATION:
Graduate of an accredited nursing program
Baccalaureate Degree required
CERTIFICATES, LICENSES, REGISTRATIONS REQUIRED:
Licensed to practice professional nursing as a registered nurse (RN) in the Commonwealth of Massachusetts
Current basic cardiac life support certification
EXPERIENCE:
3-5 years research or clinical research experience is required
KNOWLEDGE AND SKILLS:
Ability at a basic level to input and analyze data and generate reports, especially in REDCap databases.
Ability to be highly organized, detail-oriented, and timely. Ability to analyze and solve problems in a systematic, logical, and timely manner.
Position requires tact and diplomacy to successfully motivate/educate subjects and staff, and knowledge of research regulations and research compliance requirements, including Protection of Human Subjects.
Must be able to maintain strict protocols of all confidential or sensitive information. Previous experience with grant writing, IRB submissions, data management, study coordination and database development, preferred.
Excellent English communication skills (oral and written). Bilingual or multi-lingual skills (beyond that of English) appropriate to the patient population served is a plus.
Cultural sensitivity and comfort with a wide range of social, racial and ethnic populations. Strong patient communication and patient education skills.
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Health Care Provider
Industries
Staffing and Recruiting
Referrals increase your chances of interviewing at Systemart, LLC by 2x
Get notified about new Clinical Research Nurse jobs in
Boston, MA .
Local Contract Registered Nurse Post Partum Registered Nurse, MDS Assessments (HYBRID-Temp) Nurse Educator - Outpatient Primary Care Lawrence, MA $90,000 - $100,000 15 hours ago
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr