clinical research nurse

Nova Clinical Research, LLC

Nova Clinical Research is hiring a Clinical Research Nurse (RN) to support Phase I&ndash;IV clinical trials for medications and medical devices in a hospital setting. This role includes patient care, study coordination, and regulatory responsibilities starting at trial initiation.No prior research experience required&mdash;training provided.Responsibilities<ul><li>Provide direct patient care during study visits (vitals, ECGs, lab draws, monitoring)</li><li>Administer investigational medications and treatments per protocol</li><li>Screen, recruit, and enroll study participants</li><li>Coordinate and manage study visits and follow-ups</li><li>Monitor and report adverse events</li></ul>Regulatory / Start-Up:<ul><li>Assist with study start-up activities in the hospital</li><li>Prepare and maintain regulatory documents and binders</li><li>Support IRB submissions and approvals</li><li>Ensure compliance with study protocols, GCP, and regulatory requirements</li><li>Maintain accurate source documentation and data entry</li><li>Assist with monitoring visits and audits</li></ul>Requirements<ul><li>Active RN license (Florida)</li><li>1&ndash;3 years of hospital nursing experience in:</li><li>ICU</li><li>Med-Surg</li><li>Cath Lab</li><li>ER</li><li>Strong patient care and assessment skills</li></ul>Preferred<ul><li>Interest in clinical research</li><li>Experience with IVs, phlebotomy, or cardiac monitoring</li><li>BLS certification</li></ul>Benefits<ul><li>Health insurance</li><li>401(k)</li><li>Bonus opportunities</li></ul>Pay: $24.00 - $30.00 per hourBenefits:<ul><li>401(k)</li><li>401(k) matching</li><li>Dental insurance</li><li>Health insurance</li><li>Paid time off</li><li>Vision insurance</li></ul>Work Location: In person

Clinical Research Nurse

Innovo Research

<div>PLEASE NOTE: The location and site listed for this job are incorrect. This position will be located in Dubuque, Iowa.
JOB SUMMARY
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<ul><li>
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.</li><li>
Manage multiple concurrent trials - screening, recruiting, and enrollment, perform patient/research participant scheduling, coordinate protocol-related research procedures, study visits, and follow&mdash;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.</li><li>
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.</li><li>
Monitor study participants for adverse events and report any adverse events to the principal investigator, and study coordinator, if applicable.</li><li>
Administer study interventions and treatments as directed by the principal investigator, if appropriate for scope of license.</li><li>
Prepare and monitor administration, usage, and documentation of investigational products and other required treatments in clinical trials.</li><li>
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.)
</li><li>Maintain compliance with required hospital and unit-specific training competencies as well as an active nursing license status with the state Board of Nursing</li><li>
Perform diagnostic tests and monitor participants&rsquo; health through regular assessments.</li><li>
Observe, document, and report any changes in participant&rsquo;s health status, and provide clinical care where necessary.</li><li>
Respond to emergencies and provide medical care as necessary and/or directed by a study investigator.</li><li>
Maintain frequent communication with research assistants and research coordinators regarding enrollment and tasks.</li><li>
Assist in the informed consent process of research subjects, if appropriate for scope of license.</li><li>
Support and advocate for the safety of research subjects.</li><li>
Collect, process, and ship laboratory specimens.</li><li>
Comply with Innovo, Clinic, and Sponsor policies, standard operating procedures (SOPs), applicable regulatory requirements and guidelines.</li><li>
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.</li><li>
Performs all additional duties as assigned.</li></ul><div>
Qualifications<ul><li>
Current RN/LPN licensure in the state of employment.
</li><li>Associate Degree in Nursing from an accredited school of nursing.
</li><li>Certification in Clinical Research Coordination (CCRC) preferred.</li><li>
BLS required</li><li>
Three years prior experience in a health-related clinic or research setting</li><li>
Proficient in the use of Microsoft Office applications</li><li>
Understanding of medical terminology</li><li>
Strong organizational skills</li><li>
Working knowledge of clinical trials
</li><li>Effective time management skills with the ability to multi-task and manage competing priorities with exceptional attention to detail.</li><li>
Ability to establish and maintain effective working relationships with physicians, coworkers, managers, and clients.
</li><li>Practice a high level of integrity, honesty, and in maintaining confidentiality.</li></ul>
Benefits (full-time)</div><div><ul><li>
Competitive Salary</li><li>
Health Insurance</li><li>
Dental Insurance
</li><li>Disability Insurance</li><li>
Life Insurance</li><li>
Paid Time Off</li><li>
Vision Insurance</li></ul></div>
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.</div>

Spaulding Clinical

<div>THIS IS A FULL TIME NOC POSITION
Job Summary:
Responsible for basic nursing activities (such as, but not limited to, presenting Informed Consents, documenting medical history, Adverse Events (AE), Concomitant Medications (CM), performing drug administration/accountability, dose verification, focused subject physical assessments, collaborate with the medical team, IV placement, IV infusions, vital signs, ECG lead placement) in the conduct of clinical trials with emphasis on the safety and welfare of study participants. Performs the practical activities of clinical studies according to protocol, regulatory requirements, SOPs, scope of practice and current training status.
Essential Duties and Responsibilities:
<ul><li>With supervision, ensures that clinical trials are conducted according to protocol requirements by utilizing the following techniques &amp; procedures.</li><li>
Ensures subject has complete understanding of study-specific Informed Consent Form (ICF) and that all questions have been answered. Accurately documents and records completion of ICF.</li><li>
Obtains and accurately documents structured subject medical, surgical and medication history.</li><li>
Performs venipuncture, capillary, and/or IV specimens from study participants according to established protocol, maintains aseptic technique.</li><li>
Performs proper and accurate sample management, including collection, identification, transport, and/or processing of biological (blood, urine, etc.) study participants samples.</li><li>
Performs and records vital sign measurements (blood pressure, pulse oximetry, heartrate, temperature, respirations, etc.).</li><li>
Places ECG electrodes and leads accurately to ensure precise telemetry monitoring.</li><li>
Administers study drug and any other protocol-required medications, while accurately ensuring the 5 Rights of Medication Administration (the right subject, the right drug, the right dose, the right route, and the right time)</li><li>
Performs dose verification, assisting other staff members during dose administration to accurately verify subject identity and dosing labeling, as additional quality check.</li><li>
Contributes and is accountable for secure and appropriate storage of all drug supplies after removing from pharmacy.</li><li>
Records subject Adverse Events with proper escalation to medical or Charge Staff for evaluation and treatment as warranted.</li><li>
Performs additional task list items as delegated and supervised by Charge Staff or supervisor.</li><li>
Reviews Study Specific Trainings and applicable protocols for a thorough understanding of the study procedures, as they apply to their role and ensures that Delegation of Authority/Training Log for each study is completed in a proper and timely manner.</li><li>
Keeps abreast of SOPs, Good Clinical Practice (GCP) and ICH guidelines, state and national laws and ethical standards.</li><li>
Observes and maintains all HIPAA, OSHA, and Exposure Control regulations and Emergency Response as required by applicable training.</li><li>
Creates and maintains accurate records of all protocol activities and events, as delegated and trained.</li><li>
Follows the progress of study participants and provides for their care, comfort, and safety by attending to their needs during study participation.</li><li>
Participates in quality assurance of clinical research projects and initiates the need for same as it impacts on clinical practice.</li><li>
Trains staff in processes and procedures as needed.</li><li>
As required for study or site needs and if trained and delegated may be assigned study procedures such as obtaining participant information/histories/questionaries/meals/vital signs/EKGs/drug administration/specimen collection/luggage searches.</li><li>
Other functions as directed and delegated.</li></ul>
The Statements made in the job description are intended to describe the general nature and level of work being performed by people assigned to this job. These statements are not intended to be an exhaustive list of all responsibilities, duties and skills required of people assigned to this job.
Skills/Qualifications
<ul><li>Ability to read, write and interpret the English language.</li><li>
Portrays professionalism in all interactions at Spaulding Clinical.</li><li>
Good computer skills; inclination to adopt technology to maximize efficiency</li><li>
Demonstrates strong analytical, problem solving skills</li><li>
Strong written and verbal communication skills.</li><li>
Detail oriented, good organizational traits.</li><li>
Self-motivated</li><li>
Must be results-oriented, multi-tasking, quick learner, respond to the urgent needs of the team, and show a strong track record of meeting deadlines.
</li><li>Ability to work beyond normal work hours and various shift availability required.</li><li>
Ability to perform and record data entry via computer systems while conducting timed clinical procedures.</li></ul>
Physical Demands:
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
<ul><li>Ability to sit, stand, walk, reach with hands and arms, and use hands along with fingers, to handle or feel.
</li><li>Ability to lift and/or move up to 25 pounds.
</li><li>Specific vision abilities required by this job include clarity of vision both near and far.
</li><li>Ability to identify and distinguish colors.</li></ul>
Hazards:<ul><li>
Potential for exposure to toxic or caustic chemicals</li><li>
Potential for exposure to blood borne pathogens</li></ul>
Education and Experience:<ul><li>
Current RN or LPN License (Graduate Nurses must possess a temporary license in order to work as CRN, and must obtain Wisconsin licensure within 6 months of hire)
</li><li>BLS and ACLS certification required within 6 months of hire or promotion date</li></ul>
Spaulding Clinical Research management has the discretion to hire personnel with a combination of experience and education which may vary from the above listed skills and qualifications.</div>

Thomas Jefferson University & Jefferson Health

<div>Job Details
This Clinical Research Nursing position will be dedicated to the Neuromuscular Neurology Division within the Farber Institute for Neuroscience, working on Investigator Initiated and Industry Sponsored Trials. This position may require home visits with research participants.
Job Description
<ul><li>Performs basic nursing skills, study coordination, and data management
</li><li>Focuses on subject recruitment and enrollment
</li><li>Ensures consistency of study implementation
</li><li>Maintains data integrity and proper data management
</li><li>Ensures compliance with regulatory requirements and reporting
</li><li>Preferred experience in Neurology and Neuromuscular Disorders (e.g., Stiff Person Syndrome, Myasthenia Gravis)
</li><li>Interacts with co-workers, visitors, and staff in alignment with Jefferson values
</li><li>Collects and documents clinical data from study participants
</li><li>Provides patient education related to research studies
</li><li>Obtains informed consent and supports clinical trial enrollment
</li><li>Coordinates with consortium members and participating institutions
</li><li>Organizes and schedules meetings; records and distributes minutes
</li><li>Tracks and reports study progress
</li><li>May collect and process tissue specimens for analysis
</li><li>Collaborates with the research team on goals, implementation, and evaluation
</li><li>Supports adherence to protocol guidelines
</li><li>Assists in organizing and managing research data
</li></ul>Education:
Nursing Diploma or Associate&rsquo;s Degree in Nursing. BSN Preferred.
AND
Experience:
Minimum of 2 year of RN clinical experience in a health care setting. Clinical research experience preferred.
Minimum Certifications, Registration or License Requirements:
PA RN License
Work Shift
Workday Day (United States of America)
Worker Sub Type
Regular
Employee Entity
Thomas Jefferson University
Primary Location Address
901 Walnut Street, Philadelphia, Pennsylvania, United States of America
Nationally ranked, Jefferson, which is principally located in the greater Philadelphia region, Lehigh Valley and Northeastern Pennsylvania and southern New Jersey, is reimagining health care and higher education to create unparalleled value. Jefferson is more than 65,000 people strong, dedicated to providing the highest-quality, compassionate clinical care for patients; making our communities healthier and stronger; preparing tomorrow's professional leaders for 21st-century careers; and creating new knowledge through basic/programmatic, clinical and applied research. Thomas Jefferson University , home of Sidney Kimmel Medical College, Jefferson College of Nursing, and the Kanbar College of Design, Engineering and Commerce, dates back to 1824 and today comprises 10 colleges and three schools offering 200+ undergraduate and graduate programs to more than 8,300 students. Jefferson Health , nationally ranked as one of the top 15 not-for-profit health care systems in the country and the largest provider in the Philadelphia and Lehigh Valley areas, serves patients through millions of encounters each year at 32 hospitals campuses and more than 700 outpatient and urgent care locations throughout the region. Jefferson Health Plans is a not-for-profit managed health care organization providing a broad range of health coverage options in Pennsylvania and New Jersey for more than 35 years.
Jefferson is committed to providing equal educational and employment opportunities for all persons without regard to age, race, color, religion, creed, sexual orientation, gender, gender identity, marital status, pregnancy, national origin, ancestry, citizenship, military status, veteran status, handicap or disability or any other protected group or status.
Benefits
Jefferson offers a comprehensive package of benefits for full-time and part-time colleagues, including medical (including prescription), supplemental insurance, dental, vision, life and AD&amp;D insurance, short- and long-term disability, flexible spending accounts, retirement plans, tuition assistance, as well as voluntary benefits, which provide colleagues with access to group rates on insurance and discounts. Colleagues have access to tuition discounts at Thomas Jefferson University after one year of full time service or two years of part time service. All colleagues, including those who work less than part-time (including per diem colleagues, adjunct faculty, and Jeff Temps ), have access to medical (including prescription) insurance.
For more benefits information,</div>

Clinical Research Nurse - Neuromuscular Neurology

Parexel

<div>Shift: Per Diem/PRN - Day
Location: Baltimore, MD
Parexel Early Phase Clinical Unit supports the development of innovative new medicines which are vital for public health, improving outcomes, and saving lives. The early phase and &ldquo;first in human&rdquo; trials are the first step in testing these novel treatments in humans. 
At Parexel Baltimore Unit our highly trained and skilled nurses are the front-line staff involved in administering these new compounds to our volunteer participants via multiple routes, including, but not limited to, IV, IM, SC, PO, Topical, Inhalation etc. Then monitor the volunteer participants health status around the clock as per the trial protocol to ensure their safety and wellbeing.
Develop professionally by gaining experience in delivering high-quality research projects in this growing sector.
What you&rsquo;ll do after training is completed (including but not limited):<ul><li>
Support Standard Operating Procedures (SOPs), Good Clinical Practices (GCP), and all work processes to ensure the efficient and compliant clinical operation of the Early Phase Clinical Unit (EPCU).</li><li>
Assume responsibility for patient care and study conduct assignments.</li><li>
Ensure that all study laboratory and medical tests are completed, and that eligibility requirements specific to the assigned study are met. Assess compliance, symptoms, etc. per study protocol. Arrange for pre/post procedure laboratory work to be performed.</li><li>
Ensure that all established timelines relating to areas of responsibility and assigned projects are met.</li><li>
Participate and may direct identification and enrollment of study participants. Contributes to the development and implementation of study/research objectives.</li><li>
Assess, monitor, record, and report patient&rsquo;s condition and reaction to drugs and treatments to the appropriate physician.</li><li>
Collect and prepare data. Organize and enter data into case report forms.</li><li>
Enter data into databases when required. Assist physicians in completing flow sheets in medical records and progress notes. Update and maintain the contents of the Clinical Study File.</li><li>
Perform or arrange for phlebotomy, urine collection, sample preparation, storage and shipment of samples, drug dispensing, and follows GCP quality study documentation.</li><li>
Act as participant advocate in the conduct of clinical studies.</li></ul>
Qualifications<ul><li>
At least 2 years working in a hospital or clinical setting</li><li>
BSN preferred or relevant work experience.</li><li>
Active Registered Nurse License in the state of Maryland</li><li>
Current Basic Life Support (BLS) certification.</li><li>
ACLS certification required within 6 months of start date</li></ul>
Base Pay Range: $40.00 to $46.00 per hour
Actual salaries may vary within the range based on several factors including, but not limited to education, training, experience, professional achievement, and location.
In addition to base salary, some roles may be eligible for participation in Parexel&rsquo;s annual performance-based bonus plan, annual salary review and additional total rewards incentives. Our talent acquisition team will provide additional details on our bonus plan or incentive programs for those eligible roles. For all eligible employees, we offer market leading benefit programs including paid time off, 401k match, life insurance, health insurance, and other benefit offerings in accordance with the terms of applicable plans.
Parexel is dedicated to supporting, developing and retaining a diverse workforce, inclusive of veteran and military spouse talent. The skills and values you have developed are transferrable to meaningful careers here at Parexel. The following military career roles align with this position 66G, 66H, 68C, 4NOX1, 46NX, 66S, 66T, 290X.</div>

Clinical Research Nurse PRN/Per Diem

Inova Health System

<div>Inova Center for Personalized Health &amp; Inova Fairfax Hospital are looking for a dedicated Clinical Research Nurse Coordinator I to join the team Stem Cell &amp; Medicine Research Team. This role will be full-time, regular business hours: Monday &ndash; Friday, 8:00 a.m. &ndash; 5:00 p.m. (flexibility needed around specific research studies).
Inova is consistently ranked a national healthcare leader in safety, quality and patient experience. We are also proud to be consistently recognized as a top employer in both the D.C. metro area and the nation.
Featured Benefits:
<ul><li>Committed to Team Member Health: offering medical, dental and vision coverage, and a robust team member wellness program.
</li><li>Retirement: Inova matches the first 5% of eligible contributions &ndash; starting on your first day.
</li><li>Tuition and Student Loan Assistance: offering up to $5,250 per year in education assistance and up to $10,000 for student loans.
</li><li>Mental Health Support: offering all Inova team members, their spouses/partners, and their children 25 mental health coaching or therapy sessions, per person, per year, at no cost.
</li><li>Work/Life Balance: offering paid time off, paid parental leave, &amp; flexible work schedules. 
</li></ul>Clinical Research Nurse Coordinator I Job Responsibilities:
<ul><li>Provides patient education and medical information to study patients to ensure understanding of proper medication dosage, administration, and disease treatment.
</li><li>Delineates and defines the physiological status of the patient; assesses the educational, psychological and spiritual needs of the patient/significant other/family.
</li><li>Administers investigational medications and performs patient assessments during clinic visits to determine the presence of side effects; notifies treating investigator of findings/issues.
</li><li>Performs nursing duties as assigned and relevant to credentials and research study needs
</li><li>Identifies and explains key protocol elements; performs study tasks under direct supervision.
</li><li>Explains basic elements of subject safety including the reasoning behind the required use of an Institutional Review Board/Independent Ethics Committee, study activity documentation, and event reporting requirements. Demonstrates subject protection under direct supervision.
</li><li>Explains the investigational products development process and identify key regulations to control these processes.
</li><li>Explains and performs study operational activities in compliance with Good Clinical Practice (GCP) and non-GCP related study management activities.
</li><li>Explains how to document data according to ALCOA-C (Attributable, Legible, Contemporaneous, Original, Accurate and Complete) principles.
</li><li>Explains the importance of professional conduct and describe leadership principles that impact the effective operation of an investigative site.
</li><li>Explains the variety of communication channels, roles and relationship and outlets for study results that impact the conduct of clinical research.
</li>May perform other duties as assigned. 
<li>
</li></ul>Minimum Qualifications:
<ul><li>Education : BSN or AD. If RN has an AD, within six months from date of hire, they must meet with their nurse leader and conduct the following: 1.) Identify which accredited school they plan to attend 2.) Provide a written plan with anticipated BSN completion date 3.) Submit a review of transcripts from the school indicating the required pre-requisites and timeline for taking the courses 4.) Complete BSN within 24 months of start date.
</li><li>Experience : One (1) year of research training and/or protocol implementation.
</li><li>Certification : Basic Life Support from the American Heart Association; Must be eligible to practice as a Registered Nurse in VA 
</li></ul>Preferred Qualifications :
<ul><li>Experience : Strong clinical background in: ICU/oncology/medicine; research</li></ul></div>

Clinical Research Nurse Coordinator 1 - Stem Cell & Medicine

Vita Mobile Medical Support Services

<div>
 
 VitaMobile Medical Support Services
 
 has an urgent need for a
 
 per diem
 
 Registered Nurse to join our Clinical Research Team as a Mobile Clinical Research Phlebotomist.
 
 
 
 Study Visit Activities Include, But Are Not Limited To
 
 
 
 <ul>
 <li>
 Specimen collection, processing, packaging
 </li>
 <li>
 12-Lead ECG
 </li>
 <li>
 Collection of Vitals
 </li>
 <li>
 Study documentation
 
 
 </li>
 </ul>
 
 Requirements
 
 
 
 <ul>
 <li>
 Active and Unencumbered RN License
 </li>
 <li>
 Comfortable working with technology
 </li>
 <li>
 Recent home health experience (preferred)
 </li>
 <li>
 Reliable transportation
 </li>
 <li>
 Technologically savvy
 </li>
 <li>
 Available on weekdays during regular business hours
 </li>
 <li>
 Must have been involved in direct patient care within the last two years
 </li>
 </ul>
</div>

Mobile Clinical Research Nurse - Madison, AL

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Mobile Clinical Research Nurse - Madison, AL