Research Coordinator - Cardiology and Neurology
Advocate Aurora Research Institute LLC
Advocate Lutheran General Hospital - 1775 Dempster St
You'll coordinate sponsored clinical trials and biospecimen studies, covering both the clinical and administrative work.
Posted Oct 7
- Shift and hours
- Generally Monday to Friday, business hours Generally Monday-Friday, business hours40 hours a week
- Unit and setting
- Clinical Trials: Cardiovascular research provide professional nursing care to research patientsResearch study patients
- License
- RN license RN Preferred
- Term
- Per Diem
Do you qualify?
- Education
- Bachelor's in biology, health science, or nursing (or equivalent knowledge) Bachelor's Degree (or equivalent knowledge) in Nursing or related field.
- Experience
- Typically requires 2 years of experience in Research Typically requires 2 years of experience in Research.
- Also asks
- Knowledge of GCP, ICH, FDA guidance and HHS regulations
- Also asks
- Competency in EMR, Microsoft Office and computerized programs Competency in using Electronic Medical Record (EMR), Microsoft Office Suite, and other computerized programs
Preferred
- License
- RN preferred RN Preferred
What it pays
- Pay reviews
- Pay within the range, set by qualifications, skills, experience and training Base compensation listed within the listed pay range based on factors such as qualifications, skills, relevant experience, and/or training
Benefits
- BenefitsPaid Time Off programsPaid Time Off programs
- BenefitsMedical, dental, vision, life, and short- and long-term disabilityHealth and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability
- BenefitsFlexible Spending Accounts for health care and dependent careFlexible Spending Accounts for eligible health care and dependent care expenses
- BenefitsAdoption assistance and paid parental leaveFamily benefits such as adoption assistance and paid parental leave
- BenefitsRetirement plans with employer matchDefined contribution retirement plans with employer match and other financial wellness programs
- BenefitsEducational Assistance ProgramEducational Assistance Program
More benefits (6)
- Medical, dental, vision, life and Short- and Long-Term Disability
- Flexible Spending Accounts
- Defined contribution retirement plan with employer match
- Financial wellness programs
- Incentive pay for select positions
- Opportunity for annual increases based on performance
The role and schedule
- Day to day
- Liaison between sponsor and investigators Acts as a liaison between sponsor and investigators and as the primary protocol/project contact for team members and clinical staff.
- Day to day
- Recruiting, screening and enrolling research subjects recruitment, screening, and enrollment of research subjects
- Day to day
- Case report form completion and submission (EDC) development, completion and submission of case report forms (EDC)
- Day to day
- Study drug/device accountability study drug/device accountability
- Day to day
- Adverse event and serious adverse event reporting AE/SAE reporting
- Day to day
- Biospecimen procurement, processing and shipping Ensures that laboratory requirements are being met for specimen procurement, proper collection, processing and shipment of specimens.
- Day to day
- Review protocol amendments and research orders Reviews protocol amendments and updates, research related orders (in collaboration with Investigational Drug Services)
- Day to day
- Education on protocol information for research and clinical staff Plans, develops and implements educational plans to disseminate protocol/project information with research staff, investigators and clinical staff.
- Day to day
- Coach and mentor research team members Coaches and mentors research team members and other personnel.
- Charting
- EMR, Microsoft Office and computerized research programs
- Hours stated
- Generally Monday-Friday, business hours
- On call
- On-call rotation
- Travel
- May travel among sites, with road and weather exposure Position may require travel among sites and therefore there is exposure to road and weather conditions.
- Details
- Possible continuous exposure to blood, body fluids and radiation hazards, with protective clothing worn as needed
- Details
- Must function in a latex environment Ability to function in a latex environment.
- Details
- Sitting, standing, walking, lifting and reaching above shoulders through the shift Must be able to sit, stand, walk, lift, squat, bend, reach above shoulders and twist throughout shift.
- Details
- Normal office environment Exposed to a normal office environment.
The workplace
Your fit
Questions to ask
- Can you walk me through the pay period for the posted pay range and differentials?
- What should I expect for weekend, holiday, and rotation?
- What orientation, preceptor time, and ongoing unit support are included?
- How are patient load, floating, and staffing support handled day to day?
On your path
Cardiac is a specialty you move into. Start on tele or stepdown; cath lab and CVICU usually come later.
Original listing
Posted on Advocate Aurora Research Institute LLC’s careers page.
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Department
80048 Research - Clinical Trials: Cardiovascular
Status
Full time
Benefits Eligible
Yes
Hou rs Per Week
40
Schedule Details/Additional Information
RN Preferred Generally Monday-Friday, business hours
Pay Range
$30.70 - $46.05 Major
Responsibilities
Performs clinical and administrative coordination of sponsored clinical trials, research protocols/projects, and biospecimen collection studies, as applicable. Provides guidance to physicians, clinical staff and research team members. Coordinates assigned research studies in collaboration with other team members and key stakeholders, including but not limited to; study start-up, review of study CTA/budget/CTMS, IRB submissions, recruitment, screening, and enrollment of research subjects, development of mechanisms to maximize subject adherence to the research protocol, maintain source documentation, data collection (i.e. development, completion and submission of case report forms (EDC), study drug/device accountability, monitoring of subjects, AE/SAE reporting, study close out, and facilitates quality assurance inspections and audits.
Acts as a liaison between sponsor and investigators and as the primary protocol/project contact for team members and clinical staff. Plans, develops and implements educational plans to disseminate protocol/project information with research staff, investigators and clinical staff. Reviews protocol amendments and updates, research related orders (in collaboration with Investigational Drug Services), and study-specific workflows.
Ensures that laboratory requirements are being met for specimen procurement, proper collection, processing and shipment of specimens. Serves as Primary Research Coordinator on studies across multiple sites guiding research team members involved in the study and coordinates and tracks research activities across sites. Coaches and mentors research team members and other personnel.
Assist with implementation of educational training plans including orientation. Maintains competency in research computer applications Attends and participates in educational programs, meetings, and assigned committees. Licensed nurses will utilize advanced assessment skills to identify patient care problems, provide professional nursing care to research patients and support Research Coordinators in performing nursing activities as needed.
Licensure, Registration, and/or Certification Required: None Required. Education Required: Bachelor's Degree in Biology, or Bachelor's Degree in Health Science, or Bachelor's Degree (or equivalent knowledge) in Nursing or related field. Experience Required: Typically requires 2 years of experience in Research.
Knowledge, Skills & Abilities Required: Knowledge of Good Clinical Practices, International Conference of Harmonization, FDA Guidance documents, Department of Health and Human Services regulations, standard operating procedures. Ability to successfully conduct and manage a research study. Ability to mentor team members and to prepare training plans.
Excellent verbal and written communication skills, organizational and time management skills with ability to work under pressure and meet deadlines. Ability to problem solve and work independently with a high degree of accuracy and attention to detail. Must be able to establish a good rapport with patients, investigators and sponsors.
Competency in using Electronic Medical Record (EMR), Microsoft Office Suite, and other computerized programs Physical Requirements and Working Conditions: Must be able to sit, stand, walk, lift, squat, bend, reach above shoulders and twist throughout shift. Must have functional sight and hearing. Ability to function in a latex environment.
May be exposed to mechanical, electrical, chemical, and radiation hazards as well as blood and body fluids on a continuous basis; therefore, protective clothing (i.e., gown, mask, goggles, gloves, etc.) must be worn as necessary. Exposed to a normal office environment. Operates all equipment necessary to perform the job.
Position may require travel among sites and therefore there is exposure to road and weather conditions. This job description indicates the general nature and level of work expected of the incumbent. It is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities required of the incumbent.
Incumbent may be required to perform other related duties.
Our Commitment to You
Advocate Health offers a comprehensive suite of Total Rewards: benefits and well-being programs, competitive compensation, generous retirement offerings, programs that invest in your career development and so much more – so you can live fully at and away from work, including: Compensation Base compensation listed within the listed pay range based on factors such as qualifications, skills, relevant experience, and/or training Premium pay such as shift, on call, and more based on a teammate's job Incentive pay for select positions Opportunity for annual increases based on performance Benefits and more Paid Time Off programs Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability Flexible Spending Accounts for eligible health care and dependent care expenses Family benefits such as adoption assistance and paid parental leave Defined contribution retirement plans with employer match and other financial wellness programs Educational Assistance Program Note: Eligibility for programs listed above may depend on your FTE or status (e.g., full-time, part-time, per diem, temporary, etc.); please ask a Recruiter for more information during an interview.
About Advocate Health
Advocate Health is the third-largest nonprofit, integrated health system in the United States, created from the combination of Advocate Aurora Health and Atrium Health. Providing care under the names Advocate Health Care in Illinois; Atrium Health in the Carolinas, Georgia and Alabama; and Aurora Health Care in Wisconsin, Advocate Health is a national leader in clinical innovation, health outcomes, consumer experience and value-based care. Headquartered in Charlotte, North Carolina, Advocate Health services nearly 6 million patients and is engaged in hundreds of clinical trials and research studies, with Wake Forest University School of Medicine serving as the academic core of the enterprise.
It is nationally recognized for its expertise in cardiology, neurosciences, oncology, pediatrics and rehabilitation, as well as organ transplants, burn treatments and specialized musculoskeletal programs. Advocate Health employs 155,000 teammates across 69 hospitals and over 1,000 care locations, and offers one of the nation’s largest graduate medical education programs with over 2,000 residents and fellows across more than 200 programs. Committed to providing equitable care for all, Advocate Health provides more than $6 billion in annual community benefits.