Clinical Research Coordinator III - Pediatrics Hematology & Oncology

Washington University in St. Louis

Missouri

On-site

USD 58,000 - 90,000

Full time

14 days+

A complete application in a minute

Tailored resume and cover letter, ready to send.

Get past ATS filters

Benefits offered by this job

Vacation & holidays
Health insurance
Metro transit / U-Pass
Tuition assistance

Job summary

Washington University is seeking a Clinical Research Coordinator III for the Pediatrics Hematology & Oncology team. This role ensures study startup, regulatory document maintenance, and budget tracking while coordinating site visits and supporting PIs in planning new trials.

The position requires BLS certification within one month of hire and preference for CCRP/CRP credentials. The incumbent will interact with multiple departments to maintain IRB and federal compliance and will supervise staff

Qualifications

  • Bachelor's degree or combination of education and/or experience may substitute for minimum education.
  • Basic Life Support (BLS) certification required within one month of hire date.
  • SOCRA/ACRP certification may be preferred depending on department.

Responsibilities

  • Oversees protocol study start up, launch, submission, and maintenance of regulatory documents.
  • Assists in budget review and invoice tracking to ensure regulatory compliance.
  • Coordinates site visits by monitors and auditors and supports PI in developing plans for research projects.

Skills

Analyze Information
Clinical Research Management
Clinical Study Protocols
Database Management
Interpersonal Communication
Leadership
Oral Communications
Prioritization
Problem Solving
Research Projects
Spreadsheet Analysis
SAS
Supervision
Written Communication

Education

Bachelor's degree
Master's degree

Tools

SAS

Job description

## Clinical Research Coordinator III - Pediatrics Hematology & OncologyApplyremote type: On Campus/Onsitelocations: Washington University Medical Campustime type: Full timeposted on: Posted Todayjob requisition id: JR96455# **Location**SAINT LOUIS, MO 63110# **Scheduled Hours**40# **Position Summary**Position oversees and coordinates complex or multi-site clinical research studies; serves as a resource to provide comprehensive information to clinical research staff by promoting a smooth operation, preparation of regulatory compliance and interaction with other departments; responsible for assisting in budgetary reports and ensuring billing and regulatory compliance standards are maintained; may supervise clinical research staff# **Job Description****Primary Duties & Responsibilities:*** Manages protocol study start up and study launch, submission, and maintenance of essential regulatory documents; assists in budget review and invoice tracking; assists in scheduling and facilitating site visits by external and internal monitors and auditors; provides high level of direct and indirect support.* Works with PI to evaluate research procedures; confers with PI to assist in developing plans for research projects; provides input of feasibility, cost, and workload in regards to participating in new clinical trials.* Serves as a resource to clinical research staff, ensuring appropriate procedures, and explains policies and procedures; ensures that research projects are completed according to IRB and federal guidelines; Develops and implements policies and procedures; provides comprehensive direction to clinical research personnel; may participate in the hiring, training, and evaluation of clinical research staff.* Serves as a subject matter expert for clinical group and acts as a resource for protocol related questions; facilitates communication with PIs to ensure that study objectives are met in a timely manner; maintains a cooperative relationship with Hematology/Oncology and other divisions and departments; researches and recommends new methods and procedures to maintain standards and improve quality.* Provides study coordinator functions and performs all duties associated with the coordination and implementation of clinical research study/projects, data collection, and the management of data generated by study protocols; consents participants for non-therapeutic clinical trials .* Performs other duties incidental to the work described above.**Working Conditions:**Job Location/Working Conditions* Normal office environmentPhysical Effort* Typically sitting at a desk or a tableEquipment* Office equipmentThe above statements are intended to describe the general nature and level of work performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all job duties performed by the personnel so classified. Management reserves the right to revise or amend duties at any time.# **Required Qualifications****Education:**Bachelor’s degree or combination of education and/or experience may substitute for minimum education.**Certifications****/Professional Licenses****:**The list below may include all acceptable certifications, professional licenses and issuers. More than one credential, certification or professional license may be required depending on the role.Basic Life Support - American Heart Association, Basic Life Support - American Red Cross**Work Experience:**Clinical Research (3 Years)**Skills:**Not Applicable**Driver's License:**A driver's license is not required for this position.# **More About This Job****Required Qualifications*** BLS certification must be obtained within one month of hire date.* Basic Life Support certification (Online BLS certifications, those without a skills assessment component, are not sufficient to meet the BLS requirements).* Optional Based on Department) SOCRA/ACRP certification.# **Preferred Qualifications****Education:**Master's degree**Certifications****/Professional Licenses****:**Certified Clinical Research Professional (CCRP) - Society of Clinical Research Associates (SOCRA), Clinical Research Professional (CRP) - Association of Clinical Research Professionals (ACRP)**Work Experience:**Lead Position (1 Year)**Skills:**Analyze Information, Clinical Research Management, Clinical Study Protocols, Database Management, Interpersonal Communication, Leadership, Oral Communications, Prioritization, Problem Solving, Research Projects, Spreadsheet Analysis, Statistical Analysis Software (SAS), Supervision, Written Communication# **Grade**C11# **Salary Range**$58,300.00 - $90,400.00 / AnnuallyThe salary range reflects base salaries paid for positions in a given job grade across the University. Individual rates within the range will be determined by factors including one's qualifications and performance, equity with others in the department, market rates for positions within the same grade and department budget.# **Questions**For frequently asked questions about the application process, please refer to our External Applicant FAQ.# **Accommodation**If you are unable to use our online application system and would like an accommodation, please email CandidateQuestions@wustl.edu or call the dedicated accommodation inquiry number at 314-935-1149 and leave a voicemail with the nature of your request.All qualified individuals must be able to perform the essential functions of the position satisfactorily and, if requested, reasonable accommodations will be made to enable employees with disabilities to perform the essential functions of their job, absent undue hardship.# **Pre-Employment Screening**All external candidates receiving an offer for employment will be required to submit to pre-employment screening for this position. The screenings will include criminal background check and, as applicable for the position, other background checks, drug screen, an employment and education or licensure/certification verification, physical examination, certain vaccinations and/or governmental registry checks. All offers are contingent upon successful completion of required screening.# **Benefits Statement**Personal* Up to 22 days of vacation, 10 recognized holidays, and sick time.* Competitive health insurance packages with priority appointments and lower copays/coinsurance.* Take advantage of our free Metro transit U-Pass for eligible employees.* WashU provides eligible employees with a defined contribution (403(b)) Retirement Savings Plan, which combines employee contributions and university contributions starting at 7%.Wellness* Wellness challenges, annual health screenings, mental health resources, mindfulness programs and courses, employee assistance program (EAP), financial resources, access to dietitians, and more!Family* We offer 4 weeks of caregiver leave to bond with your new child. Family care resources are also available for your continued childcare needs. Need adult care? We’ve got you covered.* WashU covers the cost of tuition for you and your family, including dependent undergraduate-level college tuition up to 100% at WashU and 40% elsewhere after seven years with us.For policies, detailed benefits, and eligibility, please visit: https://hr.wustl.edu/benefits/
Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Clinical Research Coordinator I - Hematology
Clinical Research Coordinator I - Hematology

Washington University in St. Louis • Missouri

On-site
USD 49,000 - 74,000
Vacation & holidays
Metro U-Pass
Tuition assistance
+1
Clinical Research Coordinator I - Surgery Oncology
Clinical Research Coordinator I - Surgery Oncology

Washington University in St. Louis • Missouri

On-site
USD 49,000 - 74,000
Paid time off
Holiday pay
Health insurance
+5
Clinical Research Coordinator II - Surgery Oncology
Clinical Research Coordinator II - Surgery Oncology

Washington University in St. Louis • Missouri

On-site
USD 55,000 - 82,000
Vacation time
Holidays
Health insurance
+3
Clinical Research Coordinator I - Pediatrics Hematology & Oncology
Clinical Research Coordinator I - Pediatrics Hematology & Oncology

Washington University in St. Louis • Missouri

On-site
USD 49,000 - 74,000
Vacation up to 22 days
10 recognized holidays
Health insurance
+2
Clinical Research Coordinator I - Surgery
Clinical Research Coordinator I - Surgery

Washington University in St. Louis • St. Louis (MO)

On-site
USD 32,552 - 48,891
Up to 22 days of vacation
Free Metro transit U-Pass
Health insurance packages
Clinical Research Coordinator II - Surgery
Clinical Research Coordinator II - Surgery

Washington University in St. Louis • St. Louis (MO)

On-site
USD 36,162 - 54,222
Up to 22 days of vacation
Competitive health insurance
Free Metro transit U-Pass
+1
Clinical Research Coordinator II - Emergency Medicine
Clinical Research Coordinator II - Emergency Medicine

Washington University in St. Louis • St. Louis (MO)

On-site
USD 54,600 - 81,900
Vacation & holidays
Health insurance
Metro U-Pass transit benefit
+3
Clinical Research Coordinator I - Emergency Medicine
Clinical Research Coordinator I - Emergency Medicine

Washington University in St. Louis • St. Louis (MO)

On-site
USD 49,200 - 73,800
Vacation and sick time
Holiday pay
Health insurance
+2
Clinical Research Project Manager II - Cardiology
Clinical Research Project Manager II - Cardiology

Washington University in St. Louis • Missouri

On-site
USD 75,000 - 129,000
Health insurance
Metro transit U-Pass
Retirement plan (403b)
+1
Clinical Research Study Assistant II - Obstetrics and Gynecology
Clinical Research Study Assistant II - Obstetrics and Gynecology

Washington University in St. Louis • Missouri

On-site
USD 41,000 - 62,000
Vacation and holidays
Health insurance
Transit benefits
+1