Clinical Research Coordinator IV - Medical Oncology

Washington University in St. Louis; St. Louis (MO); On-site; USD 64,000 - 100,000; Full time

Job summary

Washington University in St. Louis is seeking a Clinical Research Coordinator IV for the Medical Oncology program in St. Louis, MO. The role oversees complex clinical trials, mentors staff, and coordinates multi-site studies under PI guidance.

The position requires a Bachelor’s degree (Master’s preferred), 4 years of clinical research, and leadership experience. Basic Life Support is required within one month of hire, with SOCRA/ACRP certification beneficial. Salaried, full-time at WashU.

Qualifications

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

Responsibilities

• Acts as primary liaison to the Principal Investigator to develop plans for investigator-initiated research projects; prepares budgets and assists in preparing grant proposals; writes or assists in writing initial study protocol and amendments to protocols or modifications to study design.
• Reviews journals, abstracts, and scientific literature to stay updated and inform planning of new studies.
• Prepares study progress reports and data safety monitoring reports for PI and funding agencies; interprets study data and prepares reports.
• May supervise and train research staff and provide performance feedback; assist with staff scheduling.

Skills

Analytical Thinking

Clinical Research

Interpersonal Communication

Leadership

Oral Communications

Prioritization

Problem Solving

Written Communication

Education

Bachelor's degree

Master's degree

Job description

Clinical Research Coordinator IV - Medical Oncology# Join us today## Clinical Research Coordinator IV - Medical OncologyApply: On Campus/Onsite: Washington University Medical Campus: Full time: Posted Today: JR98274# **Location**St. Louis, MO 63110# **Scheduled Hours**40# **Position Summary**Oversees and coordinates complex and multi-center clinical research studies and provides comprehensive experience and expertise in the overall planning, conduct and evaluation of clinical research. Performs mentorship and direction to the research program and team(s) incorporating mission focused principles of ethics, integrity, and collaboration and implementation. Coordinates with multidisciplinary teams to maintain continuity of care and human subject protection with a commitment to research integrity.# **Job Description****Primary Duties & Responsibilities:*** May perform duties inclusive of those delegated to a Clinical Research Coordinator III and/or Clinical Research Supervisor.* Works under the Principal Investigator’s (PI) guidance to meet the research objectives of the project(s). Provides oversight and coordinates complex and/or multi-site clinical research.* Utilizes critical thinking in the management of clinical trials.* May be assigned to special projects for the department’s/division’s research program (i.e., educational, policy development, written procedures, compliance strategies, development of standard operating procedures, auditing/monitoring of trials being conducted, etc.).* May assist in providing supervision to members of the research team including training of new staff; serving as point of reference for current research staff; staff scheduling and performance feedback.* Utilizes elements of project management to monitor ongoing financial state, patient recruitment milestones, and personnel resources necessary to conduct the research. May assist financial and grant administrators with federal and sponsor funded trials.* Researches and recommends new methods and procedures to maintain standards and improve quality.* May order supplies needed for the research projects and research group.* Investigator Initiated Research Project Specific Tasks + Acts as primary liaison to Principal Investigator (PI) to develop plans for investigator-initiated research projects; prepares budgets and assists in preparing grant proposals to sponsoring agencies; writes or assists in writing initial study protocol and instructional manuals; preparation of amendments to protocols and/or modification to study design, as appropriate. + Reviews journals, abstracts, and scientific literature to keep abreast of new developments and to obtain information regarding previous studies to aid in the planning of new studies. + Prepares study progress reports and data safety monitoring reports for PI and funding agencies. + May assist in the interpretation of study data and results; may prepare oral and written reports and presentations and/or assist with preparation of manuscripts for publication.* 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 (4 Years), Lead Position (1 Year)**Skills:**Not Applicable**Driver's License:**A driver's license is not required for this position.# **More About This Job****Required Qualifications:*** Basic Life Support certification + Online Basic Support certifications, those without a skills assessment component, are not sufficient to meet the Basic Life Support requirements. + Basic Life Support certification must be obtained within one month of hire date.* (Optional Based on Department) SOCRA/ACRP certification# **Preferred Qualifications****Education:**Master's degree**Certifications****/Professional Licenses****:**No additional certification/professional licenses unless stated elsewhere in the job posting.**Work Experience:**No additional work experience unless stated elsewhere in the job posting.**Skills:**Analytical Thinking, Clinical Research, Interpersonal Communication, Leadership, Oral Communications, Prioritization, Problem Solving, Written Communication# **Grade**C12# **Salary Range**$64,300.00 - $99,700.00 / 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 [e-mail] 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/# **EEO Statement**Washington University in St. Louis is committed to the principles and practices of equal employment opportunity. It is the University’s policy to provide equal opportunity and access to persons in all job titles without regard to race, ethnicity or shared ancestry, color, national origin, citizenship (where prohibited by federal law), age, religion, sex, sexual orientation, gender identity or expression, disability, protected veteran status, or genetic information. As a federal contractor, the university maintains affirmative action programs to implement its equal employment opportunity policy for individuals with disabilities and protected veterans, in accordance with Section 503 of the Rehabilitation Act of 1973, as amended, and the Vietnam Era Veterans’ Readjustment Assistance Act of 1974 (VEVRAA), as amended.