Clinical Research Coordinator I (Data) - Medical Oncology

Washington University; St. Louis (MO); On-site; USD 49,000 - 74,000; Full time

Benefits offered by this job

Vacation & holidays

Health insurance

Transit benefit

Retirement plan (403(b))

Wellness programs

Job summary

Washington University in St. Louis seeks a Data Coordinator to support clinical research trials by extracting data from EMR and other sources and entering it into EDC systems.

You will work under the guidance of investigators to coordinate data collection and ensure protocol procedures are followed, managing multiple trials concurrently.

Qualifications

• Bachelors degree or equivalent combination of education and experience.
• Basic Life Support certification must be obtained within one month of hire.
• SOCRA/ACRP certification is optional depending on department.
• No specific work experience required for this position.

Responsibilities

• Assist PI-guided research to meet project objectives.
• Identify, screen, and enroll study subjects with the research team.
• Ensure protocol requirements are met and coordinate study procedures.
• Handle, process, and ship research specimens; manage source documentation.
• Submit reportable event reports to sponsor, IRB and regulators per protocol.

Skills

Clinical Research

Clinical Study Protocols

Communication

Computer Systems

Interpersonal Communication

Organizing

Research Support

Education

Bachelors degree

Job description

Location St. Louis, MO 63110 Scheduled Hours 40

Position Summary

Assists investigators as a data coordinator of clinical research trials of all complexities, extracting data from the Electronic Medical Record (EMR) and other source documents and entering it into an Electronic Data Capture (EDC). May be responsible for numerous research trials simultaneously. Helps ensure the accurate collection of study- required procedures while patients are receiving protocol treatment and are in active protocol follow-up.

Primary Duties & Responsibilities

• Works under the Principal Investigator’s (PI) guidance to meet the research objectives of the project.
• Assists with study start-up activities including IRB applications for initial review, modifications/amendments, continuing reviews, and reportable events.
• Works with research team to identify, screen, and enroll study subjects.
• Ensures protocol requirements are met, including but not limited to: direct contact with research participants; collection of basic health information; coordination of study related procedures; handling, processing, and shipping of research specimens; organization of source documentation and data entry.
• Prepares/submits reportable event reports to sponsor(s), IRB and regulatory agencies in accordance with the study protocol and established policies, procedures, and regulations.
• Collaborates with sponsor’s research associates during monitoring activities by providing study documentation, data clarifications, and reports, as necessary.
• Performs other duties incidental to the work described above.

Working Conditions

Job Location Normal office environment. Physical Effort Typically sitting at a desk or table. Typically standing or walking. Typically bending, crouching, stooping. Equipment Office equipment. The 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: No specific work experience is required for this position.

Skills: Not Applicable

Driver's License: A driver's license is not required for this position.

More About This Job

Required Qualifications: 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: No additional education unless stated elsewhere in the job posting.

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: Clinical Research, Clinical Study Protocols, Communication, Computer Systems, Interpersonal Communication, Organizing, Research Support

Salary Range

Grade C09 Salary Range $49,200.00 - $73,800.00 / Annually The 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.

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, 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.

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