Clinical Research Coordinator II (Data) - Medical Oncology

Washington University in St. Louis; St. Louis (MO); On-site; USD 55,000 - 82,000; Full time

Job summary

Washington University in St. Louis is seeking a Clinical Research Coordinator II (Data) in Medical Oncology to support investigators by extracting data from the EMR and source documents and entering it into the EDC system.

You may manage multiple trials, ensuring protocol data is collected accurately while patients are receiving treatment and during follow-up. The role requires a bachelor’s degree and at least two years of clinical research experience; SOCRA/ACRP certification is optional.

Qualifications

• Bachelor’s degree or combination of education and experience may substitute for minimum education.
• Clinical Research experience (2 years).
• SOCRA/ACRP certification is optional.
• Driver's license not required for this position.

Responsibilities

• Assists investigators as data coordinator for multiple clinical trials.
• Extracts data from EMR and source documents into EDC.
• Ensures accurate collection of protocol data during treatment and follow-up.
• Acts as liaison between school, trial sponsors, vendors, and study team.

Skills

Clinical Research

Clinical Study Protocols

Database Management

Research Projects

Spreadsheet Analysis

SAS

Education

Bachelor's degree

Job description

Clinical Research Coordinator II (Data) - Medical Oncology# Join us today## Clinical Research Coordinator II (Data) - Medical OncologyApply: On Campus/Onsite: Washington University Medical Campus: Full time: Posted Today: JR98273# **Location**St. Louis, MO 63110# **Scheduled Hours**40# **Position Summary**Assists investigators as a data coordinator of numerous 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, acts as liaison between the school, trial sponsors, vendors, and the study team. Responsible for helping the clinic coordinator and Principal Investigator (PI) manage and record data for all phases of study protocol as required by WU-IRB or sponsoring agency to ensure compliance, patient safety and welfare, and data integrity.# **Job Description****Primary Duties & Responsibilities:*** May perform duties inclusive of those delegated to a Clinical Research Coordinator I - Data.* May prepare oral or written presentations related to patient updates or protocol training.* May be involved in the design and creation of data report forms.* May be involved in the review and analysis of data.* Proactively identifies data issues and develops and implements process improvements.* May assist in the development of division wide corrective action plans in accordance with audit findings.* Serves as lead or as point of reference for other research coordinators for questions.* May be involved in interviewing, hiring, and providing oversight of staff.* Assists with onboarding and training of new data staff.* Provides feedback on performance and instruction to established staff.* Performs other duties incidental to the work described above.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****:**No specific certification/professional license is required for this position.**Work Experience:**Clinical Research (2 Years)**Skills:**Not Applicable**Driver's License:**A driver's license is not required for this position.# **More About This Job****Required Qualifications:*** (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, Database Management, Research Projects, Spreadsheet Analysis, Statistical Analysis Software (SAS)# **Grade**C10# **Salary Range**$54,600.00 - $81,900.00 / 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.