Clinical Research Coordinator II (Data) - Medical Oncology

Washington University in St. Louis; St. Louis (MO); In loco; USD 55.000 - 82.000; Tempo pieno

Descrizione del lavoro

Washington University in St. Louis is seeking a data coordinator to support multiple clinical research trials by extracting data from EMR and other sources and entering it into an Electronic Data Capture (EDC) system.

The role may involve coordinating data across many trials and ensuring accurate collection during protocol treatment and follow-up. The position requires collaboration with the clinic coordinator, PI, sponsors, vendors, and study teams to maintain compliance, patient safety, and

Competenze

• Bachelor's degree required.
• Clinical research experience 2 years required.
• SOCRA/ACRP certification preferred.

Mansioni

• 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 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.

Conoscenze

Clinical Research

Database Management

Spreadsheet Analysis

SAS

Data Review and Analysis

Formazione

Bachelor's degree

Strumenti

SAS

Descrizione del lavoro

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.

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 / 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.

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 employ