Clinical Research Coordinator ; Data; Medical Oncology

Location

St. Louis, MO 63110

40

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.

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.

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.

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

C09

$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…