Clinical Research Coordinator II (Hybrid) - Radiology

Washington University in St. Louis; United States; Remote; USD 52,000 - 79,000; Full time

Job summary

A leading research institution is seeking a Clinical Research Coordinator to manage clinical trials within the Radiology Clinical Research Core. The role involves developing research plans, ensuring regulatory compliance, and overseeing participant recruitment. Ideal candidates will have a Bachelor’s degree and at least two years of clinical research experience. Join a dynamic team dedicated to advancing clinical theranostics research.

Qualifications

• At least 2 years of clinical research experience.

Responsibilities

• Coordinate research plans and manage all study phases.
• Evaluate clinical data and prepare reports.
• Assist in participant recruitment and oversee research staff.

Skills

Clinical Research

Study Protocols

Database Management

Statistical Software

Education

Bachelor’s Degree

Tools

SAS

Job description

Scheduled Hours

40

Position Summary

This position will be housed in the Radiology Clinical Research Core (RadCore) working directly with the Center for Clinical Theranostics Research (CCTR) coordinating clinical trials.

Mallinckrodt Institute of Radiology’s clinical theranostics program provides personalized medical management through targeted radiopharmaceutical diagnosis and therapy. Recognized as a Radiopharmaceutical Therapy Center of Excellence, it is a collaboration between the Division of Nuclear Medicine and the Department of Radiation Oncology.

Job Description

Primary Duties & Responsibilities:

1. Assist in developing research plans, interpreting results, and collaborating on manuscript and grant proposal preparation. Assist in protocol amendments and study design modifications as needed.
2. Coordinate the development of research forms, questionnaires, and techniques; assist in writing manuals; review scientific literature to stay updated on new developments.
3. Implement and manage all study phases, ensure compliance, establish record-keeping, assess participant progress, analyze adverse events, and liaise with funding agencies.
4. Evaluate and interpret clinical data; prepare reports and presentations; provide progress recommendations.
5. Ensure regulatory compliance, manage records, resolve protocol issues, and serve as a liaison with sponsors.
6. Assist in participant recruitment, develop recruitment plans, and oversee research staff involved in recruitment.
7. Enter data or supervise data entry staff using RedCap and online forms.
8. Coordinate specimen collection, handling, processing, and shipping.
9. Identify, screen, and enroll study subjects, ensuring proper sample and data collection.
10. Attend meetings, prepare study updates, and conduct clinical research visits.
11. Administer questionnaires, conduct functional and cognitive tests, complete medical histories, adverse event reports, and review outside records.
12. Work with study monitors on data queries and perform other assigned duties.

Working Conditions:

Job Location/Working Conditions: Normal office environment

Physical Effort: Typical sitting at a desk or table

Equipment: Office equipment

The above describes general work nature and is not exhaustive. Duties may be revised at management's discretion.

Required Qualifications

• Bachelor’s degree or equivalent experience.
• Basic Life Support certification from the American Heart Association or Red Cross.
• At least 2 years of clinical research experience.

Preferred Qualifications

• No additional education beyond required qualifications.
• Skills in clinical research, study protocols, database management, statistical software (SAS), and research projects.

Additional Details

Grade: C10

Salary Range: $52,600 - $78,900 annually, based on qualifications and performance.