Clinical Research Coordinator

Position Summary

As a Clinical Research Coordinator at Monroe Biomedical Research, you will play a critical role in the execution of clinical trials by managing patient interactions, performing study procedures, and ensuring the accuracy and integrity of collected data. This hands-on, dynamic position requires a detail-oriented professional who can work independently while collaborating with cross-functional teams to meet study goals. You’ll directly impact the success of groundbreaking clinical research studies, creating an exceptional patient experience and advancing the field of medicine.

Key Responsibilities

Study Management:

Design and maintain source documentation/workflows based on study protocol requirements.

Organize and schedule study patient visits.

Patient Interaction:

Perform study procedures and collect data from patients participating in clinical trials.

Procedures may include blood draws, ECGs, breathing tests, vital signs, etc.

Correspond with and mentor patients throughout the trial process.

Data and Records:

Review and process medical records.

Process and package laboratory specimens.

Submit and manage study data for pharmaceutical sponsors.

Required Qualifications

Associate’s degree or equivalent relevant experience required; bachelor’s degree preferred.

Healthcare background or professional experience as a nurse (LPN), clinical research coordinator, or medical assistant is preferred.

Experience working with patients is highly valued.

Ability to multitask and prioritize with poise and professionalism.

Demonstrated ability to be pleasant, tactful, and amicable while working with the public.

Strong desire to achieve a lead coordinator position within 12 to 18 months.