Clinical Research Coordinator

Clinical Research Coordinator

As a Clinical Research Coordinator at Monroe Biomedical Research, you will play a vital role in the successful execution of clinical trials. This hands-on position involves managing patient interactions, performing study-related procedures, and ensuring the accuracy and integrity of clinical data. We’re looking for a detail-oriented professional who thrives in a fast-paced environment, can work independently, and collaborates effectively with cross-functional teams to meet study objectives.

In this role, you will directly contribute to advancing innovative medical research while delivering an exceptional experience for study participants.

Key Responsibilities

Study Management

Develop and maintain source documentation and workflows in alignment with study protocols

Coordinate and schedule patient visits for clinical trials

Patient Care & Interaction

Conduct study procedures and collect clinical data from trial participants

Perform procedures such as blood draws, ECGs, pulmonary function tests, and vital signs

Guide, support, and communicate with patients throughout the duration of the study

Data & Documentation

Review and process medical records with accuracy and attention to detail

Prepare, handle, and ship laboratory specimens in compliance with protocols

Enter, manage, and submit study data to pharmaceutical sponsors

Required Qualifications

Associate’s degree or equivalent experience required; Bachelor’s degree preferred

Background in healthcare or experience as an LPN, Clinical Research Coordinator, or Medical Assistant preferred

Prior experience working directly with patients strongly preferred

Ability to manage multiple priorities while maintaining professionalism and accuracy

Strong interpersonal skills with a patient-centered approach

Demonstrated professionalism, tact, and strong communication skills

Growth Opportunity

Clear pathway to advance into a Lead Clinical Research Coordinator role within 12–18 months