Research Coordinator (In-person)

Cardiovascular Associates of America•Mesa, AZ

2d•Onsite

About The Position

As a Clinical Research Coordinator, you will play a key role in managing and overseeing all aspects of clinical trials and site operations. You will have the opportunity to take ownership of your projects, driving them forward with innovation, efficiency, and excellence. This is a fantastic opportunity for an ambitious, goal-oriented individual who thrives in an independent, fast-paced environment.

Requirements

Clinical experience in cardiovascular medicine in a licensed or clinical support role (e.g., RN, technologist, medical assistant)
Bachelor’s degree in a relevant field (e.g., life sciences, healthcare, or clinical research)
Experience managing clinical trials, leading enrollment across multiple studies, and supporting research program development
Strong organizational and time management skills
Knowledge of GCP, ICH guidelines, and regulatory requirements
Goal-Driven & Independent: You thrive in an autonomous work environment and take full ownership of your responsibilities.
Innovative & Results-Driven: You are eager to contribute to CVAUSA’s growth and bring effective solutions to the table.
Detail-Oriented & Highly Organized: You have the ability to manage multiple tasks and deadlines without sacrificing quality.
Strong Communicator: You can effectively communicate with stakeholders at all levels, including sponsors, site staff, and participants.

Nice To Haves

Clinical research certification (e.g., CCRP) is a plus

Responsibilities

Oversee all aspects of clinical trials, including patient recruitment, screening, and enrollment. Ensure that protocols are followed meticulously.
Handle day-to-day site management, ensuring that all activities comply with regulatory requirements and study protocols.
Collect, verify, and manage clinical trial data, ensuring it is accurate and complete.
Act as the primary point of contact for study sponsors, participants, and other stakeholders. Provide regular updates and progress reports.
Ensure all documentation, including regulatory submissions and patient records, are kept up-to-date and in compliance with ethical and legal standards.
Identify areas for process improvement and implement solutions to drive efficiency and enhance trial operations.