Research Coordinator at Cardiovascular Associates of America

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Full Time

Start Date

Immediate

Expiry Date

06 Jun, 26

Salary

0.0

Posted On

08 Mar, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Trial Management, Patient Recruitment, Site Operations, Data Management, Regulatory Compliance, GCP, ICH Guidelines, Problem Solving, Time Management, Organizational Skills, Communication

Industry

Hospitals and Health Care

Description

Job Title: Clinical Research Coordinator Location: Orlando, Florida Job Type: Full-time This is an onsite position We are hiring a Clinical Research Coordinator for the Orlando Office. The Research Coordinator will be responsible to lead the growth and development of the research program while also working with other clinic staff on existing and new clinical trials. As part of CVAUSA’s national network, the Clinical Research Coordinator will have the opportunity to collaborate with teams across the country, making an impact on cardiovascular care both locally and nationwide. Position Overview: 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. Key Responsibilities: Clinical Trial Management: Oversee all aspects of clinical trials, including patient recruitment, screening, and enrollment. Ensure that protocols are followed meticulously. Site Operations: Handle day-to-day site management, ensuring that all activities comply with regulatory requirements and study protocols. Data Management: Collect, verify, and manage clinical trial data, ensuring it is accurate and complete. Communication & Reporting: Act as the primary point of contact for study sponsors, participants, and other stakeholders. Provide regular updates and progress reports. Regulatory Compliance: Ensure all documentation, including regulatory submissions and patient records, are kept up-to-date and in compliance with ethical and legal standards. Problem Solving & Innovation: Identify areas for process improvement and implement solutions to drive efficiency and enhance trial operations. What We’re Looking For: 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 rapid growth and bring fresh, 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. Experience & Qualifications: Clinical experience in cardiovascular medicine in any licensed role (i.e. RN, technologist, medical assistant, etc.) Bachelor’s degree in a relevant field (e.g., life sciences, healthcare, or clinical research) Experience managing clinical trials, leading the enrollment for multiple clinical trials, developing a research program Strong organizational and time management skills Clinical research certification (e.g., CCRP) is a plus Knowledge of GCP, ICH guidelines, and regulatory requirements

Responsibilities

The Research Coordinator will lead the growth and development of the research program while managing and overseeing all aspects of clinical trials and site operations, including patient recruitment and data management. Key duties involve ensuring meticulous protocol adherence, handling day-to-day site management, and maintaining regulatory compliance.