Senior Clinical Research Associate - Cra

Bighorn Law; Miami (FL); Hybrid; USD 85,000 - 115,000; Full time

Job summary

C-Clinical is seeking a Senior Clinical Research Associate to support clinical trials across the Miami region. The role blends remote responsibilities with routine on-site monitoring visits, enabling direct engagement with investigative teams.

The ideal candidate will bring hands-on CNS monitoring experience, strong site relationship management, and a commitment to regulatory and protocol compliance to ensure data quality, patient safety, and timely study execution across multiple sites.

Qualifications

• Experience in clinical monitoring with a focus on CNS studies (neurology/psychiatry).
• Strong ability to manage site relationships and maintain regulatory and protocol compliance.
• Proven track record ensuring data quality, patient safety, and study timelines.

Responsibilities

• Monitor investigations across multiple sites with routine on-site visits and remote support.
• Liaise with investigators, coordinators, and sponsors to ensure study progress and issue resolution.
• Oversee study conduct from startup through closeout, ensuring compliance with protocol and regulatory standards.

Skills

Clinical monitoring

Site management

Regulatory compliance

Study coordination

CNS studies experience

Job description

C-Clinical is seeking a Senior Clinical Research Associate to support clinical trials throughout the Miami region. This opportunity is ideal for an experienced clinical research professional who enjoys site interaction, study oversight, and helping ensure clinical trials operate efficiently from startup through closeout. The position combines remote responsibilities with routine on-site monitoring visits, allowing for both flexibility and direct engagement with investigative teams.

The ideal candidate has a strong background in clinical monitoring along with hands-on experience supporting central nervous system studies, including neurology and psychiatry indications. We are looking for someone who can confidently manage site relationships, review study activity with accuracy, and maintain a high standard of regulatory and protocol compliance throughout the trial process.

This position involves ongoing communication with investigators, coordinators, and sponsors while supporting data quality, patient safety, and study timelines across multiple research sites. Strong organizational skills, professionalism, and the ability to manage competing priorities are important within this environment.

C-Clinical values scientific excellence, collaboration, and operational consistency across every study we support. Our team is passionate about contributing to research that can positively impact patient care while creating an environment where experienced clinical professionals can continue to grow and contribute at a high level.