Clinical Research Associate

Proclinical; Orlando (FL); Hybrid; USD 110,000 - 120,000; Part time

Job summary

Proclinical seeks a Clinical Research Associate to support a surgical imaging device study nearing closeout. The role involves a mix of onsite and remote monitoring, with most visits in Florida (Orlando and Tampa).

Potential pediatric sites in Philadelphia and Jacksonville may open next year. The focus is data cleaning and ensuring closeout readiness, with long-term growth as the sponsor plans in-house transitions.

Qualifications

• Proven experience in clinical monitoring, preferably within medical device studies.
• Strong understanding of GCP guidelines and regulatory requirements.
• Ability to work independently and manage multiple priorities effectively.
• Excellent communication and problem-solving skills.

Responsibilities

• Conduct onsite monitoring visits approximately 6-10 days per month, equating to 20-25 hours per week at sites.
• Oversee study progress, ensuring compliance with protocols, regulatory requirements, and data quality standards.
• Perform data cleaning and assist in preparing the study for closeout.
• Collaborate with site staff to address queries and resolve issues promptly.
• Support the opening of new study sites, including potential pediatric locations.
• Maintain accurate and timely documentation of monitoring activities.

Skills

Clinical monitoring

GCP knowledge

Independent worker

Communication

Travel willingness

Job description

Clinical Research Associate - Contract - Orlanda or Tampa, US

Are you ready to lead cutting-edge research projects that accelerate clinical breakthroughs in biotech?

Proclinical is seeking a Clinical Research Associate to support a surgical imaging device study nearing closeout.

Primary Responsibilities:

This role involves a mix of onsite and remote monitoring, with most site visits concentrated in Florida (Orlando and Tampa). Additional studies, including potential pediatric sites in Philadelphia and Jacksonville, are expected to open next year. The focus will be on data cleaning and ensuring the study wraps up successfully by year-end. This is an excellent opportunity for experienced CRAs looking for long-term growth, as the sponsor aims to transition CRAs in-house over time.

Skills & Requirements:

• Proven experience in clinical monitoring, preferably within medical device studies.
• Strong understanding of GCP guidelines and regulatory requirements.
• Ability to work independently and manage multiple priorities effectively.
• Excellent communication and problem-solving skills.
• Willingness to travel, primarily within Florida, with occasional trips to other locations.

The Clinical Research Associate's responsibilities will be:

• Conduct onsite monitoring visits approximately 6-10 days per month, equating to 20-25 hours per week at sites.
• Oversee study progress, ensuring compliance with protocols, regulatory requirements, and data quality standards.
• Perform data cleaning and assist in preparing the study for closeout.
• Collaborate with site staff to address queries and resolve issues promptly.
• Support the opening of new study sites, including potential pediatric locations.
• Maintain accurate and timely documentation of monitoring activities.

Compensation:

• $80 to $87 per hour.