Senior Clinical Research Coordinator

Care Access; Saint Petersburg (FL); On-site; USD 60,000 - 90,000; Full time

Benefits offered by this job

PTO and holidays

Medical, dental, and vision insurance

HSA and FSA

Bi-weekly HSA employer contributions

Short-Term & Long-Term Disability

401(k) with company match

Relocation support

Job summary

Care Access is seeking a Clinical Research Coordinator to ensure GCP compliance while screening, enrolling, and monitoring study subjects. You will collaborate with investigators, sponsors, and site staff to maintain protocol adherence and data quality.

The role requires strong knowledge of federal regulations and GCP, experience with clinical trials databases and EDC/IVR systems, and excellent communication skills for diverse teams. This is an on-site, full-time position with travel as needed.

Qualifications

• Bachelor's degree or equivalent; preferred.
• 3 years of CRC experience required.
• Phlebotomy experience recently required.

Responsibilities

• Screen, enroll, and monitor subjects per GCP and protocol.
• Maintain protocol compliance and regulatory documentation.
• Interact with participants, investigators, and sponsors.
• Assist regulatory filings and source document creation/review.
• Plan recruitment and outreach efforts.
• Coordinate visits, visits scheduling, and site communications.
• Ensure training and study requirements are met.

Skills

GCP knowledge

Regulatory knowledge

Attention to detail

Organizational skills

Communication skills

Independent work

Problem solving

Medical/research terminology

Data entry accuracy

Education

Bachelor's Degree preferred

Tools

Clinical trials database

IVR systems

Electronic Data Capture (EDC)

MS Word

Excel

Job description

Care Access is seeking a Clinical Research Coordinator to ensure GCP compliance while screening, enrolling, and monitoring study subjects. You will collaborate with investigators, sponsors, and site staff to maintain protocol adherence and data quality.

The role requires strong knowledge of federal regulations and GCP, experience with clinical trials databases and EDC/IVR systems, and excellent communication skills for diverse teams. This is an on-site, full-time position with travel as needed.