Medical Assistant

Barrington James; Saint Petersburg (FL); On-site; USD 40,000 - 55,000; Full time

Job summary

A leading company is seeking a detail-oriented Research Assistant/Medical Assistant for a contract position in clinical research. The ideal candidate will have experience in clinical settings and strong organizational skills. Responsibilities include assisting with study coordination, ensuring regulatory compliance, and collaborating with clinical staff. This role is perfect for those looking to contribute to impactful research in a fast-paced environment.

Qualifications

• Minimum 1 year of experience in clinical research or a medical setting.
• Familiarity with GCP and ICH guidelines.

Responsibilities

• Assist with study coordination, including participant scheduling and data collection.
• Support regulatory compliance and proper documentation according to study protocols.

Skills

Attention to Detail

Communication

Organization

Education

Certified Medical Assistant

Tools

EDC Systems

Job description

Clinical Operations Recruitment Consultant - (Contract)

Job Title: Research Assistant / Medical Assistant (Clinical Research) – Contract

Location: Manhattan, NY

Contract Duration: 3–6 months

Schedule: 3 days a week, around 8 hours a day, 20-30 hours a week

Start Date: June

Overview:

We are seeking a detail-oriented and motivated Research Assistant/Medical Assistant with prior clinical research experience to support an ongoing study. This is a contract position (3–6 months) ideal for candidates with a strong understanding of clinical protocols and patient-facing responsibilities in a research setting.

Key Responsibilities:

• Assist with study coordination, including participant scheduling and data collection
• Support regulatory compliance and proper documentation according to study protocols
• Collect and record vital signs, medical histories, and study-related assessments
• Prepare and process laboratory specimens per protocol
• Ensure accurate and timely data entry into electronic data capture (EDC) systems
• Collaborate with clinical staff and investigators to maintain smooth study operations
• Assist with subject recruitment and informed consent process

Qualifications:

• Minimum 1 year of experience in clinical research or a medical setting
• Certified Medical Assistant (CMA) or equivalent clinical training preferred
• Familiarity with GCP (Good Clinical Practice) and ICH guidelines
• Strong attention to detail, organization, and communication skills
• Comfortable working in a fast-paced, research-driven environment
• Experience with EDC systems and basic phlebotomy (preferred but not required)

How to Apply:

Submit your CV to this job posting ASAP!