Clinical Research Assistant (Contract)

Accelerated Clinical Trials; Snellville (GA); On-site; USD 21,000 - 34,000; Part time

Benefits offered by this job

Hands-on clinical research

Mentorship & development

Job summary

Accelerated Clinical Trials is seeking a Clinical Research Assistant (Contract) to support clinical trials under the direction of the Principal Investigator and clinical research team. This part-time role offers exposure to patient-facing activities and growth in healthcare or science.

The ideal candidate holds a health-related or science degree and demonstrates attention to detail, strong communication, and comfort working with study participants in clinical settings.

Qualifications

• Bachelor’s degree in a health-related or science field is preferred.
• Prior clinical research or patient care experience is preferred but not required.
• Strong attention to detail and organizational skills.
• Excellent communication and interpersonal abilities.
• Comfortable interacting with study participants in clinical settings.

Responsibilities

• Assist with participant recruitment, screening, and scheduling
• Support the informed consent process and maintain accurate study documentation
• Collect and record study data, vital signs, and study-specific assessments
• Prepare study materials and coordinate daily study operations
• Maintain regulatory and source documents (e.g., logs, binders, EDC entries)
• Communicate with participants, study staff, and external partners
• Follow Good Clinical Practice (GCP) and study protocols to ensure compliance

Skills

Attention to detail

Organizational skills

Communication

Interpersonal skills

Patient interaction

Education

Bachelor’s degree in health-related or science field

Job description

Job Title: Clinical Research Assistant (Contract)

Job Status: Part-time

Department: Clinical Research

Reports To: Clinical Research Manager

Job Summary

We’re seeking a motivated Clinical Research Assistant (Contract) to support clinical trials and research studies under the direction of the Principal Investigator and clinical research team. This role is ideal for candidates interested in clinical research, patient-facing work, and career growth in healthcare or science.

Key Responsibilities

• Assist with participant recruitment, screening, and scheduling
• Support the informed consent process and maintain accurate study documentation
• Collect and record study data, vital signs, and study-specific assessments
• Prepare study materials and coordinate daily study operations
• Maintain regulatory and source documents (e.g., logs, binders, EDC entries)
• Communicate with participants, study staff, and external partners
• Follow Good Clinical Practice (GCP) and study protocols to ensure compliance

Qualifications

• Bachelor’s degree in a health-related or science field (preferred)
• Prior clinical research or patient care experience (preferred, but not required)
• Strong attention to detail and organizational skills
• Excellent communication and interpersonal abilities
• Comfortable interacting with study participants in clinical settings

What We Offer

• Hands-on experience in clinical research and patient interaction
• Collaborative team environment with mentorship and professional development