Aesthetic Clinical Research Assistant - On-Site Trials

BRIAN S. BIESMAN, MD, PLLC; Nashville (TN); On-site; USD 45,000 - 65,000; Full time

Job summary

Brian S. Biesman, M.D. PLLC in Nashville is seeking an experienced Clinical Research Assistant to join our on-site research team.

The role focuses on industry-sponsored trials in aesthetic medicine, requiring professional clinical research experience and strict adherence to GCP and protocol. The successful candidate will support participant visits, data capture, and regulatory documentation while collaborating with investigators, coordinators, sponsors, and monitors to ensure high-quality

Qualifications

• Minimum one year of paid, professional clinical research experience.
• GCP certification is required.
• Experience with industry-sponsored trials and clinical protocols.
• Strong attention to detail and ability to meet study deadlines.

Responsibilities

• Assist with day-to-day conduct of industry-sponsored clinical trials.
• Review study protocols and prepare for participant visits.
• Support recruitment, prescreening, scheduling, and retention.
• Assist with informed consent processes within training scope.
• Maintain regulatory documents and study files.
• Enter study data into EDC systems and resolve data queries.
• Coordinate site visits, monitoring, audits, and closeout activities.
• Communicate professionally with participants regarding appointments.

Skills

Attention to detail

Organizational skills

Communication skills

Time management

Regulatory knowledge

Education

GCP certification

Tools

EDC platforms

Job description

Brian S. Biesman, M.D. PLLC in Nashville is seeking an experienced Clinical Research Assistant to join our on-site research team.

The role focuses on industry-sponsored trials in aesthetic medicine, requiring professional clinical research experience and strict adherence to GCP and protocol. The successful candidate will support participant visits, data capture, and regulatory documentation while collaborating with investigators, coordinators, sponsors, and monitors to ensure high-quality