Clinical Research Assistant — Four‑Day Week

ADP, Inc.; Berry Hill (TN); On-site; USD 42,000 - 56,000; Full time

Benefits offered by this job

4-day work week

10-hour shifts Mon-Thu

Medical, dental, and vision insurance

401(k) with employer match

Paid time off and holidays

Paid holidays

Job summary

K2 Medical Research is seeking a Clinical Research Assistant to support our Nashville clinic. This role focuses on screening, coordinating with the Principal Investigator, and ensuring adherence to study protocols and regulatory standards.

You will collect patient information, maintain source documentation, and educate participants about clinical trials while collaborating with the Site Director and project teams in a fast-paced research environment.

Qualifications

• Outstanding verbal and written communication skills.
• Excellent interpersonal and customer services skills.
• Strong time management and organizational skills; in-depth knowledge of industry regulations.
• Proven ability to mentor others and foster organizational change.
• LPN, RN, or other medical licensure preferred.

Responsibilities

• Track and move candidates through screening efficiently.
• Coordinate with Principal Investigator and study team.
• Assist Site Director and Project Management on projects as needed.
• Adhere to the study protocol; obtain exemptions when necessary.
• Communicate protocol issues to CRO/Sponsor and site staff.
• Collect initial psychiatric and medical information from patients.
• Maintain source documentation and sponsor data.
• Dispense and maintain records of study medication.
• Educate patients and family about the study and trials.
• Complete all monitor and sponsor queries promptly.

Skills

Verbal communication

Written communication

Interpersonal skills

Time management

Organizational skills

Industry regulations knowledge

Mentoring

Education

HS Diploma or GED

Bachelor's degree preferred

Job description

K2 Medical Research is seeking a Clinical Research Assistant to support our Nashville clinic. This role focuses on screening, coordinating with the Principal Investigator, and ensuring adherence to study protocols and regulatory standards.

You will collect patient information, maintain source documentation, and educate participants about clinical trials while collaborating with the Site Director and project teams in a fast-paced research environment.