Clinical Research Assistant — 4-Day Week (Nashville)

K2 Medical Research; Berry Hill (TN); On-site; USD 52,000 - 76,000; Full time

Benefits offered by this job

Medical, dental, and vision options

Supplemental insurance plans

401(k) with immediate employer match

Generous paid time off

Paid holidays

Four-day work week

Job summary

K2 Medical Research, a rapidly growing clinical research organization with a patient-first mission, seeks a Clinical Research Assistant to support our Nashville clinic. You will promote good clinical practices and ensure proper documentation under federal regulations and SOPs while coordinating with study teams.

Responsibilities include screening, coordinating with Principal Investigator, collecting initial patient information, maintaining source documentation, and educating patients about

Qualifications

• HS Diploma or GED required; Bachelor's degree strongly preferred.
• Experience in a clinical environment preferred; experience in clinical research ideal.
• LPN, RN, or other medical licensure or certification preferred.

Responsibilities

• Track and move candidates through screening efficiently.
• Understand studies through protocols and meetings; coordinate with Principal Investigator.
• Assist Site Director and Project Management on projects as needed.
• Adhere to study protocol; obtain exemptions when necessary.
• Communicate protocol issues to CRO and Sponsor; document via email/letter.

Skills

Verbal communication

Written communication

Time management

Organizational skills

Regulatory knowledge

Mentoring relationships

Education

HS Diploma or GED

Bachelor's degree preferred

LPN/RN licensure preferred

Job description

K2 Medical Research, a rapidly growing clinical research organization with a patient-first mission, seeks a Clinical Research Assistant to support our Nashville clinic. You will promote good clinical practices and ensure proper documentation under federal regulations and SOPs while coordinating with study teams.

Responsibilities include screening, coordinating with Principal Investigator, collecting initial patient information, maintaining source documentation, and educating patients about