Regulatory Associate: Four‑Day Week, Impactful Trials

K2 Medical Research; Tampa (FL); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Medical, dental, vision benefits

401(k) with employer match

Paid time off & holidays

Four-day work week (Mon-Thu, 10-hour)

Job summary

K2 Medical Research in Tampa, FL is seeking a Regulatory Associate to develop and maintain regulatory documents for clinical trials and to manage start-up, amendments, ongoing reporting, and close-out with IRB and sponsors.

You'll liaise with IRBs, sponsors, and clinical teams; ensure audit-ready regulatory files; and support tracking of regulatory submissions, logs, and training across the regulatory department.

Qualifications

• 2+ years of clinical research or regulatory experience.
• Bachelor's Degree required.
• CCRP preferred.

Responsibilities

• Prepare regulatory documents for new study submissions to IRB and sponsor.
• Maintain regulatory files in audit-ready status at all times.
• Report protocol deviations and serious adverse events to the IRB as required.
• Liaise with IRBs and sponsor; update trial teams on regulatory status.
• Assist in documenting and tracking regulatory submissions and approvals.

Skills

Interpersonal skills

Planning & organization

Communication skills

Attention to detail

Confidentiality

Initiative

Customer service

Critical thinking

MS Office & Outlook

Education

Bachelor's Degree

Job description

K2 Medical Research in Tampa, FL is seeking a Regulatory Associate to develop and maintain regulatory documents for clinical trials and to manage start-up, amendments, ongoing reporting, and close-out with IRB and sponsors.

You'll liaise with IRBs, sponsors, and clinical teams; ensure audit-ready regulatory files; and support tracking of regulatory submissions, logs, and training across the regulatory department.