Independent Clinical Research Officer

Job Summary

A company is looking for an Independent Clinical Research Officer to lead a holistic supplement observational study on a contract basis for 3-6 months.

Key Responsibilities

• Design and refine a mini observational study protocol aligned with IRB and FDA-compliant standards
• Collaborate to define measurable outcomes and assist in IRB submission for ethical oversight
• Recruit and screen study participants, oversee study implementation, and analyze study data

Required Qualifications

• Advanced degree in life sciences, public health, or clinical research (MPH or related field)
• 3-5+ years of clinical or observational research experience
• Experience in oncology-related research or integrative and holistic health studies
• Familiarity with IRB processes, GCP, and research ethics
• Strong project management and organizational skills