Independent Clinical Research Officer
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
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
