A company is looking for a Clinical Trial Feasibility Specialist.
Key Responsibilities
Conducts comprehensive feasibility assessments and evaluates study protocols
Identifies and screens potential clinical research sites based on specific criteria
Prepares comprehensive feasibility reports and presents findings to internal stakeholders
Required Qualifications
Bachelor's degree in life sciences, health care, or a related field
At least 1 year of experience in site feasibility or study start-up at a clinical research multi-site organization
Strong understanding of clinical trial methodology and regulatory guidelines
Knowledge of medical terminology and ICH / GCP, regulatory requirements, FDA and HIPAA policies
Clinical Trial Specialist • Topeka, Kansas, United States