Clinical Research Technician / Assistant (underfill)
About the position
Responsibilities
• Actively recruit potential participants for clinical studies through outreach and database searches.
• Coordinate pre-screening, eligibility assessment, informed consent, and enrollment of study participants.
• Provide participants with information regarding study protocols, ensuring understanding of requirements, risks, and benefits.
• Maintain regular contact with study participants to monitor adherence and manage concerns.
• Conduct follow-up visits as specified in the study protocol, documenting participant health status and compliance issues.
• Accurately enter patient data into study databases, ensuring data integrity and completeness.
• Conduct quality control checks and resolve discrepancies in data entries.
• Prepare and submit IRB applications, renewals, and protocol deviation reports.
• Monitor regulatory timelines and ensure compliance with institutional and federal regulations.
• Schedule and coordinate study-related meetings and assist with the development of study protocols.
Requirements
• Associate degree in Health Science or equivalent experience.
• Minimum 1 year of directly related experience in clinical research and clinical trials or an advanced degree in a health-related area.
• Minimum 3 years of human subject experience in clinical, lab, or health regulations.
Nice-to-haves
• Understanding of medical terminology and experience in a large complex health care setting.
• Ability to effectively communicate with staff and faculty of all levels.
• Knowledge of university policies and procedures.
• Bachelor's degree in Health Science or equivalent experience.
Benefits
• Excellent medical, dental and vision coverage effective on the first day.
• 2:1 Match on retirement savings.
Apply Now
Apply Now
Responsibilities
• Actively recruit potential participants for clinical studies through outreach and database searches.
• Coordinate pre-screening, eligibility assessment, informed consent, and enrollment of study participants.
• Provide participants with information regarding study protocols, ensuring understanding of requirements, risks, and benefits.
• Maintain regular contact with study participants to monitor adherence and manage concerns.
• Conduct follow-up visits as specified in the study protocol, documenting participant health status and compliance issues.
• Accurately enter patient data into study databases, ensuring data integrity and completeness.
• Conduct quality control checks and resolve discrepancies in data entries.
• Prepare and submit IRB applications, renewals, and protocol deviation reports.
• Monitor regulatory timelines and ensure compliance with institutional and federal regulations.
• Schedule and coordinate study-related meetings and assist with the development of study protocols.
Requirements
• Associate degree in Health Science or equivalent experience.
• Minimum 1 year of directly related experience in clinical research and clinical trials or an advanced degree in a health-related area.
• Minimum 3 years of human subject experience in clinical, lab, or health regulations.
Nice-to-haves
• Understanding of medical terminology and experience in a large complex health care setting.
• Ability to effectively communicate with staff and faculty of all levels.
• Knowledge of university policies and procedures.
• Bachelor's degree in Health Science or equivalent experience.
Benefits
• Excellent medical, dental and vision coverage effective on the first day.
• 2:1 Match on retirement savings.
Apply Now
Apply Now