Clinical Science Research Professional
Posted 2025-08-15
Remote, USA
Full Time
Immediate Start
About the position
The Clinical Science Research Professional will support the Fertility Preservation and Reproductive Late Effects (FPRLE) program within the Department of Obstetrics and Gynecology at the University of Colorado Anschutz Medical Campus. This full-time position involves assisting the research team in conducting clinical and community-based research focused on fertility and reproductive health. The role requires a strong understanding of biological and medical sciences, excellent communication skills, and the ability to work in a high-intensity research environment.
Responsibilities
• Assist with and oversee the day-to-day operations of clinical trials and studies.
,
• Obtain study subjects' medical history and current medication information, review research protocol inclusion/exclusion criteria, and confirm eligibility of subjects to participate in clinical trials.
,
• Perform informed consent process or ensure that the informed consent process has occurred, is properly documented, and that informed consent form documents are filed as required.
,
• Interview prospective subjects for a variety of research clinical trials and educate them on the details of the studies through phone contacts and personal interviews.
,
• Schedule subject participation in research clinical trials, coordinating availability of necessary space and clinical research support.
,
• Collect, code, and analyze data obtained from research in an accurate and timely manner.
,
• Adhere to research regulatory standards and maintain detailed records of studies to ensure compliance with FDA and other regulatory guidelines.
,
• Participate in subject recruitment efforts, including communicating with patients expressing interest and all pre-screening/screening activities.
,
• Ensure that the necessary supplies and equipment for studies are in stock and in working order.
,
• Independently master study materials, including protocols and informed consent forms for assigned studies.
,
• Independently perform study-related processes, procedures, and assessments as defined in study protocol and in compliance with regulating bodies.
,
• Assist Team Leads, Supervisors, and/or management with creation and implementation of processes and procedures and quality improvement initiatives.
,
• Act as a Primary Coordinator on multiple trials/studies and assist and train junior team members.
Requirements
• Bachelor's degree in any field.
,
• A combination of education and related technical/paraprofessional experience may be substituted for the bachelor's degree on a year-for-year basis.
,
• One (1) year clinical research or related experience.
Nice-to-haves
• One (1) year experience recruiting study participants for clinical trials.
,
• Bachelor's degree in science or health-related field.
,
• Two (2) years of clinical research or related experience.
,
• One (1) year experience with electronic data capture systems (e.g., EMR or EHR and data management systems).
,
• One (1) year of experience using REDCap.
,
• Experience with OB/GYN or sexual and reproductive health research.
,
• Experience as a project manager.
,
• Fluent in Spanish and able to pass an interpreter exam.
,
• Phlebotomy certification.
Benefits
• Health insurance
,
• Life insurance
,
• Retirement plan
,
• Tuition reimbursement
,
• Paid time off Apply tot his job
The Clinical Science Research Professional will support the Fertility Preservation and Reproductive Late Effects (FPRLE) program within the Department of Obstetrics and Gynecology at the University of Colorado Anschutz Medical Campus. This full-time position involves assisting the research team in conducting clinical and community-based research focused on fertility and reproductive health. The role requires a strong understanding of biological and medical sciences, excellent communication skills, and the ability to work in a high-intensity research environment.
Responsibilities
• Assist with and oversee the day-to-day operations of clinical trials and studies.
,
• Obtain study subjects' medical history and current medication information, review research protocol inclusion/exclusion criteria, and confirm eligibility of subjects to participate in clinical trials.
,
• Perform informed consent process or ensure that the informed consent process has occurred, is properly documented, and that informed consent form documents are filed as required.
,
• Interview prospective subjects for a variety of research clinical trials and educate them on the details of the studies through phone contacts and personal interviews.
,
• Schedule subject participation in research clinical trials, coordinating availability of necessary space and clinical research support.
,
• Collect, code, and analyze data obtained from research in an accurate and timely manner.
,
• Adhere to research regulatory standards and maintain detailed records of studies to ensure compliance with FDA and other regulatory guidelines.
,
• Participate in subject recruitment efforts, including communicating with patients expressing interest and all pre-screening/screening activities.
,
• Ensure that the necessary supplies and equipment for studies are in stock and in working order.
,
• Independently master study materials, including protocols and informed consent forms for assigned studies.
,
• Independently perform study-related processes, procedures, and assessments as defined in study protocol and in compliance with regulating bodies.
,
• Assist Team Leads, Supervisors, and/or management with creation and implementation of processes and procedures and quality improvement initiatives.
,
• Act as a Primary Coordinator on multiple trials/studies and assist and train junior team members.
Requirements
• Bachelor's degree in any field.
,
• A combination of education and related technical/paraprofessional experience may be substituted for the bachelor's degree on a year-for-year basis.
,
• One (1) year clinical research or related experience.
Nice-to-haves
• One (1) year experience recruiting study participants for clinical trials.
,
• Bachelor's degree in science or health-related field.
,
• Two (2) years of clinical research or related experience.
,
• One (1) year experience with electronic data capture systems (e.g., EMR or EHR and data management systems).
,
• One (1) year of experience using REDCap.
,
• Experience with OB/GYN or sexual and reproductive health research.
,
• Experience as a project manager.
,
• Fluent in Spanish and able to pass an interpreter exam.
,
• Phlebotomy certification.
Benefits
• Health insurance
,
• Life insurance
,
• Retirement plan
,
• Tuition reimbursement
,
• Paid time off Apply tot his job