Research Nurse / Study Coordinator II
Inside Higher Ed, Gainesville, FL, United States
Study Coordinator II
Responsibilities include coordinating care and protocol‑required testing for subjects enrolled on an assigned portfolio of human clinical trials, interpreting and collecting medical and clinical data, maintaining compliance with regulatory requirements, and coordinating sample collection, analysis, and shipping.
Coordinate relevant care and protocol‑required testing for subjects enrolled on an assigned portfolio of human clinical trials.
Interpret and collect medical and clinical data for prospective and existing enrolled subjects on assigned clinical trials.
Maintain compliance with all internal and external regulatory and institutional requirements related to your trials.
Coordinate sample collection, analysis, and shipping for assigned trials.
Qualifications include a bachelor’s degree in health care, basic sciences, or related field; four to six years of relevant experience in clinical research, research coordination, or oncology preferred; extensive experience with research databases and subject‑level data management; proficiency in Microsoft Office Suite; strong time management, attention to detail, and ability to maintain confidentiality. A professional clinical research and/or oncology certification (SOCRA, ACRP, etc.) is required within 12 months of hire.
Bachelor’s degree in Health Care, Basic Sciences, or related field.
4–6 years of relevant experience in clinical research, research coordination, or oncology.
Extensive experience with research databases and subject‑level data management.
Proficiency in Microsoft Office Suite.
Excellent time management, attention to detail, and confidentiality.
Professional clinical research and/or oncology certification (SOCRA, ACRP, etc.) required within 12 months.
Preferred: Experience in oncology research and/or clinical trials coordination; forward‑thinking mindset; strong interpersonal and communication skills; ability to build relationships across multidisciplinary teams; strong customer service orientation.
Health Assessment Required: Yes.
Research Nurse
Responsibilities include subject care and navigation, facilitating appointments and data abstraction, coordinating treatment plans, communicating test results and counseling, aiding navigation of healthcare systems, serving as point of contact for subjects and their healthcare team, and coordinating care and protocol‑required testing. It also involves interpreting medical and clinical data, maintaining regulatory compliance, and coordinating sample collection, analysis, and shipping.
Subject care and navigation for enrolled subjects.
Facilitate appointments, consults, and data abstraction prior to visits.
Coordinate treatment plans with investigators, clinicians, and related staff.
Communicate test results, clarify and counsel as needed.
Aid subjects and families in navigating healthcare systems.
Serve as point of contact for subjects and healthcare team.
Coordinate relevant care and protocol‑required testing for subjects.
Interpret and collect medical and clinical data for subjects.
Maintain compliance with regulatory and institutional requirements.
Coordinate sample collection, analysis, and shipping.
Qualifications include a master’s degree in nursing or related field; six to eight years of relevant experience in clinical research or oncology; extensive experience with research databases and subject‑level data management; professional certification in clinical research (SOCRA or ACRP) and/or oncology (OCN); proficiency in Microsoft Office Suite; strong knowledge of clinical research processes and regulatory requirements; excellent organizational and documentation skills; and ability to manage complex workflows. A professional clinical research and/or oncology certification is required within 12 months of hire.
Master’s degree in Nursing or related field.
6–8 years of relevant experience in clinical research or oncology.
Extensive experience with research databases and subject‑level data management.
Professional certification in clinical research (SOCRA or ACRP) and/or oncology (OCN).
Proficiency in Microsoft Office Suite.
Strong knowledge of clinical research processes and regulatory requirements.
Experience with clinical research databases and data management systems.
Excellent organizational and documentation skills.
Strong ability to manage complex clinical and research workflows.
Professional clinical research and/or oncology certification required within 12 months.
Preferred: Experience in an academic or cancer center research environment; forward‑thinking; strong interpersonal and leadership skills; high emotional intelligence; strong customer service orientation.
Salary
Study Coordinator II: $60,000 - $67,500.
Research Nurse: $70,000 - $80,000.
Benefits
Teambs position with a suite of benefits, including retirement options and paid leave.
EEO Statement
The University of Florida is a member of the State University System of Florida and an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on merit.
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Responsibilities include coordinating care and protocol‑required testing for subjects enrolled on an assigned portfolio of human clinical trials, interpreting and collecting medical and clinical data, maintaining compliance with regulatory requirements, and coordinating sample collection, analysis, and shipping.
Coordinate relevant care and protocol‑required testing for subjects enrolled on an assigned portfolio of human clinical trials.
Interpret and collect medical and clinical data for prospective and existing enrolled subjects on assigned clinical trials.
Maintain compliance with all internal and external regulatory and institutional requirements related to your trials.
Coordinate sample collection, analysis, and shipping for assigned trials.
Qualifications include a bachelor’s degree in health care, basic sciences, or related field; four to six years of relevant experience in clinical research, research coordination, or oncology preferred; extensive experience with research databases and subject‑level data management; proficiency in Microsoft Office Suite; strong time management, attention to detail, and ability to maintain confidentiality. A professional clinical research and/or oncology certification (SOCRA, ACRP, etc.) is required within 12 months of hire.
Bachelor’s degree in Health Care, Basic Sciences, or related field.
4–6 years of relevant experience in clinical research, research coordination, or oncology.
Extensive experience with research databases and subject‑level data management.
Proficiency in Microsoft Office Suite.
Excellent time management, attention to detail, and confidentiality.
Professional clinical research and/or oncology certification (SOCRA, ACRP, etc.) required within 12 months.
Preferred: Experience in oncology research and/or clinical trials coordination; forward‑thinking mindset; strong interpersonal and communication skills; ability to build relationships across multidisciplinary teams; strong customer service orientation.
Health Assessment Required: Yes.
Research Nurse
Responsibilities include subject care and navigation, facilitating appointments and data abstraction, coordinating treatment plans, communicating test results and counseling, aiding navigation of healthcare systems, serving as point of contact for subjects and their healthcare team, and coordinating care and protocol‑required testing. It also involves interpreting medical and clinical data, maintaining regulatory compliance, and coordinating sample collection, analysis, and shipping.
Subject care and navigation for enrolled subjects.
Facilitate appointments, consults, and data abstraction prior to visits.
Coordinate treatment plans with investigators, clinicians, and related staff.
Communicate test results, clarify and counsel as needed.
Aid subjects and families in navigating healthcare systems.
Serve as point of contact for subjects and healthcare team.
Coordinate relevant care and protocol‑required testing for subjects.
Interpret and collect medical and clinical data for subjects.
Maintain compliance with regulatory and institutional requirements.
Coordinate sample collection, analysis, and shipping.
Qualifications include a master’s degree in nursing or related field; six to eight years of relevant experience in clinical research or oncology; extensive experience with research databases and subject‑level data management; professional certification in clinical research (SOCRA or ACRP) and/or oncology (OCN); proficiency in Microsoft Office Suite; strong knowledge of clinical research processes and regulatory requirements; excellent organizational and documentation skills; and ability to manage complex workflows. A professional clinical research and/or oncology certification is required within 12 months of hire.
Master’s degree in Nursing or related field.
6–8 years of relevant experience in clinical research or oncology.
Extensive experience with research databases and subject‑level data management.
Professional certification in clinical research (SOCRA or ACRP) and/or oncology (OCN).
Proficiency in Microsoft Office Suite.
Strong knowledge of clinical research processes and regulatory requirements.
Experience with clinical research databases and data management systems.
Excellent organizational and documentation skills.
Strong ability to manage complex clinical and research workflows.
Professional clinical research and/or oncology certification required within 12 months.
Preferred: Experience in an academic or cancer center research environment; forward‑thinking; strong interpersonal and leadership skills; high emotional intelligence; strong customer service orientation.
Salary
Study Coordinator II: $60,000 - $67,500.
Research Nurse: $70,000 - $80,000.
Benefits
Teambs position with a suite of benefits, including retirement options and paid leave.
EEO Statement
The University of Florida is a member of the State University System of Florida and an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on merit.
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