Clinical Research Coordinator IV- Winship Cancer Institute
Y-Axis, Atlanta, GA, United States
Clinical Research Coordinator IV - Winship Cancer Institute at Emory University
Atlanta, Georgia, United States - Full Time
Start Date: Immediate
Expiry Date: 30 Apr, 26
Experience: 5 year(s) or above
Remote Job: Yes
Telecommute: Yes
Skills: Clinical Trials Management, Research Administration, Budget Monitoring, Participant Recruitment, Compliance Auditing, Grant Proposal Development, Leadership, Staff Supervision, Study Protocol Implementation, Clinical Research Experience, Education, Problem Solving, Communication, Team Collaboration, Data Management, Patient Support
About the Role
Winship Cancer Institute, part of Emory University, seeks a qualified Clinical Research Coordinator IV to manage complex clinical research projects, supervise staff, ensure adherence to protocols, recruit participants, manage budgets, and perform compliance auditing.
Key Responsibilities
Recruit, orient, and supervise research administration staff or independently manage complex research administration activities for clinical trials.
Manage large or multiple smaller clinical research projects.
Oversee clinical trials information systems.
Supervise implementation and adherence to study protocols.
Monitor expenditures and adherence to study budgets and resolve CAS issues.
Educate research staff on policies, processes and procedures.
Develop and implement strategies for recruiting and retaining research participants in long‑term trials.
Audit operations, including laboratory procedures, to ensure compliance with regulations and identify corrective actions.
Plan, identify, and handle study‑related equipment and facilities needs.
Provide leadership in identifying and completing research grants, study materials, brochures and correspondence.
Develop and submit grant proposals.
Lead or chair committees or task forces to resolve significant issues.
Perform other related approved responsibilities as required.
Minimum Qualifications
High School Diploma or GED with nine years of clinical research experience.
Or two years of college in a scientific, health‑related, or business administration program with seven years clinical research experience.
Or Licensed Practical Nurse (LPN) with six years of clinical research experience.
Or bachelor's degree in a scientific, health‑related, or business administration program with five years of clinical research experience.
Or master's degree, MD or PhD in a scientific, health‑related, or business administration program with two years of clinical research experience.
Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC) preferred.
Equal Opportunity Statement
Emory University is an equal opportunity employer; qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, veteran status, or other protected characteristics. Emory University complies with all applicable laws and regulations regarding nondiscrimination, equal opportunity, and affirmative action.
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Atlanta, Georgia, United States - Full Time
Start Date: Immediate
Expiry Date: 30 Apr, 26
Experience: 5 year(s) or above
Remote Job: Yes
Telecommute: Yes
Skills: Clinical Trials Management, Research Administration, Budget Monitoring, Participant Recruitment, Compliance Auditing, Grant Proposal Development, Leadership, Staff Supervision, Study Protocol Implementation, Clinical Research Experience, Education, Problem Solving, Communication, Team Collaboration, Data Management, Patient Support
About the Role
Winship Cancer Institute, part of Emory University, seeks a qualified Clinical Research Coordinator IV to manage complex clinical research projects, supervise staff, ensure adherence to protocols, recruit participants, manage budgets, and perform compliance auditing.
Key Responsibilities
Recruit, orient, and supervise research administration staff or independently manage complex research administration activities for clinical trials.
Manage large or multiple smaller clinical research projects.
Oversee clinical trials information systems.
Supervise implementation and adherence to study protocols.
Monitor expenditures and adherence to study budgets and resolve CAS issues.
Educate research staff on policies, processes and procedures.
Develop and implement strategies for recruiting and retaining research participants in long‑term trials.
Audit operations, including laboratory procedures, to ensure compliance with regulations and identify corrective actions.
Plan, identify, and handle study‑related equipment and facilities needs.
Provide leadership in identifying and completing research grants, study materials, brochures and correspondence.
Develop and submit grant proposals.
Lead or chair committees or task forces to resolve significant issues.
Perform other related approved responsibilities as required.
Minimum Qualifications
High School Diploma or GED with nine years of clinical research experience.
Or two years of college in a scientific, health‑related, or business administration program with seven years clinical research experience.
Or Licensed Practical Nurse (LPN) with six years of clinical research experience.
Or bachelor's degree in a scientific, health‑related, or business administration program with five years of clinical research experience.
Or master's degree, MD or PhD in a scientific, health‑related, or business administration program with two years of clinical research experience.
Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC) preferred.
Equal Opportunity Statement
Emory University is an equal opportunity employer; qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, veteran status, or other protected characteristics. Emory University complies with all applicable laws and regulations regarding nondiscrimination, equal opportunity, and affirmative action.
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