START Center for Cancer Research
Clinical Research Coordinator, RN
START Center for Cancer Research, Lake Success, New York, United States
Description
About The START Center for Cancer Research Join the world's largest early phase oncology clinical research network! The START Center for Cancer Research is revolutionizing cancer treatment through groundbreaking clinical trials that bring hope directly to patients. With an impressive global footprint spanning the United States, Spain, Portugal, and Ireland, we've completed over 1,300 studies that have led to 43 FDA/EMA approved therapies-including being the first to treat a patient with Keytruda, the most effective cancer drug in medical history. Unlike traditional Academic Medical Centers that reach only 20% of cancer patients, START brings cutting-edge trials directly to community hospitals where most patients receive care. By joining our team, you'll be part of an organization that's truly changing lives and shaping the future of cancer treatment worldwide. Learn more at STARTresearch.com.
We are hiring a
Clinical Research Coordinator, RN , for our
Lake Success
location. The Clinical Research Coordinator, RN supports early phase oncology trials under senior research staff guidance. This role ensures accurate, timely research conduct, adhering to protocols, regulatory standards, and patient safety. Responsibilities include direct patient interaction, data collection, maintaining Good Clinical Practice (GCP), overseeing multiple protocols, and coordinating patient participation. The CRC, RN implements and completes protocol requirements, ensuring accurate, up-to-date information is provided to the team.
Compensation Range:
The anticipated hourly rate for this position is
$39.42 - $44.23 per hour , depending on experience and qualifications, and based on a 40-hour workweek and annualized salary range of $82,000 to $92,000. This role is not commission-based. A full job description is available upon request.
Work Schedule:
Business hours are 8:00 AM to 4:30 PM, Monday through Friday, with some flexibility required to accommodate patient schedules and clinical trial needs. This position is based at our new Fort Worth center, where you'll have the exciting opportunity to help establish our laboratory operations from the ground up.
Location:
450 Lakeville Road, Lake Success, NY 11042
Essential Responsibilities: Communicate regularly with Study Sponsors, CROs, and staff regarding protocol status, questions, and concerns. Monitor day-to-day study conduct to ensure protocol, SOP, and Good Clinical Practice compliance. Review and create trial forms to ensure protocol compliance. Maintain organized study files with standardized labeling and filing procedures. Implement protocols and amendments, training staff on patient treatment and management. Assist with patient screening, eligibility determination, and informed consent process. Manage source documents, address protocol deviations, assist with case report forms, and submit Serious Adverse Event reports. Education & Experience:
Associate's degree in Nursing and RN license in state of New York. 2 years of clinical research experience, with a basic understanding of oncology Phase 1 trials. Strong attention to detail, accuracy in data collection, and ability to meet deadlines. Excellent organizational, time-management, and communication skills. Proficient in Microsoft Office Suite, clinical trial management software, and knowledge of GCP and regulatory requirements. Preferred Education and Experience:
Bachelor's degree in Nursing. Experience working in an oncology setting. Best-in-Class Benefits and Perks We value our employees' time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:
Comprehensive health coverage: Medical, dental, and vision insurance provided Robust retirement planning: 401(k) plan available with employer matching Financial security: Life and disability insurance for added protection Flexible financial options: Health savings and flexible spending accounts offered Well-being and work-life balance: Generous paid time off policy, holidays and weekends off Annual performance bonus: 10% annual bonus opportunity Educational assistance program: Support for your continued professional development Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.
Ready to be part of a team changing the future of cancer treatment? Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.
We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.
About The START Center for Cancer Research Join the world's largest early phase oncology clinical research network! The START Center for Cancer Research is revolutionizing cancer treatment through groundbreaking clinical trials that bring hope directly to patients. With an impressive global footprint spanning the United States, Spain, Portugal, and Ireland, we've completed over 1,300 studies that have led to 43 FDA/EMA approved therapies-including being the first to treat a patient with Keytruda, the most effective cancer drug in medical history. Unlike traditional Academic Medical Centers that reach only 20% of cancer patients, START brings cutting-edge trials directly to community hospitals where most patients receive care. By joining our team, you'll be part of an organization that's truly changing lives and shaping the future of cancer treatment worldwide. Learn more at STARTresearch.com.
We are hiring a
Clinical Research Coordinator, RN , for our
Lake Success
location. The Clinical Research Coordinator, RN supports early phase oncology trials under senior research staff guidance. This role ensures accurate, timely research conduct, adhering to protocols, regulatory standards, and patient safety. Responsibilities include direct patient interaction, data collection, maintaining Good Clinical Practice (GCP), overseeing multiple protocols, and coordinating patient participation. The CRC, RN implements and completes protocol requirements, ensuring accurate, up-to-date information is provided to the team.
Compensation Range:
The anticipated hourly rate for this position is
$39.42 - $44.23 per hour , depending on experience and qualifications, and based on a 40-hour workweek and annualized salary range of $82,000 to $92,000. This role is not commission-based. A full job description is available upon request.
Work Schedule:
Business hours are 8:00 AM to 4:30 PM, Monday through Friday, with some flexibility required to accommodate patient schedules and clinical trial needs. This position is based at our new Fort Worth center, where you'll have the exciting opportunity to help establish our laboratory operations from the ground up.
Location:
450 Lakeville Road, Lake Success, NY 11042
Essential Responsibilities: Communicate regularly with Study Sponsors, CROs, and staff regarding protocol status, questions, and concerns. Monitor day-to-day study conduct to ensure protocol, SOP, and Good Clinical Practice compliance. Review and create trial forms to ensure protocol compliance. Maintain organized study files with standardized labeling and filing procedures. Implement protocols and amendments, training staff on patient treatment and management. Assist with patient screening, eligibility determination, and informed consent process. Manage source documents, address protocol deviations, assist with case report forms, and submit Serious Adverse Event reports. Education & Experience:
Associate's degree in Nursing and RN license in state of New York. 2 years of clinical research experience, with a basic understanding of oncology Phase 1 trials. Strong attention to detail, accuracy in data collection, and ability to meet deadlines. Excellent organizational, time-management, and communication skills. Proficient in Microsoft Office Suite, clinical trial management software, and knowledge of GCP and regulatory requirements. Preferred Education and Experience:
Bachelor's degree in Nursing. Experience working in an oncology setting. Best-in-Class Benefits and Perks We value our employees' time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:
Comprehensive health coverage: Medical, dental, and vision insurance provided Robust retirement planning: 401(k) plan available with employer matching Financial security: Life and disability insurance for added protection Flexible financial options: Health savings and flexible spending accounts offered Well-being and work-life balance: Generous paid time off policy, holidays and weekends off Annual performance bonus: 10% annual bonus opportunity Educational assistance program: Support for your continued professional development Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.
Ready to be part of a team changing the future of cancer treatment? Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.
We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.