NCBiotech
Senior Clinical Research Associate - CNS - Central U.S. - Remot
NCBiotech, Durham, North Carolina, United States, 27703
Overview
We are Worldwide Clinical Trials, a global midsize CRO with a mission to improve lives by working with passion and purpose every day. We are a global team of 3,500+ experts dedicated to changing the way the world experiences CROs by taking pioneering, creative approaches and executing with quality and excellence. We believe everyone plays an important role in making a world of difference for patients and their caregivers. We are committed to a diverse and inclusive environment that promotes collaboration and creativity. We are a workplace where people thrive by being themselves and are inspired to do their best work every day. What Clinical Operations does at Worldwide At Worldwide Clinical Trials, you will embark on a rewarding journey within Clinical Operations, where your contributions will impact the lives of patients. As a Clinical Research Associate (CRA) at Worldwide, you will work with brilliant minds across therapeutic areas including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. Collaboration with top-tier colleagues is encouraged and ingrained in our culture. Our commitment to advancing clinical research is supported within a team-oriented environment. In a CRA role, you will receive extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs. Regular touchpoints and coaching with your Line Manager ensure professional development remains a priority. We offer a clear career path and development toward Clinical Trial Manager roles. Our accessible Executive Leadership team is committed to advancing science and making a difference for patients worldwide. We offer an unparalleled experience where you can contribute to scientific breakthroughs and be at the core of every successful clinical trial. Join us at Worldwide! What you will do
Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects, predominantly registries and other non-interventional/observational studies. Involved in all stages of the clinical study, including identifying potential sites, conducting start-up activities, collecting regulatory documents, supporting contracts and budgets, training sites to collect data properly, and reporting safety events; managing site activities during maintenance and closing down study activities after completion. Conduct study initiation visits (SIVs). Ensure compliance with informed consent, reporting safety events, and adhering to regulatory requirements, with most site management performed remotely. What you will bring to the role Excellent interpersonal, oral, and written communication skills in English. Superior organizational skills with attention to detail. Ability to work with little or no supervision. Proficiency in Microsoft Office, CTMS and EDC Systems. Your experience 5+ years of experience as a Clinical Research Associate. 4-year university degree or RN/BSN in Nursing. Experience in CNS is required; Psychiatry/Rare Disease experience is a plus. Candidates must reside in the Central United States in close proximity to an international airport. Willingness to travel regionally required. We love knowing that someone is going to have a better life because of the work we do. To view our other roles, check out our careers page at Discover a world of difference at Worldwide. For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn. Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.
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We are Worldwide Clinical Trials, a global midsize CRO with a mission to improve lives by working with passion and purpose every day. We are a global team of 3,500+ experts dedicated to changing the way the world experiences CROs by taking pioneering, creative approaches and executing with quality and excellence. We believe everyone plays an important role in making a world of difference for patients and their caregivers. We are committed to a diverse and inclusive environment that promotes collaboration and creativity. We are a workplace where people thrive by being themselves and are inspired to do their best work every day. What Clinical Operations does at Worldwide At Worldwide Clinical Trials, you will embark on a rewarding journey within Clinical Operations, where your contributions will impact the lives of patients. As a Clinical Research Associate (CRA) at Worldwide, you will work with brilliant minds across therapeutic areas including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. Collaboration with top-tier colleagues is encouraged and ingrained in our culture. Our commitment to advancing clinical research is supported within a team-oriented environment. In a CRA role, you will receive extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs. Regular touchpoints and coaching with your Line Manager ensure professional development remains a priority. We offer a clear career path and development toward Clinical Trial Manager roles. Our accessible Executive Leadership team is committed to advancing science and making a difference for patients worldwide. We offer an unparalleled experience where you can contribute to scientific breakthroughs and be at the core of every successful clinical trial. Join us at Worldwide! What you will do
Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects, predominantly registries and other non-interventional/observational studies. Involved in all stages of the clinical study, including identifying potential sites, conducting start-up activities, collecting regulatory documents, supporting contracts and budgets, training sites to collect data properly, and reporting safety events; managing site activities during maintenance and closing down study activities after completion. Conduct study initiation visits (SIVs). Ensure compliance with informed consent, reporting safety events, and adhering to regulatory requirements, with most site management performed remotely. What you will bring to the role Excellent interpersonal, oral, and written communication skills in English. Superior organizational skills with attention to detail. Ability to work with little or no supervision. Proficiency in Microsoft Office, CTMS and EDC Systems. Your experience 5+ years of experience as a Clinical Research Associate. 4-year university degree or RN/BSN in Nursing. Experience in CNS is required; Psychiatry/Rare Disease experience is a plus. Candidates must reside in the Central United States in close proximity to an international airport. Willingness to travel regionally required. We love knowing that someone is going to have a better life because of the work we do. To view our other roles, check out our careers page at Discover a world of difference at Worldwide. For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn. Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.
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