Who we areWorldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications - from discovery to reality. Anchored in our company's scientific heritage, our dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases, is applied to develop flexible plans and solve problems quickly for our customers.Our talented team of 3,200+ professionals span 60+ countries. We are united in cause with our customers to improve the lives of patients through new and innovative therapies.Why WorldwideWe believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us!What Clinical Operations Site Management does at WorldwideClinical Trial Managers (CTMs) and Clinical Research Associates (CRAs) play a vital role in ensuring our clinical research programs are executed with the quality and excellence our sponsors expect and the care and passion patients deserve.These roles are the backbone of every strong CRO, helping drive breakthrough scientific research and playing a lead role on every clinical trial. All CROs will promise you growth, opportunity and maybe even a challenge. But we offer more than that.We offer an uncommon experience - one you can't get anywhere else, with a team unlike anyone else.At Worldwide we balance fun with the serious business of changing lives. We have a values-driven culture that is built from the ground up. We empower our team members to treat every trial like a patient's life depends on it - because it does. Our leaders are in the trenches with you daily - committed to advancing science and moving mountains for our customers.What you will doResponsible for managing the research activities at sites participating in Worldwide's clinical research projects, which are predominantly late phase (II-III).Conduct all types of visits - site qualifications, initiation, monitoring, site management and close out visits.Ensure adherence and compliance with Good Clinical Practices (GCPs)and applicable local and international regulations and Standard Operating Procedures (SOPs).Assure timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel.What you will bring to the roleExcellent interpersonal, oral, and written communication skills in EnglishSuperior organizational skills with attention to detailsAbility to work with little or no supervisionProficiency in Microsoft Office, CTMS and EDC SystemsYour experienceBachelor's Degree, (RN plus experience may be considered in lieu of a bachelor's degree).2+ years' regional CRA experience for as a Clinical Research Associate.Experience in oncology, rare diseases, respiratory disorders required.Ability to meet the travel requirements of the job. Our metrics are 6-8 days on site per month. Travel within the country.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 ! For more information on Worldwide, visit or connect with us on .
