Worldwide Clinical Trials logo
Worldwide Clinical Trials

Established in 1986, Worldwide Clinical Trials is a privately held company and leading provider of clinical-trial research studies. As an employer, the company

Clinical Trials Associate

Location

Poland + 2 moreAll locations: Poland | Serbia | United Kingdom

Posted

90 days ago

Salary

0

Seniority

Mid Level

No structured requirement data.

Job Description

Clinical Trials Associate

Worldwide Clinical Trials

Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way. Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit. Why Worldwide We 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 a Clinical Trials Associate does at Worldwide As a Clinical Trials Associate, you are responsible for providing administrative and project tracking support to the clinical project team, ensuring tasks for all assigned projects with Project Delivery services are performed timely and accurately. What you will do - Arrange and track system access for project team (Project Managers, Lead CRAs, CRAs, etc.) - Maintain and quality audit to ensure the most recent revisions of documents are on the project portals - Assist the project team with the preparation and shipment of clinical trial documentation, including the Investigator Site File - Maintain version and quality control of project documentation and submit to the trial master file - Assist with the tracking and maintenance of project-related information, including site medical questions and answer logs What you will bring to the role - Excellent written and verbal English as well as fluency of the language of the country of location - Ability to handle multiple tasks and exercise independent judgment - Strong attention to detail and focus on the quality of work - Strong organizational and problem-solving skills - Excellent skills in MS Office applications, including Outlook, Word, Excel, and PowerPoint Your experience - Degree level qualification or equivalent experience plus a minimum of one years’ experience in a related role - Skill sets and proven performance equivalent to the above 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, ancestry, 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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Clinical Trial Associate

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Clinical Trial Associate ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Clinical Trial Associate (CTA) to join our diverse and dynamic team. As a CTA at ICON Plc, you will play a key role in supporting the management and execution of clinical trials by handling a range of administrative and operational tasks. You will contribute to the smooth execution of clinical trials through efficient coordination, documentation, and communication with various stakeholders. What You Will Be Doing: - Providing administrative support for clinical trials, including managing documentation, coordinating meetings, and maintaining trial-related records. - Assisting in the preparation and submission of regulatory documents and ensuring compliance with study protocols and regulatory requirements. - Collaborating with cross-functional teams to support trial operations and resolve any issues that arise during the course of the study. - Monitoring and tracking trial progress, including managing site communications and ensuring timely delivery of study materials. - Building and maintaining strong relationships with site staff and other stakeholders to facilitate smooth trial operations and support overall project success. Your Profile: - Advanced degree or certification in a relevant field such as life sciences, healthcare, or clinical research. - Extensive experience in a clinical trial support role, with a solid understanding of clinical trial processes and regulatory requirements. - Strong organizational and multitasking skills, with the ability to manage multiple tasks and projects effectively. - Proficiency in clinical trial management systems and relevant software, with a keen eye for detail in documentation and data management. - Excellent communication, interpersonal, and problem-solving skills, with the ability to work collaboratively with diverse teams and stakeholders. What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: - Various annual leave entitlements - A range of health insurance offerings to suit you and your family’s needs. - Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. - Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being. - Life assurance - Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here. Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply

Canada
Job Closed
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United States