Clinical Trials Associate at Worldwide Clinical Trials

Seoul, , South Korea -

Full Time

Start Date

Immediate

Expiry Date

20 Aug, 26

Salary

0.0

Posted On

22 May, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Administrative Support, Project Tracking, Quality Auditing, Clinical Trial Documentation, Trial Master File Management, Meeting Minutes Generation, MS Office, ICH GCP, FDA Regulations, EU Directive Regulations, Interpersonal Skills, Problem-solving

Industry

Research Services

Description

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! The Clinical Trials Associate is 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. RESPONSIBILITIES: Tasks may include but are not limited to: Arrange and track system access for project team (Project Managers, Lead CRAs, CRAs, etc.) Maintain and quality audit to assure the most recent revisions of documents are on project portals Assist project team with preparation and shipment of clinical trial documentation, including Investigator Site File Maintain version and quality control of project documentation and submit to trial master file Assist with the tracking and maintenance of project related information, including site medical question and answer log Generate and distribute minutes for a range of project related meetings, including Sponsor and Internal Management Maintain current participating site and personnel information Arrange and track the distribution of project specific training to the project team Perform other duties as assigned The responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive. SKILLS AND ABILITIES: Excellent written and verbal English as well as fluency of the language of the country of location Strong interpersonal skills Ability to work independently and as a team member Sense of urgency and ability to be adaptable in a fast-paced and rapidly changing environment Ability to handle multiple tasks and exercise independent judgment Strong attention to detail and focus on quality of work Strong organizational and problem-solving skills Excellent skills in MS Office applications including Outlook, Word, Excel and PowerPoint Knowledge and understanding of ICH, GCP, and FDA or EU directive regulations (as applicable) REQUIREMENTS: 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. This is who we are. We’re a team of clinicians, scientists, and researchers who want to make healthcare better. We were founded on an unwavering commitment to authentic, personalized attention. And today, as CROs consolidate and the industry changes rapidly, that personalized attention is more important than ever. We all came to this industry for different reasons, from different walks of life. If you ask any one of us why we’re here, you’ll get a different answer. And that’s what makes us special. Not finding the right fit? Let us know you're interested in a future opportunity by clicking Get Started below or create an account by clicking 'Sign In' at the top of the page to set up email alerts as new job postings become available that meet your interest!

Responsibilities

The Clinical Trials Associate provides administrative and project tracking support to the clinical project team. Key duties include maintaining project portals, managing trial master files, and coordinating project-specific training.