Clinical Trials Associate- Oncology

External 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 2,600 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.
What You Will Do
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.
Responsibilities
Tasks may include but are not limited to:

• Assist with the tracking and maintenance of project related information, including site medical question and answer log
• 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
• 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
• Arrange and track the distribution of project specific training to the project team
• Maintain current participating site and personnel information
• Generate and distribute minutes for a range of project related meetings, including Sponsor and Internal Management

Skills And Abilities

• Strong organizational and problem-solving skills
• Excellent written and verbal English as well as fluency of the language of the country of location
• Strong attention to detail and focus on quality of work
• Ability to work independently and as a team member
• Strong interpersonal skills
• Knowledge and understanding of ICH, GCP, and FDA or EU directive regulations (as applicable)
• Ability to handle multiple tasks and exercise independent judgment
• Sense of urgency and ability to be adaptable in a fast-paced and rapidly changing environment
• Excellent skills in MS Office applications including Outlook, Word, Excel and PowerPoint

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

Why Worldwide
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 clinical trial like a patient’s life depends on it – because it does. Our leaders are in the trenches with you - committed to advancing science and moving mountains for our customers. 
Interested in hearing more about Worldwide or our roles? Check out our careers page at www.worldwide.com/careers!
We’re a global, mid-size CRO that pushes boundaries, innovates and invents — because the path to a cure for the world’s most persist diseases is not paved by those who play it safe, but by those who take pioneering, creative approaches, and implement them with quality and excellence. We are experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs, in the best possible way.