Scientific Associate, Document Coordinator **New Biology Grads Welcome**

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 almost 2,500 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.

What the Scientific Associate, Document Coordinator does

The Scientific Associate, Document Coordinator with direct supervision is responsible for the QC reviewing or generation of final reports and Analytical Test Methods (ATMs) for studies conducted at Worldwide Clinical Trials. The individual should have experience and working knowledge in reviewing scientific and regulatory reports and the ability to meet regulatory and Sponsor requirements. This individual performs routine work with general oversight and meets timelines.

What you will do

• Review or compile study reports for accuracy and compliance with Worldwide’ s SOPs, client guidelines and current regulatory guidance
• Review and update controlled forms such as SOPs, Analytical Test Methods and deviations
• Enter and update ATM information into laboratory databases for scientist use
• Verify all materials and information needed to compile or review the report are provided and promptly notifying document requester about need for additional information, material, or clarification
• Create and maintain proper network directory structure for the storage and archival of document files
• Enter information from study proposals into database for clinic and laboratory use.

What you will bring to the role

• Advanced computer skills, including working knowledge of Microsoft Office products
• Ability to interact effectively with superiors, peers, and other employees
• Ability to coordinate multiple projects and have the flexibility needed to adjust to changing priorities and unforeseen events
• Ability to use logical inferences to understand the “big picture” and long-term implications of these issues.
• Excellent oral and written skills
• Ability to prioritize work and define steps needed to achieve assigned project goals

Your experience

• Bachelor’s degree, with a scientific focus, and 0 -2 years of relevant work experience required.
• Experience in editing, regulatory affairs, clinical research, science, or other relevant area preferred

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 pageat www.worldwide.com/careers!

Job Type: Full-time

Benefits:

• 401(k)
• Dental insurance
• Health insurance
• Paid time off
• Vision insurance

Schedule:

• 8 hour shift
• Monday to Friday

Education:

• Bachelor's (Required)

Experience:

• Editing: 1 year (Preferred)
• Microsoft Office: 1 year (Preferred)
• Clinical research: 1 year (Preferred)
• handling scientific documentation: 2 years (Preferred)

Work Location: In person