Who we are

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 3,000 professionals spans 60 countries. We are united in cause with our customers to improve the lives of patients through new and innovative therapies.

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 the Senior Scientific Associate, Study Coordination does

A Senior Scientific Associate, Study Coordination works under the guidance of the Head of Bioanalytical Study Management, assists Bioanalytical Study Management Team with the conduct of regulated and non-regulated studies. They assist with study management as directed by the Bioanalytical Study Management Team or other scientific staff. This individual is a fully capable worker in a regulated CRO, provides high quality results in a timely manner, and understands work process across various teams.

What you will do

• Assist with the review of data using scientific judgment regarding the quality and integrity of data and records associated with assigned studies
• Assist with communications with analysts and other personnel involved in conducting the studies
• Assist with conducting/ensuring the study is in accordance with applicable SOPs, GLPs, and protocols
• Assist in scheduling and coordinating to maintain the flow of assigned studies and tasks
• Ensure quality of deliverables including data, reports, and electronic files
• Assist in writing/preparing Analytical Test Methods, Sample Analysis Plans, reports, SOPs, protocols, and Validation Plans

What you will bring to the role

• Highly developed organizational and time management skills
• Ability to understand graphs, tables, charts, and perform calculations needed for the task, usually associated with 1-year on-the-job training
• Ability to report data and procedures orally and in writing
• Ability to prioritize work and define steps needed to achieve assigned project goals

Your experience

• Bachelor’s degree, with a scientific focus, and 2 – 5 years of relevant work experience required

Why Worldwide

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 www.worldwide.com/careers! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.

Job Type: Full-time

Benefits:

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

Schedule:

• 8 hour shift
• Day shift
• Monday to Friday

Education:

• Bachelor's (Required)

Experience:

• Laboratory: 2 years (Preferred)

Work Location: In person