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 the PRN Data Coordinator does at Worldwide

The PRN Data Coordinator, is responsible for assuring that the source data captured during a clinical trial has been transcribed into the Case Report Form (CRF) with accuracy and that the data transcription has been completed in accordance with Good Clinical Practice guidelines. The PRN Data Coordinator works under the general supervision and guidance of the Senior Manager, Study Conduct.

What you will do

• Reviews study protocol for studies assigned.
• Ensure data from source documents for the trial are accurately reflected on the Case Report Form whether electronic or paper.
• Keep track of source documents being filed into subject folders.
• Assistance with reconciliation of study records for archive.
• Identifies problems or potential problems and reports them to his/her supervisor.
• Responsible for requesting, scheduling and attending any training required for this position.

What you will bring to the role

• Excellent written and oral communication skills.
• Ability to understand complex written and oral instructions.
• Basic computer knowledge and applications required for generation of business correspondence and entry of study data into an electronic Case Report Form.
• Strong interpersonal skills.
• Excellent attention to detail.
  Some knowledge of the clinical research process, including Good Clinical Practices.

Your experience

• Bachelor’s degree or associate Degree (preferably in the field of Life Sciences or Health), and/or experience in a phase I clinical environment.
• Preferred: Experience or class work in the health field.

At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace by providing transparent compensation.

The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates):

The salary range provided is intended to give candidates an understanding of potential earnings. Compensation will fall within the provided range, and it not a guarantee of exact salary. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location. We ensure pay equity and transparency and comply with all applicable labor laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage.

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.