PRN Data Coordinator (US)
About The Position
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. 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 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.
Requirements
- 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.
Nice To Haves
- Experience or class work in the health field.
Responsibilities
- 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.
Benefits
- competitive benefits package depending on location
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What This Job Offers
Job Type
Part-time
Career Level
Mid Level
Education Level
Associate degree
