Job Description

What the Research Associate 1 does at Worldwide

The Research Associate 1, has have familiarity with processing and reviewing clinical documentation, interacting with participants, and accommodating competing priorities in a dynamic clinical research environment.

What you will do

• Conducts screening visits for participant recruitment into clinical trials under the supervision of the Screening Supervisor.
• Reviews study protocol and informed consent form for studies they are assigned to.
• Ensures electronic and paper source documents for the trial are accurate according to study specific protocol.
• Prepares and maintains study-specific screening documents and study folders.
• Responsible for reviewing the informed consent form, medical history, inclusion/exclusion criteria, and other study documents as required with participants to determine eligibility.
• Serves as primary contact for participants from screening through check-in for studies. Addresses all questions from participants related to study eligibility, study participation, and/or concerns

What you will bring to the role

• Excellent written and oral communication skills.
• Ability to understand complex written and oral instructions.
• Excellent attention to detail resulting in high-quality work.
• Exceptional organizational skills.
• Ability to set and meet deadlines.

Your experience

• Bachelor’s Degree (preferably in the field of Life Sciences or Health).
• Six months or more experience in health care.

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