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.