Research Associate 1 IN OFFICE SAN ANTONIO, TX

About the position

The Research Associate 1 at Worldwide Clinical Trials is responsible for conducting screening visits for participant recruitment into clinical trials under the supervision of the Screening Supervisor. This role involves reviewing study protocols and informed consent forms for assigned studies, ensuring the accuracy of electronic and paper source documents according to study-specific protocols, and preparing and maintaining study-specific screening documents and folders. The Research Associate 1 serves as the primary contact for participants from screening through check-in for studies, addressing all questions related to study eligibility, participation, and concerns.

Responsibilities

• 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.

Requirements

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