Research Associate

We are currently seeking a Research Associate to join our diverse and dynamic team at ICON at our San Antonio TX site in a PRN (as needed) capacity. The Research Associate will coordinate with the CRC/Study Manager to ensure execution of all clinical study protocol activities within Good Clinical Practice (GCP) and Food Drug and Administration (FDA) regulations and requirements, sponsor expectations and ICON Development Solutions. Additionally, The RA has a basic understanding of research methods and various research study designs to identify and ensure successful clinical studies preparation and execution of studies.   

Title: Research Associate

Job Type: PRN (as needed)

Location: 100% on site - San Antonio TX

What you will be doing:

• Recognize, exemplify and adhere to ICON's values which centers around our commitment to People, Clients and Performance.

• As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.

• Familiarize, understand and apply all SOPs applicable to job description.

• Ability to understand protocol requirements.

• Participate in the early planning phases of clinical study by providing assistance to the CRC./Study Manager

• Assist in preparation of study source document charts, screening packets, maintain clinical study enrollment logs, payment and tracking logs, assist in filing of study documents, assists in query resolutions.

• Assist in admit set up (prepare arm bands, room assignments, coordinate training with clinical staff).

• Attend initiation meetings with study assigned CRC or Study Manager

• Assist with set up for Study Team Meetings to include (pre-study, SIV, mock runs and staff training).

• Assist with quality checks on source documents.

• Assist with phone contacts to subjects.

• Assist with review of screening charts to assure that all required results have been filed and verify that subject qualifies for enrollment.

• Participate in sponsor and monitor visits as required by the CRC or Study Manager

• To undertake other reasonably related duties as may be assigned from time to time from the CRC,  Study Manager,  Manager of Study Management, Director of Operations, and Principle/Sub Investigators.

Your profile:

• High School Diploma required
• 1 year relevant experience preferred, but not required