Job Information
ICON Clinical Research Research Associate in San Antonio, Texas
Research Associate- ICON- San Antonio TX
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We are currently seeking a XXX 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
What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site (https://careers.iconplc.com/benefits) to read more about the benefits ICON offers.
ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here (https://careers.iconplc.com/reasonable-accommodations)
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here (https://wd3.myworkday.com/icon/d/task/1422$1235.htmld) to apply