Site Research Assistant - Santa Ana, CA

Are you looking for an opportunity in Clinical Research?Do you want to work for an industry leading company that offers you an excellent benefits package and supports career progression whilst giving you the option of working flexibly? If so, come and join us - IQVIA are looking Clinical Research Assistant.

This role has an immediate start working 10 hours to start a week and building to 24 hours/week as recruitment builds for a period of 6 months to support the site. Some key aspects of the job will be to have prior clinical research experience - this will be onsite with EDC entry query resolution QC. Review/prescreen charts from EHR prescreen media referrals visit scheduling and reminders. Mental Health experience is preferred.

As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical trials and assist with collecting patient data.

Day to day responsibilities will include:

• Verifying and/or correcting research study information on source documents; researching queries and variances; providing feedback to the site data collector

• Accurate input of trial data into the Electronic Data Capture (EDC) system and tracking visits and procedures completed against budget in the clinical trial management system (CTMS)

• Preparing and maintaining study files, and timely submission of information

• Collecting, submitting and assisting in maintaining relevant regulatory and ethics documents

• Scheduling visits with research subjects, generating appropriate reports and documentation

• Other administrative support functions such as reception, office organization and supply management.

We are looking for candidates with the following skills and experience:

• BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g. clinical research coordinator, nurse, medical assistant, other medical profession

• Basic knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules

• Basic knowledge of medical terminology

• Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word

• Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and client

• ​Good organizational skills with the ability to pay close attention to detail.

#LI-CES and #LI-DNP

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world.  https://

We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities.

IQVIA’s ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding COVID-19 vaccination status.

The potential base pay range for this role is $25.00-$39.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.