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 40 hours a week for a period of 17 weeks 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. Focus will be on recruitment and community outreach.

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
• Bilingual Spanish/En
• 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 #HCP

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. Learn more at https://jobs.iqvia.com

We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe