This individual will play a key role in assisting in the conduct of clinical trial activities, in accordance with all applicable regulations governing the conduct of clinical trials. The primary skills include logical thinking, ability to prioritize, the ability to adapt quickly to changing business conditions, strong interpersonal and team building skills. Essential Functions: Develop strong working relationships and maintain effective communication with study team members Develop strong workin... more details
Title: Research Assistant, On-Site
This is a fully on-site position in (Colton, CA)
Overview:
This individual will play a key role in assisting in the conduct of clinical trial activities, in accordance with all applicable regulations governing the conduct of clinical trials. The primary skills include logical thinking, ability to prioritize, the ability to adapt quickly to changing business conditions, strong interpersonal and team building skills.
Essential Functions:
Develop strong working relationships and maintain effective communication with study team members
Develop strong working relationships with the investigators and office staff to build a foundation of trust and respect between the clinic and the research office
Assist with the screening, recruiting and enrollment of research subjects
Perform patient/research participant scheduling
Collect patient/research participant history
Data entry and Management
Coordinate follow-up care and laboratory procedures
Adhere to an IRB approved protocol
Assist in the informed consent process of research subjects
Support the safety of research subjects
Coordinate protocol related research procedures, study visits, and follow-up care
Comply with Avacare, and Sponsor policies, standard operating procedures (SOPs) and guidelines
Schedule subject visits and procedures
Required Knowledge Skills and Abilities:
Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines
Medical Terminology knowledge preferred
Clinical Skills preferred
Strong interpersonal skills with attention to detail a must
Demonstrated proficiency with word processing, spreadsheet, database, and presentation software (MS Office skills such as Outlook, Word, Excel, PowerPoint, SharePoint) and with clinical trial master filing systems.
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
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. https://jobs.iqvia.com/covid-19-vaccine-status
The potential base pay range for this role, when annualized, is $38,800.00 - $64,600.00. 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.
