Research Assistant, On-Site, Tempe, Arizona
Share
Job Location:
Monthly Salary:
Posted on:
16-10-2025
Vacancies:
1 Vacancy
Job Summary
This is a fully on-site position at the site in Tempe AZ
This is an exceptional opportunity for entry-level professionals aspiring to carve out a career in the dynamic field of clinical research. We are on the lookout for driven individuals who excel in teamwork and patient care. If you are comfortable in a clinical/patient care setting and are enthusiastic about propelling healthcare forward through clinical trials we would love to hear from you. While clinical skills such as obtaining patient vitals drawing blood and conducting EKGs are a plus they are not a prerequisite for this role.
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 clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity national origin disability status as a protected veteran or any other status protected by applicable law. potential base pay range for this role when annualized is $29400.00 - $73400.00. 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.
Key Skills
- Laboratory Experience
- Spss
- Data Collection
- DNA Isolation
- Stata
- Biochemistry
- Qualitative Research Interviewing
- Research Experience
- Statistical Software
- Molecular Biology
- Research Laboratory Experience
- Western Blot
About Company
IQVIA is the Human Data Science Company™. We are inspired by the industry we serve and provide solutions that enable life sciences companies to innovate with confidence, maximize opportunities and ultimately drive human health outcomes forward. Our approach is Human Data Science – a d ... View more
