Research Assistant, On-Site, Pleasant View, UT
About The Position
This is an on-site position in Salt Lake City, Utah 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. 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 https://jobs.iqvia.com 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. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $29,400.00 - $91,300.00. 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.
Requirements
- Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines
- 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
Responsibilities
- 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 organization, and Sponsor policies, standard operating procedures (SOPs) and guidelines
- Schedule subject visits and procedures
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
No Education Listed
