Site Research Assistant - Kenosha, WI job opportunity at IQVIA Holdings, Inc..

Home Jobs In United States Of America Tag: WI Site Research Assistant - Kenosha, WI position at IQVIA Holdings, Inc.


DatePosted 30+ Days Ago bot
IQVIA Holdings, Inc. Site Research Assistant - Kenosha, WI
Experience: 1-years
Pattern: part-time
Country:
apply Apply Now
Salary:
Status:

WI

Copy Link Report
degreeAssociate
loacation Kenosha, WI, United States Of America
loacation Kenosha, WI....United States Of America

Research Assistant Work Setup: On-site Scheduled Hours: 24 hours per week About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world’s leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation. Our team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials.   Job Summary The Research Assistant plays a critical role in supporting clinical trial activities in accordance with GCP, IRB, and all applicable regulatory requirements. This position requires strong attention to detail, the ability to prioritize in a fast‑paced environment, and excellent communication skills. Experience in cardiovascular studies and hands‑on familiarity with EDC entry, query resolution, and reviewing charts from site databases are highly valued. Key Responsibilities Perform EDC data entry and query resolution in a timely and accurate manner. Review patient charts and records from the site database to support protocol-required tasks. Build and maintain strong working relationships with investigators, clinical staff, and study teams. Assist in screening, recruiting, and enrolling research participants. Manage scheduling of participants, study visits, and protocol-related procedures. Collect participant history and coordinate laboratory requirements and follow-up care. Support the informed consent process , ensuring adherence to IRB‑approved protocols. Promote participant safety by following protocol guidelines and reporting requirements. Ensure compliance with Sponsor and company SOPs, policies, and regulatory guidelines. Qualifications Minimum of an Associate’s degree or equivalent education and experience. At least 1 year of experience in a clinical research setting (preferred). Working knowledge of clinical trials, GCP principles, and study-specific procedures. Familiarity with cardiovascular studies (preferred). Ability to perform required clinical procedures and understand medical terminology. High attention to detail and strong organizational skills. Ability to collaborate effectively with coworkers, physicians, patients, and study stakeholders. Certifications and licenses as required by company, state, country, or regulatory bodies. Note: This position is not eligible for sponsorship. #LI-CES #LI-DNP #LI-HCP #ONSITE 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 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.

Other Ai Matches

Sr. CRA 1 - Single Sponsor Dedicated Applicants are expected to have a solid experience in handling Job related tasks
Global Study Leadership - Clinical Lead - Applicants are expected to have a solid experience in handling Job related tasks
Business Development Director Applicants are expected to have a solid experience in handling Job related tasks
Senior Consultant - OneKey (Digital Marketing exp essential) - FTC - maternity cover Applicants are expected to have a solid experience in handling Job related tasks
Enfermera Educadora con experiencia en PSP Applicants are expected to have a solid experience in handling Job related tasks
Applications Devl Spec 2 Applicants are expected to have a solid experience in handling Job related tasks
Phlebotomist - Wales Applicants are expected to have a solid experience in handling Job related tasks
Certified Diabetes Educator (Bilingual) – West Region (PST) – Remote Applicants are expected to have a solid experience in handling Job related tasks
Sr Reference File Maintainer Assoc Applicants are expected to have a solid experience in handling Job related tasks
Medical Laboratory Assistant 1 Applicants are expected to have a solid experience in handling Job related tasks
MedTech Part Time Clinical Nurse Consultant – Cincinnati, OH Applicants are expected to have a solid experience in handling OH related tasks
Associate Data Science Director Applicants are expected to have a solid experience in handling Job related tasks
Biostatisticien principal FSP - Développement clinique précoce (PK) Applicants are expected to have a solid experience in handling Job related tasks
Sr Reference File Maintainer Assoc Applicants are expected to have a solid experience in handling Job related tasks
Business Systems Analyst Applicants are expected to have a solid experience in handling Job related tasks
Product Sppt Tech Advisor 2 Applicants are expected to have a solid experience in handling Job related tasks
Associate Director, Solutions Engineering, IQVIA Digital Applicants are expected to have a solid experience in handling Solutions Engineering, IQVIA Digital related tasks
Delegad@ AP-Almería Applicants are expected to have a solid experience in handling Job related tasks
Associate Telecommunications Director Applicants are expected to have a solid experience in handling Job related tasks
Sr Reg Doc Coord Applicants are expected to have a solid experience in handling Job related tasks
Payroll Internship Applicants are expected to have a solid experience in handling Job related tasks
Freelance- Translators/Linguists, Thai into English Applicants are expected to have a solid experience in handling Thai into English related tasks
Principal Enterprise Architect (Remote) Applicants are expected to have a solid experience in handling Job related tasks