Research Assistant, On-site, Rockville, MD
About The Position
This is a fully on-site position in Rockville, MD. Are you ready to accelerate your career in clinical research? Join Avacare, a dynamic Site Management Organization (SMO) where Clinical Research Coordinators (CRCs) gain unparalleled exposure to diverse trials, hands-on responsibilities, and a collaborative team environment. Why Avacare? At Avacare, CRCs wear more hats than in traditional research settings. You’ll gain experience across multiple therapeutic areas, manage complex protocols, and take ownership of key trial activities — from patient recruitment and informed consent to regulatory documentation and site audits. This breadth of responsibility not only strengthens your core CRC skills but also prepares you for future roles in clinical operations, monitoring, and beyond. Whether you're early in your CRC journey or ready to take the next step, Avacare offers a unique environment where your contributions matter and your career can flourish. 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. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
Requirements
- Hands-on experience in obtaining vital signs, performing phlebotomy, conducting ECGs, and processing lab specimens
- Solid understanding of site operations and the drug development process
- CRC I: Minimum of 1-3 years in clinical research setting at a clinical investigative site working with participants
- CRC II: Minimum of 3 years as a Clinical Research Coordinator in a clinical investigative site working with participants
- Strong written and verbal communication skills, with attention to detail and time management
- Comfortable using CTMS, eCRFs, and Microsoft Office tools
Responsibilities
- Manage 2–6 trials of varying complexity
- Perform clinical procedures
- Lead study coordination from start to finish
- Work closely with investigators, sponsors, and monitors
- Mentor junior staff
- Contribute to internal training
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
No Education Listed
