Clinical Research Assistant

xperiences that far exceed traditional research roles. You will be involved in multiple therapeutic areas, manage intricate protocols, and take charge of key aspects of trials-from patient recruitment and obtaining informed consent to handling regulatory documentation and overseeing site audits. This diverse range of responsibilities not only enhances your core CRC skills but also positions you for future opportunities in clinical operations, monitoring, and other areas.

What You Will Discover:
• Diverse Skill Development: Manage 2-6 trials of various complexities, conduct clinical procedures, and coordinate studies from initiation to conclusion.
• Career Advancement: Collaborate closely with investigators, sponsors, and monitors while mentoring junior staff and contributing to training initiatives.
• Supportive Team Environment: Be part of a community that appreciates initiative, adaptability, and a commitment to ongoing learning.
• Global Reach: Experience the synergy of working within a local SMO backed by the extensive resources and influence of a global CRO.

Qualifications:
• Clinical Expertise: Practical experience in obtaining vital signs, performing phlebotomy, conducting ECGs, and processing lab specimens.
• Site Operations Acumen: Solid understanding of site operations and the drug development lifecycle.
• Experience:
• CRC I: At least 1-3 years in a clinical research setting at a clinical investigative site interfacing with participants.
• CRC II: Minimum of 3 years as a Clinical Research Coordinator in a clinical investigative environment working directly with participants.
• Communication & Documentation Skills: Exceptional written and verbal communication abilities, with a keen eye for detail and strong time management.
• Technical Skills: Proficient in using CTMS, eCRFs, and Microsoft Office applications.

Whether you are just starting your journey as a CRC or looking to elevate your career, Avacare offers a distinctive environment where your contributions are valued and your professional growth is prioritized.

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence in the life sciences and healthcare sectors. Our mission is to create intelligent connections to expedite the development and commercialization of innovative medical treatments, improving patient outcomes and population health worldwide.

IQVIA is committed to being an equal opportunity employer. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other protected status by applicable law.

The anticipated base pay range for this position is $29,400.00 - $73,400.00 annually. Actual base pay may vary based on factors including qualifications such as knowledge, skills, education, experience, location, and schedule (full or part-time). Depending on the position offered, additional compensation such as incentive plans, bonuses, and/or health and welfare benefits may be included.

At IQVIA, we seek out diverse talent with inquisitive minds and a steadfast commitment to innovation and impact. Regardless of your role, everyone at IQVIA contributes to our collective goal of enhancing the lives of patients globally. Thank you for considering a career with us.

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