Site Research Assistant - Miami, FLWork Set‑Up: On‑site

Scheduled Weekly 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 leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation. Our teams combine deep scientific expertise with cutting‑edge technology to deliver high‑quality data and insights that shape the future of clinical trials.

Job Profile Summary

The Research Assistant plays a key role in supporting the conduct of clinical trial activities in accordance with all applicable regulations. Success in this role requires logical thinking, strong prioritization skills, adaptability in a fast‑paced environment, and excellent interpersonal and team‑building abilities.

Responsibilities

• Perform EDC data entry and query resolution.
• Develop strong working relationships and maintain effective communication with study team members.
• Collaborate with investigators and office staff to build trust and support clinical–research workflows.
• Assist with screening, pre‑screening referrals, recruiting, and enrolling research subjects.
• Manage patient/research participant scheduling and visit coordination.
• Collect participant history and coordinate follow‑up care and laboratory procedures.
• Adhere to IRB‑approved protocols and assist in the informed consent process.
• Promote participant safety and comply with protocol‑related requirements.
• Coordinate protocol‑related procedures, study visits, and follow‑up care.
• Comply with company and sponsor SOPs, guidelines, and regulatory expectations.
• Schedule subject visits and required protocol‑related procedures.

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 and the principles of Good Clinical Practice (GCP).
• Understanding of protocols, study‑specific procedures, consent forms, and study schedules.
• Skill in required clinical procedures and familiarity with medical terminology.
• Strong attention to detail and organizational ability.
• Ability to establish and maintain effective working relationships with coworkers, managers, physicians, patients, and clients.
• Applicable certifications and licenses as required by company, state, country, or regulatory bodies.
• Must be able/comfortable doing community outreach, pre‑screening/recruitment, and EDC entry.
• Ability to support additional administrative tasks as needed.Please note: This position is not eligible for sponsorship.

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# #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.