Site Research Assistant - Miami, FL
About The Position
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. 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.
Requirements
- Minimum of an associate’s degree or equivalent education and experience.
- 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.
- Please note: This position is not eligible for sponsorship.
Nice To Haves
- At least 1 year of experience in a clinical research setting (preferred).
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.
- Must be able/comfortable doing community outreach, pre-screening/recruitment, and EDC entry.
- Ability to support additional administrative tasks as needed.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Part-time
Career Level
Entry Level
Education Level
Associate degree
