Clinical Research Coordinator I Auzmer Research is seeking a motivated and detail-oriented Clinical Research Coordinator I (CRC I) to support and coordinate investigational medication trials aimed at improving patients' lives. This role offers a unique opportunity to work directly with patients while contributing to research that helps bring new treatments to market. As a Clinical Research Coordinator I, you will play a key role in supporting study activities, collecting and managing clinical data, and ensuring studies are conducted in compliance with regulatory and protocol requirements. This is a highly rewarding position that allows you to build long-term relationships with patients and follow their progress throughout their participation in a study. Auzmer Research is a rapidly growing clinical research site, and we are looking for someone who shares our passion for high-quality, patient-centered research. This position is also an excellent opportunity for pre-medical or healthcare-focused candidates to gain hands-on experience working closely with Principal Investigators and experienced research professionals in a clinical research setting.
Schedule:
Full-time, Monday through Friday, 8:00 AM - 5:00 PM In-person -
NO Remote Alternative Ideal Candidate:
Background or experience in biology, healthcare, or a related field (through school or work) Positive attitude, strong organizational and multitasking skills Excellent interpersonal and communication skills Strong desire to learn and grow in the clinical research field Demonstrated responsibility and professionalism CCRC eligibility and/or phlebotomy experience preferred, but not required
Key Responsibilities:
Develop and maintain a working knowledge of assigned study protocols, including visit schedules, procedures, laboratory requirements, informed consent, and investigational product accountability Perform study activities in compliance with Good Clinical Practice (GCP), federal regulations, and sponsor requirements Assist with patient recruitment and pre-screening activities, including reviewing medical history, discussing study opportunities with potential participants, obtaining records when appropriate, and determining preliminary eligibility based on protocol requirements. Ensure accuracy and completeness of study documentation, including eligibility checklists, source documents, drug accountability logs, screening logs, and study correspondence Work closely with the Principal Investigator and study team to ensure participants receive appropriate medical evaluation and care Educate and communicate with patients, families, and the community regarding clinical trials Promptly report adverse events and serious adverse events to the Principal Investigator and Research Management and assist with proper documentation and reporting Attend study-related training sessions, investigator meetings, and site initiation visits Support day-to-day study operations and patient visits
Training:
Training for this role is provided on-site
Job Type:
Full-time Pay:
$50,000.00 - $53,000.00 per year
Benefits:
401(k) 401(k) matching Dental insurance Health insurance Paid time off Vision insurance Application Question(s): Please note that relocation expenses are not reimbursed. If you currently reside in a different state, please indicate WHEN and WHERE in FL you plan to relocate. (If not applicable, write N/A.) Are you located in or around Lakeland, FL 33813?
Education:
Bachelor's (Required)
Experience:
Clinical trials: 1 year (Preferred) Patient care: 1 year (Preferred) Shift availability: Day Shift (Required) Ability to
