Clinical Research Coordinator - I

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 Commute:

• Lakeland, FL 33813 (Required)

Work Location: In person

Salary : $50,000 - $53,000