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Benefits:
- 401(k)
- Bonus based on performance
- Dental insurance
- Health insurance
- Paid time off
- Vision insurance
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 and/or phlebotomy experience preferred, but not required
- Bilingual (English/Spanish) 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
Benefits:
- 401(k)
- 401(k) matching
- Dental insurance
- Health insurance
- Paid time off
- Vision insurance
Application Question(s):
- Do you currently live within commuting distance of Lakeland, FL, or do you have confirmed plans to relocate to the area within the next 30 days?
- 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.)
Education:
- Bachelor's (Required)
Experience:
- Clinical trials: 1 year (Preferred)
- Patient care: 1 year (Preferred)
Language:
- Spanish (Preferred)
Shift availability:
- Day Shift (Required)
Ability to Commute:
- Lakeland, FL 33813 (Required)
Work Location: In person
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