Clinical Research Coordinator - I

Benefits

Qualifications

• •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
• •Bachelor's (Required)
• •Day Shift (Required)
• •Lakeland, FL 33813 (Required)
• •5 more items(s)

Responsibilities

• •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
• •Full-time, Monday through Friday, 8:00 AM – 5:00 PM
• •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 for this role is provided on-site
• •12 more items(s)