Clinical Research Coordinator

The Clinical Research Coordinator will manage the day-to-day operations of various research studies. The key responsibilities include obtaining informed consent, leading recruitment efforts, coordinating patient visits, performing blood draws and other clinical assessments, maintaining study documentation, ensuring protocol compliance, reporting adverse events, and collaborating with investigators, site staff, and study sponsors.

Required Qualifications:

• Bachelor's degree or equivalent experience in a related field (i.e., life sciences, healthcare, etc.)
• Experience in a clinical research and/or healthcare setting; Preference given to those with direct patient care experience (i.e., research coordinator, phlebotomist, medical assistant, nursing assistant, etc.)
• Demonstrated ability to organize and prioritize a complex and dynamic workload
• Critical thinker and problem solver with proven ability to take initiative and follow through on assignments with minimal supervision
• Ability to exercise discretion and sound judgment; High level of integrity and honesty in maintaining confidentiality
• Strong written and verbal communication skills; Ability to interact in a professional, resourceful, and courteous manner

Preferred Qualifications:

• Phlebotomy certification or recent experience independently performing blood draws
• Working knowledge of medical terminology, clinical research concepts and practices, and relevant policies and regulatory requirements
• Bilingual (Spanish/English) speaker

Primary Responsibilities:

• Support research efforts by providing comprehensive coordination for various Phase I-IV clinical trials in accordance with established research protocols and standard operating procedures (SOPs)
• Perform all duties in compliance with applicable laws, regulations, policies, and procedural requirements (FDA, ICH, GCP, HIPAA, IRB, IATA, etc.)
• Execute protocol-specified patient visits and procedures, which may include, but not limited to, vital signs, phlebotomy, injections, spirometry, ECG/EKG, etc.
• Handle, process, and prepare biological samples for shipment
• Ethically recruit qualified subjects to meet enrollment timelines; Create and disseminate study materials and advertisements for local recruitment campaigns
• Conduct all screening activities for assigned protocols, including assessing patient eligibility, educating patients on non-medical trial concepts and details; Assist investigator in the informed consent process

Job Type: Full-time

Pay: $ $32.00 per hour

Expected hours: 35 – 40 per week

Benefits:

• 401(k)
• 401(k) matching
• Health insurance
• Paid time off
• Retirement plan

Work Location: In person