MD First Research Chandler LLC · 1 day ago
Clinical Research Coordinator
Chandler, AZ
Full-time
Onsite
Entry, Mid Level
2+ years expMD First Research Chandler LLC is seeking a detail-oriented and motivated Clinical Research Coordinator to manage and execute clinical trials in neurology. The role involves coordinating trial activities, ensuring compliance, and maintaining patient communication while contributing to advancements in healthcare.
Research
Responsibilities
Monitor clinical trial activities and maintain compliant documentation
Ensure adherence to ICH-GCP and protocol-specific procedures
Participate in training for new protocols and attend investigator meetings
Collaborate with the PI on IRB submissions, regulatory documents, and study material prep
Create, maintain, and organize study source documents, binders, and logs
Screen, and consent patients in line with study protocols
Conduct reminder calls and prepare exam rooms before visits
Perform vital signs, ECGs, and phlebotomy
Perform psychometric and cognitive assessments (training provided or preferred)
Maintain respectful, HIPAA-compliant patient communication and care
Accurately record findings in e-source and EDC systems (EDC experience required)
Answer sponsor queries and communicate with study monitors
Transfer any paper data from source to digital platforms (scanner, computer, etc.)
Maintain subject charts and enter participants into billing matrix
Process and ship lab samples per protocol
Monitor and reorder lab kits and supplies; track expiration dates
Maintain investigational product accountability logs if required
Qualification
Required
Candidates must live in the Phoenix metropolitan area
Experience in Neurology is preferred
Monitor clinical trial activities and maintain compliant documentation
Ensure adherence to ICH-GCP and protocol-specific procedures
Participate in training for new protocols and attend investigator meetings
Collaborate with the PI on IRB submissions, regulatory documents, and study material prep
Create, maintain, and organize study source documents, binders, and logs
Screen, and consent patients in line with study protocols
Conduct reminder calls and prepare exam rooms before visits
Perform vital signs, ECGs, and phlebotomy
Maintain respectful, HIPAA-compliant patient communication and care
Accurately record findings in e-source and EDC systems
Answer sponsor queries and communicate with study monitors
Transfer any paper data from source to digital platforms
Maintain subject charts and enter participants into billing matrix
Process and ship lab samples per protocol
Monitor and reorder lab kits and supplies; track expiration dates
Maintain investigational product accountability logs if required
Preferred
Bachelor's degree in life sciences or related field
2+ years of clinical research coordinator experience
RealTime CTMS experience preferred
Rater certification or psychometric testing experience preferred
Strong knowledge of GCP, HIPAA, and clinical trial workflows
Phlebotomy and sample processing skills
Exceptional communication, time management, and problem-solving abilities
Comfortable working with diverse populations including geriatric and neurologic patients
Benefits
401(k)
401(k) matching
Bonus based on performance
Company parties
Competitive salary
Dental insurance
Employee discounts
Health insurance
Opportunity for advancement
Paid time off
Vision insurance
Wellness resources
Company
MD First Research Chandler LLC
Welcome to MD First Research Chandler, where patient well-being and cutting-edge research intersect.
11-50 employees
Funding
Current Stage
Early StageCompany data provided by crunchbase