Clinical Research Coordinator

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
  
  
  

Location: Chandler, AZ

Company: MD First Research Chandler, LLC

Schedule: Monday – Friday, 8:00 AM – 5:00 PM

Experience Preferred: RealTime CTMS, Rater Certification, Phlebotomy, EDC, Cognitive Assessments

Join Our Team:

Are you looking to make a real impact in clinical research? MD First Research Chandler is seeking a detail-oriented, motivated Clinical Research Coordinator (CRC) to help manage and execute a growing portfolio of cutting-edge clinical trials in neurology.

We’re looking for someone who values accuracy, patient safety, and the opportunity to contribute to meaningful advancements in healthcare. Our coordinators play a vital role in ensuring smooth trial operations from screening to close-out while working closely with investigators, patients, and sponsors.

Responsibilities:

You will be responsible for the full scope of coordinating clinical research trials, including:

Study Coordination & Compliance

• 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
  
  
  

Patient Management

• 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
  
  
  

Data & Documentation

• 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
  
  
  

Lab & Drug Accountability

• 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 Qualifications:

• Bachelor’s degree in life sciences or related field
• 2+ years of clinical research 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
  
  
  

What We Offer:

• Competitive compensation based on experience
• Structured onboarding and continuous professional development
• Access to a collaborative, supportive team and seasoned investigators
• A patient-first culture in a purpose-built research facility with onsite infusion and pharmacy services
  
  
  

Location:

3190 S. Gilbert Rd, Suite 5, Chandler, AZ 85286

Located in the East Valley, we serve a large, diverse adult and geriatric population, and maintain close hospital proximity for seamless care coordination.

Be part of our mission to improve lives through innovative research—one trial, one patient at a time.