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. Experience in Neurology is preferred.

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. Candidates must live in the Phoenix metropolitan area.

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 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
  
  
  

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.