Clinical Research Coordinator Job at MD First Research Chandler LLC, Chandler, AZ

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  • MD First Research Chandler LLC
  • Chandler, AZ

Job Description

Job Description

Job Description

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.

Were 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:

  • Bachelors 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 researchone trial, one patient at a time.

Job Tags

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