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Research Assistant III (Lab) (4116

Job in Phoenix, Maricopa County, Arizona, 85003, USA
Listing for: Dm Clinical Research Group
Full Time position
Listed on 2026-08-17
Job specializations:
  • Healthcare
    Clinical Research
Salary/Wage Range or Industry Benchmark: 42000 - 64000 USD Yearly USD 42000.00 64000.00 YEAR
Job Description & How to Apply Below
Position: Research Assistant III (Lab) (4116)

Job Details

Job Location:

Phoenix - Phoenix, AZ 85012

The Research Assistant III (Lab) will be responsible for assisting the clinical research staff in conducting clinical research trials.

DUTIES & RESPONSIBILITIES
  • Completing DMCR-required training, including GCP and IATA.
  • Maintaining a working knowledge of current FDA regulations, GCP/ICH guidelines, organizational SOPs, guidance documents, and study protocols.
  • Assisting in the collection and recording of patient data per Sponsor requirements via the respective EDC system.
  • Timely and accurately assist in collection, management, and shipment of subjects' samples, and/or specimens
  • Completing Sponsor-required training prior to study-start, including, but not limited to
    • Sponsor-provided and IRB-approved protocol
    • All amendments
    • Investigator Brochure
    • Sponsor-specified EDC and/or IVRS
  • This includes completing the above-mentioned training prior to any study-related procedures being conducted on that said protocol should the RA be added to a protocol post-study start.
  • Maintaining clear, concise, accurate, and legible records.
  • Being prepared for and available at all required company meetings and monitoring visits for their assigned protocols at their respective site(s).
  • Utilizing the most recent version of the Protocol, Informed Consent, and Investigator Brochures at their respective site(s).
  • Assisting in the compilation and organization of all regulatory and administrative binders for their assigned protocols at their respective site(s) upon initial receipt of and wherever applicable.
  • Assisting in the creation of source documents for their assigned protocols at their respective site(s).
  • Conducting patient visits.
  • Assisting in reporting Adverse and Serious Adverse Events to the appropriate authorities per Sponsor.
  • Assisting in addressing and resolving issues from internal/external audits and monitoring letters for all assigned protocols at their respective site(s) in a timely manner.
  • Assists with all other aspects of the study and conducts as needed.
  • Any other matters as assigned by management.
KNOWLEDGE & EXPERIENCE

Education:
  • High school diploma or equivalent required
Experience:
  • Prior experience in clinical research is not required but preferred
Credentials:
  • Phlebotomist certificate preferred
  • Medical Assistant Certification preferred
Knowledge &

Skills:
  • Knowledge of medical terminology required
  • Must be detail-oriented and demonstrate attention to detail
  • Excellent customer service skills
  • Excellent computer skills
Qualifications#J-18808-Ljbffr
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