Research Assistant III (Lab) (4116)

Dm Clinical Research Group; Phoenix (AZ); On-site; USD 42,000 - 64,000; Full time

Job summary

Dm Clinical Research Group seeks a Research Assistant III (Lab) to support clinical trials at our Phoenix site. You will assist clinical staff, manage data capture, collect and ship samples, and maintain regulatory binders using current SOPs and study protocols.

You will complete required training (GCP, IATA), stay current with FDA regulations, prepare source documents, and participate in sponsor monitoring visits. Strong attention to detail and solid computer skills are essential.

Qualifications

• High school diploma or equivalent required.
• Knowledge of medical terminology required.
• Must be detail-oriented and demonstrate attention to detail.
• Excellent customer service skills.
• Excellent computer skills.

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.
• 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).
• 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.

Skills

Medical terminology

Detail-oriented

Customer service skills

Computer skills

Education

High school diploma or equivalent

Phlebotomist certificate preferred

Medical Assistant Certification preferred

Job description

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