Senior Clinical Research Coordinator (Data & Site Ops)

Dm Clinical Research Group

Phoenix (AZ)

On-site

USD 90,000 - 120,000

Full time

14 days+

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Job summary

Dm Clinical Research Group in Phoenix, AZ seeks an experienced Clinical Research Supervisor to oversee site activities, ensure GCP compliance, and drive enrollment. You will train staff, monitor data quality, and coordinate with cross-functional teams to meet sponsor expectations.

Responsibilities include conducting subject visits, maintaining study documentation to ALCOA-C standards, and leading site readiness for regulatory inspections.

Qualifications

  • Minimum of 5 years experience in Clinical Research.
  • Supervisory experience preferred.
  • ACRP certification or equivalent preferred.
  • Excellent written and verbal communication in English; Spanish bilingualism preferred.
  • Bachelor's degree (or higher) preferred.

Responsibilities

  • Complete all required training (ICH-GCP, IATA, protocol training) in a timely manner.
  • Conduct and oversee study subject visits per protocol and document findings in a timely manner.
  • Maintain regulatory and study documents with ALCOA-C standards; ensure traceability.
  • Coordinate with Laboratory, Data, Administrative, Investigators, and Sponsor/CRO teams.
  • Support subject enrollment targets and study timelines at assigned sites.
  • Prepare for sponsor/CRO Investigator Meetings and conduct patient consent discussions.

Skills

Clinical Research
Regulatory knowledge
Leadership
Quality Assurance
Bi-lingual English/Spanish

Education

Bachelor's degree
ACRP Certification (preferred)

Job description

Dm Clinical Research Group in Phoenix, AZ seeks an experienced Clinical Research Supervisor to oversee site activities, ensure GCP compliance, and drive enrollment. You will train staff, monitor data quality, and coordinate with cross-functional teams to meet sponsor expectations.

Responsibilities include conducting subject visits, maintaining study documentation to ALCOA-C standards, and leading site readiness for regulatory inspections.

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