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Binance

Investigations Specialist

Thoroughly analyze customer account data, on-chain and off-chain transactions, account ... These tools assist our recruitment team but do not replace human judgment. Final hiring decisions ...

Nomi Health

Associate Data Manager

Ann Arbor, MI · On-site

Perform high-level data investigations * Track and communicate effectively with internal and external stakeholders regarding issue identification and resolution * Assist in documentation of customer ...

NCD Agency LLC

Data Analyst

Dallas, TX · On-site

Use SQL in BigQuery to analyze data, investigate business questions, troubleshoot discrepancies ... Support operational analytics. * * Assist with analysis involving billing, eligibility, carrier ...

DM Clinical

Clinical Research Coordinator I (3932)

Phoenix, AZ · On-site

$23 - $30.50/hr

Liaising with Laboratory team, Data team, Administrative staff, Clinical Investigators, Research ... Registered Medical Assistant certification or equivalent is preferred Knowledge and Skills: * Be an ...

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Clinical Research Coordinator I

Clinical Research Coordinator I

DM Clinical Research

Phoenix, AZ

$24 - $32/hr

Full-time

Posted 22 days ago

Job description

Clinic Research Coordinator I
The Clinical Research Coordinator I, will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. The CRC I will also ensure study enrollment meets or exceeds Sponsors' expectations. To ensure company goals are achieved on a timely basis.
Duties amp; Responsibilities:
  • Completing all the DMCR-required training, including but not limited to ICH-GCP Certification and IATA Certification on a timely basis.
  • Completing all the relevant training prior to study-start and on a continued basis in a timely manner. This will include but is not limited to:
    • a. Sponsor-provided and IRB-approved Protocol Training
    • b. All relevant Protocol Amendments Training
    • c. Any study-specific Manuals Training, as applicable
    • d. Sponsor-specified EDC and/or IVRS and any other relevant Electronic Systems training.
  • Conducting study subject visits, and all other relevant protocol-required procedures and documenting these in a timely manner.
  • Adherence to ALCOA-C Standards with all the relevant clinical trial documentation.
  • Completing data entry and query resolution in a timely manner as per internal company guidelines and as per sponsor expectations.
  • Demonstration of appropriate and timely follow-up on the action items, at their respective sites.
  • Demonstrated understanding and implementation of Laboratory Manuals and protocol-specified laboratory procedures, storage, temperature monitoring, equipment calibration and laboratory kit inventory, under the direction of the Site/Study Management Team, for assigned protocols.
  • Liaising with Laboratory team, Data team, Administrative staff, Clinical Investigators, Research Participants and Sponsor/CRO representatives, under the direction of the Site/Study Management Team, for assigned protocols.
  • Submitting required administrative paperwork per company timelines.
  • Participating in subject recruitment and retention efforts.
  • Engaging with Research Participants and understanding their concerns.
  • Any other matters, as assigned by management.

Knowledge amp; Experience:
Education:
  • High School Diploma or equivalent required
  • Bachelor's degree a plus
  • Foreign Medical Graduates preferred
Experience:
  • At least one years of experience as a CRC, preferably with practice coordinating industry-sponsored vaccines in a private setting.
  • At least two years of experience as a research assistant, data coordinator, laboratory personnel, or equivalent experience in a clinical research setting
Credentials:
  • ACRP or equivalent certification is preferred
  • Registered Medical Assistant certification or equivalent is preferred
  • Knowledge and Skills:
  • Be an energetic, go-getter who is detail-oriented and can multi-task.
  • Be goals-driven while continuously maintaining quality.
  • Bilingual in Spanish is preferred

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