Clinical Research Coordinator I

DM Clinical Research; Phoenix (AZ); On-site; USD 50,000 - 70,000; Full time

Job summary

A clinical research organization is seeking a Clinical Research Coordinator I in Phoenix, AZ. The role involves conducting study visits, documenting procedures, and managing data entry. Candidates must have at least one year as a Clinical Research Coordinator and two years of clinical research experience. A high school diploma is required, and ACRP certification is preferred. This position offers an opportunity to engage with research participants and contribute significantly to clinical trials.

Qualifications

• At least one year of experience as a Clinical Research Coordinator (CRC).
• At least two years of experience in a clinical research setting.
• ACRP or equivalent certification is preferred.

Responsibilities

• Conduct study subject visits and document procedures.
• Ensure adherence to ALCOA-C Standards.
• Complete data entry and query resolution.
• Participate in subject recruitment and retention efforts.
• Engage with research participants and address concerns.

Skills

Detail-oriented

Multi-tasking

Energetic

Goals-driven

Education

High School Diploma or equivalent

Foreign Medical Graduates

Job description

Position: Clinical Research Coordinator I

Location: Phoenix, AZ

Job Id:1154

# of Openings:2

Clinic Research Coordinator I

Duties & 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 & Experience

Education

• High School Diploma or equivalent required
• Foreign Medical Graduates preferred

Experience

• At least one year 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.