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System Integration Coordinator Jobs (NOW HIRING)

Panasonic

System Integration Engineer II

Lake Forest, CA · On-site

$82K - $138K/yr

The System Integration Engineer II is responsible for supporting the integration, installation ... Technical Coordination and Customer Support * Maintain effective working relationships with OEM ...

Apple Inc.

System Integration Lead

Austin, TX · On-site

System Firmware & Diagnostics Group has an immediate opening for a System Integration Lead. Our ... Providing coordination and leadership around debugging issues seen in the test suite. * Driving and ...

American Systems

$165K - $195K/yr

Support software and system configuration management, version alignment, environment coordination, and release integration planning. * Assist in troubleshooting and resolving complex integration ...

Apple

System Integration Lead

Austin, TX

$184K - $324K/yr

System Firmware & Diagnostics Group has an immediate opening for a System Integration Lead. Our ... Providing coordination and leadership around debugging issues seen in the test suite. Driving and ...

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How much do system integration coordinator jobs pay per year?

As of Sep 10, 2026, the average yearly pay for system integration coordinator in the United States is $76,706.00, according to ZipRecruiter salary data. Most workers in this role earn between $55,000.00 and $91,000.00 per year, depending on experience, location, and employer.

What are the most commonly searched types of System Integration jobs?

The most popular types of System Integration jobs are:

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For System Integration Coordinator jobs, the most frequently searched job titles are:

Site Development & Integration Coordinator

Houston, TX

DM Clinical Research
11 - 50 employees
Learn more about DM Clinical Researchexternal

Full-time

Re-posted 29 days ago

Job description

Site Development amp; Integration Coordinator
The Site Development amp; Integration Coordinator 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.
DUTIES amp; RESPONSIBILITIES
  • Completing all the relevant training prior to study-start and on a continued basis in a timely manner
  • Complete and implement Sponsor-provided and IRB-approved Protocol Training
  • All relevant Protocol Amendments Training or study-specific manual trainings
  • 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
  • Complete data reviews to ensure the highest standards of data integrity
  • Conduct training for site and SDI personnel
  • Sample processing, including PBMC samples
  • 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
  • DMCR-required training, including but not limited to ICH-GCP Certification and IATA Certification
  • 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
  • Flexibility with scheduling, including travel (50%) when required

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