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Laboratory Data Coordinator Jobs (NOW HIRING)

Colorado Psychiatric

Laboratory Supervisor

Denver, CO · On-site

Troubleshoots and resolves data inconsistencies. * 5. Prioritizes analytical work and process ... Coordinates and tracks service contracts for analytical equipment. Works with Procurement to ...

Metro Water Recovery

Laboratory Supervisor

Denver, CO · On-site

$86K - $120K/yr

Coli data used for regulatory compliance. Identifies areas for improved efficiencies and ... Coordinates and tracks service contracts for analytical equipment. Works with Procurement to ...

AOCUSA, Amalie Motor Oil

Laboratory Director

Vernon, CA · On-site

$185K - $205K/yr

... coordinates the maintenance of the laboratory data management system. * Provides technical consultation to operations staff in the evaluation and solution of problems where laboratory analysis is ...

AOCUSA

Laboratory Director

Vernon, CA · On-site

$185K - $205K/yr

... coordinates the maintenance of the laboratory data management system. * Provides technical consultation to operations staff in the evaluation and solution of problems where laboratory analysis is ...

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How much do laboratory data coordinator jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for laboratory data coordinator in the United States is $27.22, according to ZipRecruiter salary data. Most workers in this role earn between $21.15 and $32.21 per hour, depending on experience, location, and employer.

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Infographic showing various Laboratory Data Coordinator job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 11% Part Time, and 3% Contract. Highlights an 84% Physical, 4% Hybrid, and 12% Remote job distribution, with an average salary of $56,614 per year, or $27.2 per hour.

Site Development & Integration Coordinator

Houston, TX • On-site

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

Full-time

Re-posted 3 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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