ZipRecruiter

Log In

1

Contract Method Validation Jobs in Randolph, NJ (NOW HIRING)

LRSolutions

LABORATORY TECHNOLOGIST

Hackettstown, NJ · On-site

... instrument validations, correlations and training lab staff on new laboratory instrumentation ... Manages the Laboratory equipment service contracts and documentary elements of clinical trial ...

H. T. PROF Group

LABORATORY TECHNOLOGIST

Hackettstown, NJ · On-site

$65 - $85/hr

... instrument validations, correlations and training lab staff on new laboratory instrumentation ... Manages the Laboratory equipment service contracts and documentary elements of clinical trial ...

JobFormance

LABORATORY TECHNOLOGIST

Hackettstown, NJ · On-site

... instrument validations, correlations and training lab staff on new laboratory instrumentation ... Manages the Laboratory equipment service contracts and documentary elements of clinical trial ...

previous page

Showing results 41-60

All JobsContract Method Validation JobsContract Method Validation Jobs in Randolph, NJ

Contract Method Validation information

See Randolph, NJ salary details

$23

$53

$80

How much do contract method validation jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for contract method validation in Randolph, NJ is $53.44, according to ZipRecruiter salary data. Most workers in this role earn between $40.53 and $65.00 per hour, depending on experience, location, and employer.

What is the difference between Contract Method Validation vs Analytical Method Validation?

AspectContract Method ValidationAnalytical Method Validation
PurposeValidates that a contracted method meets specific requirements for a particular project or clientEnsures an analytical method is accurate, reliable, and reproducible for testing purposes
ScopeTypically project-specific, focusing on methods used under contractual agreementsBroader, covering method development, validation, and routine testing
CredentialsOften requires validation expertise, GMP knowledge, and industry-specific certificationsRequires analytical chemistry knowledge, validation experience, and relevant certifications
Work EnvironmentPharmaceutical, biotech, or manufacturing settings with client-specific projectsLaboratories performing routine testing and method development in similar industries

Contract Method Validation focuses on validating methods for specific client projects, while Analytical Method Validation ensures the overall reliability of testing methods used routinely in laboratories. Both roles require similar credentials and work in related environments, but their scope and purpose differ.

What cities near Randolph, NJ are hiring for Contract Method Validation jobs?

Cities near Randolph, NJ with the most Contract Method Validation job openings:

Contract Method Validation jobs near you

LABORATORY TECHNOLOGIST

Ron Sunshine Associates LLC

Hackettstown, NJ • On-site

Other

Posted 12 days ago

Job description

Laboratory Technologist

Education Experience:

B.S. Medical Technology/Clinical Laboratory Science or equivalent from an accredited four-year college or university required.

MT(ASCP) Certification or equivalent preferred.

Minimum five years experience in Hematology and Coagulation preferably, experience with instrument validations, correlations and training lab staff on new laboratory instrumentation.

Experience:

The Laboratory Technologist is involved with clinical trial regulations in order to provide input to clinical trial designs and execution. Assist in conducting and supporting R&D activities and clinical trials, in development of new Hematology and Hemostasis product launches. You will verify technical conditions prior to the start of a study. Working with members of the service operations team, create good logistical conditions for clinical studies, which include delivery of reagents and/or instrument, specimens, exchange of correspondence, contracts, and administrative documents.

Additional duties & requirements include:

  • Ensure full understanding of the protocol requirements to ensure the study proceeds efficiently in order to meet organizational time lines.
  • Work closely with the NCRA for all necessary study follow-up in accordance with defined procedure, including but not limited to the checklist for site initiation and monitoring visits, etc.
  • Ensure corrective actions are followed for proper conduct to freeze databases of results in accordance with the studies initial objectives.
  • Check completeness of records (all forms of media: paper and electronic), ensure centralization and formatting of data from studies, as well as ensuring traceability of data.
  • Use knowledge and experience with instrument validation, interference, on-board stability, Limit of Blank, Limit of Detection, Limit of quantification to perform Linearity and Method Comparison testing.
  • Maintain laboratory equipment following daily, weekly and monthly maintenance schedules as well as required quality control for all laboratory analyzers.
  • Participates in validation of new equipment as appropriate.
  • Assist the NCRA's in the development and maintenance of clinical study binders and utilization of eCRF.
  • Manages the Laboratory equipment service contracts and documentary elements of clinical trial activities;
  • Completes necessary clinical trial documentation from the site's perspective, in preparation of study start up.
  • Give scientific presentations as required.
  • Offer support on new product launches as needed.

Apply