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Study Start Up Associate Jobs in Edison, NJ (NOW HIRING)

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Study Start Up Associate information

See Edison, NJ salary details

$13

$32

$57

How much do study start up associate jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for study start up associate in Edison, NJ is $32.65, according to ZipRecruiter salary data. Most workers in this role earn between $21.92 and $43.03 per hour, depending on experience, location, and employer.

What is the difference between Study Start Up Associate vs Clinical Trial Coordinator?

AspectStudy Start Up AssociateClinical Trial Coordinator
Required CredentialsBachelor's degree, knowledge of regulatory requirementsBachelor's degree, familiarity with clinical procedures
Work EnvironmentRegulatory and site initiation activitiesParticipant management and site coordination
Employer & Industry UsagePharmaceuticals, biotech, CROsHospitals, research centers, CROs

The Study Start Up Associate primarily focuses on regulatory submissions, site qualification, and initiation processes, ensuring trial readiness. In contrast, the Clinical Trial Coordinator manages participant recruitment, scheduling, and data collection. Both roles are essential in clinical research but differ in their core responsibilities and focus areas.

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Infographic showing various Study Start Up Associate job openings in Edison, NJ as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 15% Part Time, and 15% Contract. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $67,916 per year, or $32.7 per hour.

LAB TECHNOLOGIST SUPERVISOR

Zaddy Solutions

East Hanover, NJ • On-site

Other

Posted 9 days ago


Job description

Clinical Laboratory Scientist

Education and/or 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.

Essential Duties and Responsibilities:

  • Stays current with instrument capabilities and clinical trial regulations in order to provide input to clinical trial designs and execution.
  • Interacts with groups, such as, but not limited to CLSI, CLIA and CAP in order to ensure Stago is at the forefront of the market's evolution.
  • Works closely with counterparts to help conduct and support R&D activities as well as clinical trials in the US in facilitation of new Hematology and Hemostasis product launches.
  • Participates in the development of study protocols and ensures study designs are appropriate for execution in the lab.
  • Verify technical conditions prior to the start of a study, ensure instruments are in pristine working order and maintenance of equipment is up to date to ensure successful study conditions.
  • Utilizing local members of the service operations, create good logistical conditions for clinical studies to include but are not limited to delivery of reagents and/or instrument, specimens, exchange of correspondence, contracts and administrative documents.
  • Ensures full understanding of the protocol requirements to ensure the study proceeds efficiently in order to meet organizational time lines.
  • Works 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), ensures centralization and formatting of data from studies, as well as ensuring traceability of data.
  • Uses 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.
  • Assists 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.
  • Travel may be required for this position up to 10%, must be able to travel internationally.