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

Catholic Health

Research Coordinator

Roslyn, NY · On-site

$32 - $50/hr

Working collaboratively with investigators, research nurses, physicians, sponsors, and hospital departments, this role supports all phases of clinical research, including study start-up, subject ...

Catholic Health

Research Coordinator

Roslyn, NY · On-site

Working collaboratively with investigators, research nurses, physicians, sponsors, and hospital departments, this role supports all phases of clinical research, including study start-up, subject ...

Catholic Health

Research Coordinator

Roslyn, NY

Working collaboratively with investigators, research nurses, physicians, sponsors, and hospital departments, this role supports all phases of clinical research, including study start-up, subject ...

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Showing results 21-40

All JobsStudy Start Up Associate JobsStudy Start Up Associate Jobs in Newark, NJ

Study Start Up Associate information

See Newark, NJ salary details

$13

$32

$57

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

As of Sep 7, 2026, the average hourly pay for study start up associate in Newark, NJ is $32.98, according to ZipRecruiter salary data. Most workers in this role earn between $22.12 and $43.51 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.

What are popular job titles related to Study Start Up Associate jobs in Newark, NJ?

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What cities near Newark, NJ are hiring for Study Start Up Associate jobs?

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Study Start Up Associate jobs near you
Infographic showing various Study Start Up Associate job openings in Newark, NJ as of August 2026, with employment types broken down into 1% As Needed, 66% Full Time, 14% Part Time, and 19% Contract. Highlights an 89% Physical, 2% Hybrid, and 9% Remote job distribution, with an average salary of $68,603 per year, or $33 per hour.

ASSISTANT DIRECTOR FINANCE (JR227699)

Montefiore

Bronx, NY • On-site

Full-time

Re-posted 8 days ago

Job description

IntroductionTo heal, to teach, to discover and to advance the health of the communities we serve.

To learn more about the “Montefiore Difference” – who we are at Montefiore and all that we have to offer our associates, please click here. 

OverviewUnder the direction of the Sr. Director of Cancer Clinical Research Administration, the Assistant Director of Finance is responsible for the development, coordination and submission of Medicare Coverage Analyses, clinical trial budgets; preparing detailed cost assessments for industry sponsored clinical trials and investigator-initialed studies, including studies support by foundations and grants. 

Responsibilities

This position will collaborate with Program Directors to oversee clinical research billing compliance for oncology studies ensuring compliance with local, state and federal regulations. This position will be responsible for the reconciliation of clinical research accounts. 

This position will collaborate with the Assistant Director of Regulatory Affairs to monitor and track Time to Activation of study start-up. This position will interact on a regular basis with faculty, research nurses, study coordinators, departmental offices, outside sponsors, and other relevant staff.

Requirements

  • Master's degree required in life science, public health, or business administration 

  • Minimum of 5 years related work experience with clinical trial budget development and negotiations

  • ACRP or SOCRA required within 24 months of employment 

  • Working knowledge of local, state, federal and international government codes/regulations related to the conduct of human subject research and CMS guidelines

  • Extensive experience with CTMS and other clinical trial electronic systems (CTMS, EPIC, VELOS, COMPLION) are highly desirable

  • Exceptional communication, analytical, presentation and time management skills

Apply