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Clinical Study Associate Jobs in New Jersey (NOW HIRING)

Global Channel Management, Inc.

$57/hr

Candidates with a nursing diploma/assoc degree with substantial experience may be considered for ... Clinical Study Manager duties are: * Develop project cross-functional, integrated study plan to ...

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Clinical Study Associate information

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$12

$32

$56

How much do clinical study associate jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for clinical study associate in New Jersey is $32.02, according to ZipRecruiter salary data. Most workers in this role earn between $21.49 and $42.21 per hour, depending on experience, location, and employer.

What is a clinical study associate?

Clinical Study Associates (CSAs) are professionals who support the planning, execution, and monitoring of clinical trials in the pharmaceutical, biotechnology, or medical device industries. They help coordinate study logistics, maintain study documentation, and ensure compliance with regulatory requirements. CSAs often work closely with Clinical Research Associates, study coordinators, and investigators to ensure that trials are conducted according to protocol and timelines. Their role is essential in ensuring the accuracy and integrity of data collected during clinical research.

What are some common challenges clinical study associates face when managing multiple clinical trials simultaneously?

Clinical Study Associates often juggle several clinical trials at once, which can present challenges such as prioritizing competing deadlines, maintaining accurate documentation for each study, and ensuring consistent communication with cross-functional teams. Staying organized and proactive is essential, as unforeseen protocol amendments or site issues can arise. Building strong relationships with site staff and utilizing effective project management tools can help CSAs navigate these complexities and deliver high-quality results.

What are the key skills and qualifications needed to thrive as a clinical study associate, and why are they important?

To thrive as a Clinical Study Associate, you need a strong understanding of clinical research processes, regulatory requirements, and typically a life sciences degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification are commonly required. Attention to detail, organizational skills, and effective communication set top performers apart in this role. These competencies ensure accurate study documentation, regulatory compliance, and smooth coordination across research teams.

What is the difference between Clinical Study Associate vs Clinical Research Coordinator?

AspectClinical Study AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like CCRP or CCRA beneficialBachelor's degree in health sciences or related field; certifications like CCRP advantageous
Work EnvironmentPharmaceutical companies, CROs, clinical trial sitesHospitals, clinics, research centers
Job FocusMonitoring clinical trials, ensuring protocol compliance, data accuracyManaging daily trial activities, patient recruitment, data collection
Employer & Industry UsageCommonly employed in pharma and CROsPrimarily in healthcare and academic research settings

Both roles involve clinical trial oversight but differ in focus: Clinical Study Associates primarily monitor and ensure compliance during trials, while Clinical Research Coordinators manage daily trial operations and patient interactions. Understanding these distinctions helps in choosing the right career path or job search focus.

What are the most commonly searched types of Clinical Study jobs in New Jersey?

The most popular types of Clinical Study jobs in New Jersey are:

What cities in New Jersey are hiring for Clinical Study Associate jobs?

Cities in New Jersey with the most Clinical Study Associate job openings:

Clinical Study Associate jobs near you
Infographic showing various Clinical Study Associate job openings in New Jersey as of August 2026, with employment types broken down into 2% As Needed, 73% Full Time, 15% Part Time, 2% Temporary, and 8% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $66,603 per year, or $32 per hour.

Clinical Study Manager

Global Channel Management, Inc.

$57/hr

Contractor

Re-posted 14 days ago

Job description

Company Description

Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation.  Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function.  Organizations need to reduce training and labor costs but at same requiring the best "talent " for the job. 


Qualifications

Clinical Study Manager needs 5 years relevant experience is required with a BSc, 3 years with a MS/MPH, or 2 years with PharmD/PhD/MD


Clinical Study Manager requires:

  • Phase II/III Oncology trial experience strongly preferred
  • Global trial experience strongly preferred
  • Experience working in both sponsor and CRO organizations strongly preferred
  • Candidates with a nursing diploma/assoc degree with substantial experience may be considered for this position.
  • clinical
    or basic research in a Pharmaceutical company, a Medical
    device/Diagnostic company, Academic Research Organization (ARO) or
    Contract Research Organization (CRO). CRA experience is preferred. Time
    spent directly in a medical environment (e.g. as a Study Site
    Coordinator) is also considered relevant.

Clinical Study Manager duties are:


  • Develop
    project cross-functional, integrated study plan to study start up
    (in-house) and validate and manage to the overall study implementation
    plan provided by the CRO. Participate in site selection and site
    qualification with (study team and CRO).
  • Contribute to
    operational delivery aspects of the protocol and lead document review
    & coordination for the protocol and amendments.
  • Additional medical writing tasks may involve ICF, CRF guidelines, IB and safety communications, DSUR, IND.  
Additional Information

$57/hr

6 months

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About Global Channel Management

Sourced by ZipRecruiter

Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Global Channel Management understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function. Organizations need to reduce training and labor costs but at the same time requiring the best talent for the job. GCM's Ownership and Management teams have extensive Staffing, Recruiting, HR and Executive Leadership knowledge, Experience and Expertise. Our Understanding and Commitment to our Client's Satisfaction are key reasons GCM has been successful in establishing long term relationships.

Industry

Recruiting and staffing services

Company size

11 - 50 Employees

Headquarters location

Austell, GA, US

Social media

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