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Part Time Clinical Research Monitor Jobs in Edison, NJ

Adams Clinical

Lead Dosing Session Monitor

New York, NY · Hybrid

$60 - $70/hr

Job Role We are seeking a Part-Time Psychedelic Dosing Monitor / Therapist to support clinical trials focused on psychedelic research for individuals with depression, anxiety, and other mood ...

Adams Clinical

Lead Dosing Session Monitor

New York, NY · On-site

$60 - $70/hr

Job Role We are seeking a Part-Time Psychedelic Dosing Monitor / Therapist to support clinical trials focused on psychedelic research for individuals with depression, anxiety, and other mood ...

IQVIA

Clinical Trial Psych Rater

New York, NY · Remote

$62K - $156K/yr

Minimum 3 years administering scales in clinical research trials (excluding graduate/doctoral ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

IQVIA

Clinical Trial Psych Rater

New Providence, NJ · Remote

$62K - $156K/yr

Minimum 3 years administering scales in clinical research trials (excluding graduate/doctoral ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

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All JobsClinical Research Monitor JobsPart Time Clinical Research Monitor JobsPart Time Clinical Research Monitor Jobs in Edison, NJ

Part Time Clinical Research Monitor information

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$5

$41

How much do part time clinical research monitor jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for part time clinical research monitor in Edison, NJ is $40.07, according to ZipRecruiter salary data. Most workers in this role earn between $39.57 and $40.58 per hour, depending on experience, location, and employer.

What is a part time clinical research monitor?

Part time clinical research monitors are professionals who oversee the conduct of clinical trials on a part-time basis. Their primary role is to ensure that research studies comply with regulatory standards, protocols, and ethical guidelines while monitoring participant safety and data integrity. They may visit research sites, review documentation, verify data accuracy, and communicate with investigators, but work fewer hours than full-time monitors. This role is ideal for individuals seeking flexible schedules or supplementary income in the clinical research field.

How do part time clinical research monitors balance workload and ensure data quality across multiple studies?

Part-time clinical research monitors often manage their time across several studies by prioritizing tasks, maintaining clear communication with site staff, and using detailed tracking systems. They may face challenges in staying updated on protocol amendments and ensuring timely site visits due to limited hours. To maintain data quality, they frequently collaborate with full-time monitors, utilize remote monitoring tools, and keep thorough documentation. Regular check-ins with the research team help address any issues promptly and ensure compliance with regulatory standards.

What are the key skills and qualifications needed to thrive as a part time clinical research monitor?

To thrive as a Part Time Clinical Research Monitor, you need a solid understanding of clinical trial protocols, GCP guidelines, and typically a degree in a health-related field. Familiarity with electronic data capture (EDC) systems, regulatory documentation, and possibly certifications like ACRP or SOCRA is advantageous. Strong attention to detail, effective communication, and organizational skills help you manage site visits and collaborate with research teams. These skills ensure protocol compliance, data integrity, and the ethical conduct of clinical studies.

What is the difference between Part Time Clinical Research Monitor vs Part Time Clinical Trial Coordinator?

AspectPart Time Clinical Research MonitorPart Time Clinical Trial Coordinator
CredentialsTypically requires life sciences degree, certification (e.g., CCRP), and monitoring experienceUsually requires a degree in health sciences or related field, with project management skills
Work EnvironmentMonitors clinical sites remotely or on-site, ensuring compliance with protocolsCoordinates trial activities, manages documentation, and communicates with sites and sponsors
Employer & Industry UsageCommonly employed by CROs, pharmaceutical companies, and research institutionsEmployed by research sites, hospitals, or sponsors to oversee trial logistics

While both roles support clinical trials, the Part Time Clinical Research Monitor focuses on compliance and monitoring site activities, whereas the Part Time Clinical Trial Coordinator manages trial logistics and documentation. Understanding these differences helps in choosing the right career path or job search focus.

What are the most commonly searched types of Clinical Research Monitor jobs in Edison, NJ?

The most popular types of Clinical Research Monitor jobs in Edison, NJ are:

What are popular job titles related to Part Time Clinical Research Monitor jobs in Edison, NJ?

For Part Time Clinical Research Monitor jobs in Edison, NJ, the most frequently searched job titles are:

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The top searched job categories for Part Time Clinical Research Monitor jobs in Edison, NJ are:

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Part Time Clinical Research Monitor jobs near you

Psychiatrist / Sub-Investigator - Clinical Research (Part-Time, NYC)

Fieve Clinical Research

New York, NY

$100 - $200/hr

Full-time, Part-time

Posted 5 days ago

Job description

Fieve Clinical Research is seeking a second board-certified physician to serve as Sub-Investigator (Sub-I) or Co-Principal Investigator on active and upcoming Phase II-IV clinical trials in psychiatry and neurology. This is an ideal fit for a psychiatrist, neurologist, or internist - including residents, academic faculty, or clinicians transitioning from industry - who wants to stay connected to drug development without a full-time research commitment.

About Us Founded on the legacy of Ronald R. Fieve, MD - the Columbia University psychiatrist who established lithium therapy for bipolar disorder in the U.S. - Fieve Clinical Research has been part of Manhattan's clinical research landscape for more than 40 years. Our investigators have conducted 125+ trials across psychiatry, neurology, pain management, and internal medicine, working with major pharmaceutical sponsors and leading CROs including IQVIA and ICON.

What You'll Do

  • Serve as Sub-I or Co-PI on industry-sponsored outpatient trials (MDD, GAD, TRD, PTSD, migraine, fibromyalgia, and more)

  • Conduct protocol-specified medical/psychiatric evaluations and administer validated rating scales (MADRS, HAM-D, CGI, MIDAS, HIT-6)

  • Review subject eligibility, informed consent, and safety decisions

  • Identify and report adverse events per FDA/ICH-GCP requirements

  • Maintain GCP-compliant source documentation

  • Participate in site initiation visits, monitoring visits, and audits as assigned

  • Partner with the PI and Site Director on feasibility and enrollment strategy

  • Provide mentorship to study coordinators as your involvement grows

Why This Role

  • Minimum 1 day/week, Saturdays available - built around your existing clinical or academic schedule

  • No prior research experience required - we provide GCP training and mentorship

  • Authorship and CV-building potential on active industry trials

  • Direct path into psychopharmacology research at a site with a 40-year track record

Qualifications - Required

  • MD or DO from an accredited medical school

  • Active, unrestricted New York State medical license

  • Board certified or board eligible (NY) in Psychiatry, Neurology, or a closely related specialty; internists also considered

  • Ability to commit to a minimum of 1 on-site day/week in Midtown Manhattan

  • Baseline familiarity with clinical trial regulatory requirements (FDA, IRB, informed consent)

  • ICH-GCP certification preferred but not required - we support training/renewal

Qualifications - Preferred

  • 1-3+ years as a sub-investigator or investigator on industry-sponsored trials (not required - training provided)

  • Experience with MDD, bipolar disorder, schizophrenia, migraine, or epilepsy

  • Existing DEA registration, or willingness to obtain

  • Spanish language proficiency

  • Familiarity with EDC systems (Medidata Rave, Oracle InForm, REDCap)

Fieve Clinical Research is an Equal Opportunity Employer. All qualified applicants will receive consideration regardless of race, color, religion, sex, national origin, disability, or veteran status.

HOW TO APPLY

Please send your CV/biosketch, a brief cover note on your research background and therapeutic interests, and confirmation of your NY license/board status to:

Liana Slater, Operations - liana.slater@fieveclinical.com (347) 281-3998 | fieveclinicalresearch.com

Compensation Information:
$100.00 / Hourly - $200.00 / Hourly

Apply