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Part Time Medical Monitor Clinical Trial Jobs in Springfield, MA

Education: PhD or PsyD (Psychology, Psychiatry, Health Sciences), Medical Doctor (MD), Foreign ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

... clinical trial analysis, regulatory submission reviews, and observational study assessments ... academic medical contexts. * Demonstrated command of clinical study design, regulatory ...

Biostatistician

Hartford, CT · Remote

$60 - $100/hr

... clinical trial analysis, regulatory submission reviews, and observational study assessments ... academic medical contexts. * Demonstrated command of clinical study design, regulatory ...

... clinical trial analysis, regulatory submission reviews, and observational study assessments ... academic medical contexts. * Demonstrated command of clinical study design, regulatory ...

Biostatistician

Springfield, MA · Remote

$60 - $100/hr

... clinical trial analysis, regulatory submission reviews, and observational study assessments ... academic medical contexts. * Demonstrated command of clinical study design, regulatory ...

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Part Time Medical Monitor Clinical Trial information

See Springfield, MA salary details

$11

$37

$68

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

As of Aug 24, 2026, the average hourly pay for part time medical monitor clinical trial in Springfield, MA is $37.54, according to ZipRecruiter salary data. Most workers in this role earn between $25.62 and $47.88 per hour, depending on experience, location, and employer.

What is a part time medical monitor in a clinical trial?

A part time medical monitor in a clinical trial is a licensed physician who oversees the safety of participants and the integrity of clinical data, but does so without committing to a full-time schedule. They review adverse event reports, ensure the trial follows ethical guidelines, and provide medical expertise on patient safety issues as needed. Their flexible role allows them to support multiple studies or balance other professional responsibilities while still playing a critical part in clinical research.

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

To thrive as a Part Time Medical Monitor in a clinical trial, you need a medical degree (MD or equivalent), expertise in clinical research, and a strong understanding of Good Clinical Practice (GCP) guidelines. Familiarity with electronic data capture (EDC) systems, safety reporting platforms, and relevant certifications such as GCP training are typically required. Excellent attention to detail, critical thinking, and effective communication skills help you navigate complex safety issues and collaborate with multidisciplinary teams. These competencies are essential for ensuring patient safety, regulatory compliance, and the overall integrity of clinical trials.

What are some common challenges faced by part-time medical monitors in clinical trials?

Part-time Medical Monitors in clinical trials often face challenges related to balancing multiple responsibilities across different studies or employers. They must stay up-to-date with protocol changes, quickly review and respond to safety data, and ensure timely communication with study teams despite limited hours. Effective time management and clear communication are essential to coordinate with investigators, sponsors, and other stakeholders while maintaining compliance and participant safety. Adapting to varying team structures and trial phases can also require flexibility and strong organizational skills.

What are popular job titles related to Part Time Medical Monitor Clinical Trial jobs in Springfield, MA?

For Part Time Medical Monitor Clinical Trial jobs in Springfield, MA, the most frequently searched job titles are:

What job categories do people searching Part Time Medical Monitor Clinical Trial jobs in Springfield, MA look for?

The top searched job categories for Part Time Medical Monitor Clinical Trial jobs in Springfield, MA are:

What cities near Springfield, MA are hiring for Part Time Medical Monitor Clinical Trial jobs?

Cities near Springfield, MA with the most Part Time Medical Monitor Clinical Trial job openings:

Infographic showing various Part Time Medical Monitor Clinical Trial job openings in Springfield, MA as of August 2026, with employment types broken down into 100% Part Time. Highlights an 100% In-person job distribution, with an average salary of $78,073 per year, or $37.5 per hour.

Clinical Trial Rater

IQVIA

Springfield, MA • Remote

Part-time

Posted 7 days ago


IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

62nd of 225 rated it services


Job description

Clinical Trial Rater - Borderline Personality Disorder (BPD)

Location: Remote based in the US
Hours: Approximately 5h per week
Role: Clinical Specialist

Start: immediate

Contract based

About IQVIA

IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We collaborate with top pharmaceutical and biotech companies to accelerate innovation and improve patient outcomes. Our mission is to combine data science and human expertise to transform healthcare worldwide.

We are seeking experienced and reliable Clinical Trial Raters to conduct standardized psychiatric assessments for a clinical trial in Borderline Personality Disorder (BPD). The rater will be responsible for administering validated clinicianrated instruments, ensuring high-quality, consistent data collection in accordance with the study protocol, GCP, and regulatory requirements.

This role requires strong clinical judgment, experience with psychiatric populations, and the ability to maintain objectivity and interrater reliability across multiple assessments and time points.

Key Responsibilities
  • Conduct structured and semistructured clinical interviews with trial participants diagnosed with Borderline Personality Disorder
  • Administer, score, and document validated psychiatric rating scales: CGI-S, and CGI-C or CGIC-S
  • Maintain interrater reliability, including participation in calibration, training, and quality review sessions
  • Identify and escalate safety concerns (e.g. suicidality) according to protocol and sponsor guidelines
  • Work closely with study investigators, site staff, and sponsor/CRO teams to support highquality trial execution
  • Adhere to Good Clinical Practice (GCP), SOPs, and ethical guidelines at all times
  • Maintain participant confidentiality and a traumainformed, empathetic approach during all assessments
    Required Qualifications
    • Education: PhD or PsyD (Psychology, Psychiatry, Health Sciences), Medical Doctor (MD), Foreign Medical Doctor (FMD), or Doctor of Osteopathic Medicine (DO)
    • Licensure: Licensed Clinician:MD/FMD/DO, Psychiatrist, Clinical Psychologist,Psychotherapist, Mental Health Counselor/Practitioner(LMHC/LCMHC/LMHP)or Professional Counselor(LPC/LCPC/LPCC)
    • Clinical Experience: 3 years of clinical experience withBorderline Personality Disorder(BPD) population
    • Clinical Trial Rater Experience 3 years of experience as clinical trial rater, including semi-structured psychiatric assessments
    • 3 years of experience with Clinical Global Impression rating scales
      • Clinical Global Impression-Severity (CGI-S) and
      • Clinical Global Impression-Change (CGI-C) or
      • Clinical Global Impression-Change in Severity (CGIC-S)
    Why Work With Us?
    • Flexible, remote work schedule.
    • Opportunity to contribute to global clinical research.
    • Collaborate with a team committed to improving patient care and advancing science.

    #LI-DNP #LI-Remote #LI-HCPN

    IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com

    IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

    IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

    The potential base pay range for this role is The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

    What IQVIA employees say

    Pay

    Benefits

    Hours and flexibility

    Workplace

    Get the full story on Breakroom


    IQVIA logo

    About IQVIA

    Sourced by ZipRecruiter

    At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

    Industry

    Health care and social assistance

    Company size

    10,000+ Employees

    Headquarters location

    Durham, NC, US