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How much do clinical research rater jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for clinical research rater in Massachusetts is $24.80, according to ZipRecruiter salary data. Most workers in this role earn between $18.89 and $28.37 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the clinical research rater position?

To thrive as a Clinical Research Rater, you need a background in psychology, neuroscience, or a related health science field, with strong attention to detail and standardized assessment skills. Familiarity with clinical trial protocols, electronic data capture systems, and rating scales like the Hamilton Depression Rating Scale or PANSS is often required. Excellent observational, interpersonal, and communication skills help you accurately assess participants and collaborate with multidisciplinary research teams. These abilities ensure precise data collection and reporting, which are critical for the validity and success of clinical research studies.

What is a clinical research rater?

A Clinical Research Rater is responsible for administering standardized assessments and interviews to clinical trial participants to evaluate their cognitive, psychiatric, or neurological status. They work closely with investigators and study coordinators to ensure data accuracy and consistency in clinical trials. Raters must be trained in administering rating scales and maintaining objectivity in their evaluations. This role is critical in ensuring the integrity of clinical trial outcomes, especially in studies related to mental health, neurology, and other therapeutic areas.

What are some typical challenges faced by clinical research raters in their daily work?

Clinical Research Raters often face the challenge of maintaining objectivity and consistency while administering complex assessments across diverse participant populations. They must carefully follow study protocols, manage detailed documentation, and adapt to changes in trial requirements or participant schedules. Working closely with other research staff and clinicians requires strong communication and teamwork, especially when addressing discrepancies or unexpected findings. Staying up to date with assessment tools and best practices helps minimize errors and supports the integrity of the study data.

What are the most commonly searched types of Clinical Research Rater jobs in Massachusetts? The most popular types of Clinical Research Rater jobs in Massachusetts are:
What are popular job titles related to Clinical Research Rater jobs in Massachusetts? For Clinical Research Rater jobs in Massachusetts, the most frequently searched job titles are:
What job categories do people searching Clinical Research Rater jobs in Massachusetts look for? The top searched job categories for Clinical Research Rater jobs in Massachusetts are:
Clinical Research Rater jobs near you
Infographic showing various Clinical Research Rater job openings in Massachusetts as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $51,593 per year, or $24.8 per hour.

Clinical Research Investigator (MD/DO)

DM Clinical Research

Plymouth, MA

$50K - $51K/yr

Full-time

Re-posted 7 days ago

Job description

Clinical Research Investigator (MD/DO)
DM Clinical Research, the largest privately-owned research management organization in the Houston area and one of the top 50 in the country, is looking for an Investigator for our site in Boston, MA. This individual will conduct all clinical trials (studies) according to ICH, GCP, local regulations, study protocols, and company processes.
Responsibilities
  • Ensures the medical well-being and safety of the participants through the safe performance and execution of the studies.
  • Assists in maintaining clinical oversight and quality on the studies registered on and delivers on study targets, thereby contributing to the commercial success of the site.
  • Reviews enrollment progress, pre-screening and screening success rates, screen failure rates, safety, and retention of participants.
  • Interprets protocols and IB and participates in initiatives to strategize for patient recruitment.
  • Carries out clinical evaluation and assessment of participants to ensure eligibility to enroll in studies.
  • Ensures and protects the welfare and safety of participants through ethical conduct.
  • Fulfills and complies with all medical duties as per protocol, SOP/COP and ICH GCP and local regulations.
  • Exercises meticulous attention to detail in documentation and patient care.
Requirements
  • Medical license (MD, DO) - Boston
  • 2 years experience as a Clinical Research Investigator (Principal Investigator or Sub-Investigator)
  • Bilingual Spanish a plus
Flexible hours - schedule can be tailored as required.

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