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Full Time Clinical Research Rater Jobs in Edison, NJ

THE ROLE We are seeking an experienced Clinical Research Nurse to join our team as a full-time Vitalief employee. In this role, you will support one of our clients who is an outpatient cancer center ...

THE ROLE We are seeking an experienced Clinical Research Nurse to join our team as a full-time Vitalief employee. In this role, you will support one of our clients who is an outpatient cancer center ...

Clinical Research Coordinator

Newark, NJ · On-site

$65K - $78K/yr

We are seeking an experienced Clinical Research Coordinator (CRC) to join Vitalief as a full-time employee with comprehensive benefits. This position will support a long-term observational vascular ...

We are seeking an experienced Clinical Research Coordinator (CRC) to join Vitalief as a full-time employee with comprehensive benefits. This position will support a long-term observational vascular ...

Clinical Nephrologist

New York, NY · On-site

$278K - $279K/yr

Mount Sinai Morningside and West is seeking a full-time Clinical Nephrologist at the Assistant ... Engage in clinical research. * Deliver outstanding clinical care in all aspects of Nephrology. * Be ...

Clinical Research Assistant

New York, NY · On-site

$23.35 - $35.51/hr

Emp Status Regular Full time Work Shift Compensation Range The base pay scale for this position is ... between the clinicians, research staff, and other research assistants. Provide overall ...

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Full Time Clinical Research Rater information

See Edison, NJ salary details

$8

$23

$47

How much do full time clinical research rater jobs pay per hour?

As of Aug 29, 2026, the average hourly pay for full time clinical research rater in Edison, NJ is $23.51, according to ZipRecruiter salary data. Most workers in this role earn between $17.93 and $26.88 per hour, depending on experience, location, and employer.

What is a full time clinical research rater?

Full Time Clinical Research Raters are professionals who assess and document the progress, symptoms, and responses of patients participating in clinical research studies. They use standardized rating scales, interviews, and questionnaires to collect accurate data that helps determine the effectiveness and safety of new treatments or interventions. These raters play a vital role in ensuring the integrity and quality of clinical trial data, often working closely with clinicians, researchers, and study coordinators. Their responsibilities also include adhering to study protocols, maintaining patient confidentiality, and ensuring compliance with regulatory standards.

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

Success as a Full Time Clinical Research Rater requires a background in psychology, neuroscience, or a related field, along with experience in clinical assessments and data collection. Familiarity with standardized rating scales, clinical trial databases, and regulatory compliance systems like Good Clinical Practice (GCP) certification is typically expected. Strong attention to detail, interpersonal communication, and objective judgment are crucial soft skills for accurate participant evaluation and collaboration with research teams. These competencies ensure reliable data collection, regulatory adherence, and the integrity of clinical research outcomes.

What are some typical challenges a full time clinical research rater may encounter, and how can they be managed?

Full Time Clinical Research Raters often face challenges such as managing large volumes of patient assessments, maintaining objectivity during subjective ratings, and adhering to strict study protocols. Balancing accuracy with efficiency is key, especially when dealing with sensitive patient information and tight study timelines. Collaborating closely with investigators and other research staff, participating in regular trainings, and using standardized rating tools can help ensure consistency and reliability in data collection.

What is the difference between Full Time Clinical Research Rater vs Part Time Clinical Research Rater?

AspectFull Time Clinical Research RaterPart Time Clinical Research Rater
Work HoursTypically 35-40 hours per weekLess than 20 hours per week
CertificationsOften requires relevant healthcare or research certificationsMay require similar certifications but less emphasis
Work EnvironmentFull-time employment in research facilities or remotePart-time roles, flexible locations
Employer UsageMajor research organizations, pharmaceutical companiesFreelance or contract research organizations

The main difference between a Full Time Clinical Research Rater and a Part Time Clinical Research Rater lies in work hours, certification emphasis, and employment type. Full-time roles offer consistent hours and benefits, while part-time positions provide flexibility. Both roles involve evaluating clinical data, but full-time positions are more integrated into research teams.

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

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

What cities near Edison, NJ are hiring for Full Time Clinical Research Rater jobs?

Cities near Edison, NJ with the most Full Time Clinical Research Rater job openings:

Clinical Research Investigator (MD/DO)

DM Clinical Research

Jersey City, NJ

$48K - $49K/yr

Full-time

Re-posted 19 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 Jersey City, NJ. 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) - New Jersey
  • 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.