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Full Time Clinical Research Rater Jobs in Columbus, OH

Battelle

Clinical Psychologist

Columbus, OH · On-site

$85.50K - $117.80K/yr

Job Summary The Health Research and Analytics (HRA) business line is seeking a highly motivated, full-time Clinical Psychologist to join our team in support of our government customer, U.S. Special ...

Battelle

Clinical Psychologist

Columbus, OH · Hybrid

$82.70K - $114K/yr

Job Summary The Health Research and Analytics (HRA) business line is seeking a highly motivated, full-time Clinical Psychologist to join our team in support of our government customer, U.S. Special ...

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

As of May 28, 2026, the average hourly pay for full time clinical research rater in Columbus, OH is $21.94, according to ZipRecruiter salary data. Most workers in this role earn between $16.73 and $25.10 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Full Time Clinical Research Rater, and why are they important?

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 are Full Time Clinical Research Raters?

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 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 Columbus, OH? The most popular types of Clinical Research Rater jobs in Columbus, OH are:
What are popular job titles related to Full Time Clinical Research Rater jobs in Columbus, OH? For Full Time Clinical Research Rater jobs in Columbus, OH, the most frequently searched job titles are:
What job categories do people searching Full Time Clinical Research Rater jobs in Columbus, OH look for? The top searched job categories for Full Time Clinical Research Rater jobs in Columbus, OH are:
What cities near Columbus, OH are hiring for Full Time Clinical Research Rater jobs? Cities near Columbus, OH with the most Full Time Clinical Research Rater job openings:
Full Time Clinical Research Rater jobs near you
Infographic showing various Full Time Clinical Research Rater job openings in Columbus, OH as of May 2026, with employment types broken down into 1% Locum Tenens, 1% As Needed, 80% Full Time, and 18% Part Time. Highlights an 85% Physical, 7% Hybrid, and 8% Remote job distribution, with an average salary of $45,630 per year, or $21.9 per hour.
Clinical Screening Coorinator

Clinical Screening Coorinator

Centricity Research

Columbus, OH • On-site

$23.50 - $31.25/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 7 days ago

Job description

Join Us at Centricity Research!
Centricity Research is one of the largest clinical research networks in North America. We are a fully centralized Integrated Research Organization (IRO) specializing in conducting Phase I-IV clinical trials in over 35 therapeutic areas: inpatient and outpatient; pharmaceutical, biotechnology, and medical device trials.
About the Role
We're looking for a Clinical Screening Coordinator to lead research-related recruitment initiatives and ensure the enrollment of high-quality patients in accordance with Centricity Research recruitment guidelines. In this role, your primary responsibility will be outreach / patient recruitment. In addition, you'll also screen patients for participation in clinical research studies with a solid understanding of study protocols, including inclusion/exclusion criteria, relevant medications, and medical conditions.
What You'll Do
  • Work on enrollment and retention initiatives with the Site Manager
  • Problem solve and create contingency plans to optimize enrollment via recruitment initiatives
  • Obtain and maintain computerized database of all ad callers
  • Return all phone calls/email responses to interested patients within 24 - 48 hours
  • Accurately complete recruitment tracking log and all applicable clinical trial management systems
  • Identify appropriate study candidacy based on knowledge of sites' recruiting and upcoming studies
  • Complete database query reviews for study candidacy and conduct outbound calls for study interest
  • Provide study metrics on a regular basis and provide ongoing feedback regarding outcome of recruitment initiatives
  • Occasionally attend community lectures, health fairs or events to promote Centricity Research
  • Promote clinical trials in the community through outreach events
  • Complete Informed Consent and screening visits per study protocol and Centricity Research SOP
  • Perform delegated tasks completely and accurately, including review of demographic information, medication history, medical history, obtaining vital signs (blood pressure, heart rate, temperature, and waist, weight, and height measurements
  • Complete the source documents, case report forms, and data queries in a timely manner, accurately, and completely.
  • Assist the Central Recruitment, Research Operations and/or Investigators with any other tasks as required
  • Able to work in a regional setting to support sites with recruitment and screening as needed

You Might Be a Great Fit If You:
  • Communicate clearly and comfortably with patients by phone, email, and in person
  • Stay organized and pay attention to details, especially when managing multiple tasks like outreach, documentation, and scheduling
  • Are curious about clinical research and excited to learn protocols, medical terminology, and research ethics
  • Feel confident using everyday computer tools like spreadsheets, databases, and email, and are open to learning systems like CTMS or EMR
  • Bring experience from a healthcare, research, or customer-facing role, or are ready to dive in and learn on the job

Why Centricity Research?
Our Mission
We connect people to scientific advancements through groundbreaking research within a deeply human experience.
Our Core Values
  • Quality: We aim for excellence and integrity in everything we do - because lives depend on it.
  • Care: We show up for each other, our customers, and our mission - always going the extra mile.
  • Be the Change You Seek: We're adaptable, forward-thinking, and constantly improving - for the betterment of all.
  • One Team: We collaborate, support one another, and succeed together.
  • Grow for Good: We grow with purpose - to expand access to research and improve global health.
  • Own It: We take initiative, deliver results, and follow through - with passion and accountability.

Benefits
  • Comprehensive health, dental, and vision insurance
  • Enhanced EAP - mental health support
  • Flexible PTO + paid holidays
  • Continuing education reimbursement
  • 401(k) / RRSP with company match and immediate vesting

Ready to Apply?
We'd love to hear from you - apply now!
We're an equal opportunity employer committed to building a diverse and inclusive workplace. We welcome applicants from all backgrounds and will provide accommodations during the hiring process upon request.

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