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Full Time Clinical Research Rater Jobs in Ohio (NOW HIRING)

Promedica

Clinical Research Scientist

Toledo, OH · On-site

Vascular Surgery Weekly Hours: 40 Status: Full time Shift: Days (United States of America) Job Summary: As the Clinical Research Scientist, you implement investigator-initiated clinical research ...

Dayton Physicians

Clinical Research Coordinator

Kettering, OH · On-site

$21.50 - $28.75/hr

Work/life balance schedules Why work for Dayton Physician's Network? * Full-time employees are ... The clinical research coordinator (CRC) will coordinate and conduct all activities designated by ...

Care Access

Clinical Research Coordinator II

Lima, OH · On-site

$60K - $90K/yr

How This Role Makes a Difference The Clinical Research Coordinator's primary responsibilities are ... Benefits & Perks (US Full Time Employees) * Paid Time Off (PTO) and Company Paid Holidays * 100 ...

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Full Time Clinical Research Rater information

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 Ohio?

The most popular types of Clinical Research Rater jobs in Ohio are:

What are popular job titles related to Full Time Clinical Research Rater jobs in Ohio?

For Full Time Clinical Research Rater jobs in Ohio, the most frequently searched job titles are:

What job categories do people searching Full Time Clinical Research Rater jobs in Ohio look for?

The top searched job categories for Full Time Clinical Research Rater jobs in Ohio are:

What cities in Ohio are hiring for Full Time Clinical Research Rater jobs?

Cities in Ohio with the most Full Time Clinical Research Rater job openings:

Full Time Clinical Research Rater jobs near you

Clinical Research Scientist

Promedica

Toledo, OH • On-site

Full-time

Re-posted 7 days ago

ProMedica rating

6.6

Company rating: 6.6 out of 10

Based on 287 frontline employees who took The Breakroom Quiz

572nd of 898 rated healthcare providers

Job description

Location:

Toledo Hospital

Department:

Vascular Surgery

Weekly Hours:

40

Status:

Full time

Shift:

Days (United States of America)

Job Summary:

As the Clinical Research Scientist, you implement investigator-initiated clinical research studies through collaboration with physicians, researchers, and research staff.

You will develop hypotheses, research methodology, study design, statistical analysis, writing and publication of results.

The above summary is intended to describe the general nature and level of work performed by the positions. It should not be considered exhaustive.

REQUIREMENTS

  • Education: PhD Required
  • Skills: Statistical, analysis background with experience in SQL databases, experience in medical writing. Strong inter-personal skills both written and verbal required, effective verbal and written communication skills in English required. Ability to perform statistical analyses, including sample size estimation, for study design and analysis of results.
  • Years of Experience: 5 years experience in scientific research methodology and design and data analysis. Proven track record of manuscript preparation and publication. Experience working in medical/healthcare setting.

PREFERRED REQUIREMENTS

  • Education: PhD
  • Skills: Sponsored clinical trial experience desired and familiarity with clinical setting, medical terminology, and knowledge of vascular disease. Excellent computer skills including Epic EMR, Red Cap, and experience with using large datasets preferred. Healthcare experience related to cardiovascular disease processes.
  • Years of Experience: 5+ years

ProMedica is a mission-driven, not-for-profit health care organization headquartered in Toledo, Ohio. It serves communities across nine states and provides a range of services, including acute and ambulatory care, a dental plan, and academic business lines. ProMedica owns and operates 10 hospitals and has an affiliated interest in one additional hospital. The organization employs over 1,300 health care providers through ProMedica Physicians and has more than 2,300 physicians and advanced practice providers with privileges. Committed to its mission of improving health and well-being, ProMedica has received national recognition for its clinical excellence and its initiatives to address social determinants of health.For more information about ProMedica, please visitpromedica.org/aboutus.

Benefits:

We provide flexible benefits that include compensation and programs to help you take care of your family, your finances and your personal well-being. It's what makes us one of the best places to work, and helps our employees live and work to their fullest potential.

Qualified applicants will receive consideration for employment without regard to race, color, national origin, ancestry, religion, sex/gender (including pregnancy), sexual orientation, gender identity or gender expression, age, physical or mental disability, military or protected veteran status, citizenship, familial or marital status, genetics, or any other legally protected category. In compliance with the Americans with Disabilities Act Amendment Act (ADAAA), if you have a disability and would like to request an accommodation in order to apply for a job with ProMedica, please contact employment@promedica.org


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