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Full Time Clinical Research Rater Jobs in Michigan

Insight

Clinical Research Assistant

Flint, MI

Job Type: * Full time (on-site, in-person) * Monday to Friday, Full-time (8 hours), 8am - 5pm EST ... Clinical Research manager in executing and monitoring the overall clinical study to ensure ...

Insight

Clinical Research Assistant

Flint, MI · On-site

Job Type: * Full time (on-site, in-person) * Monday to Friday, Full-time (8 hours), 8am - 5pm EST ... Clinical Research manager in executing and monitoring the overall clinical study to ensure ...

University of Chicago Library

$60K - $75K/yr

Job Summary The CLEAR Lab is an NIH-funded research program led by clinician-scientists dedicated ... Rate Type Salary FLSA Status Exempt Pay Range $60,000.00 - $75,000.00 The included pay rate or ...

Alcanza

Clinical Research Coordinator

Farmington, MI · On-site

$23.75 - $31.75/hr

The Clinical Research Coordinator (CRC) works to ensure the execution of assigned studies in ... guidelines. * Full-time employees regularly scheduled to work at least 30 hours per week are ...

Spectrum Health

RN Clinical Research

Royal Oak, MI · On-site

The Clinical Research Nurse promotes good clinical practices in the conduct of clinical ... Full time Shift Day (United States of America) Weekly Scheduled Hours 40 Hours of Work 8-4:30 Days ...

Insight

Research Executive Assistant

Flint, MI · On-site

$18.75 - $25.75/hr

Chief Clinical Research Officer Schedule: Full-time, Monday-Friday, with flexibility for research-related deadlines Position Summary: The Research Executive Assistant provides high-level ...

New

Spectrum Health

RN Clinical Research Oncology

Grand Rapids, MI · Hybrid

$66K - $83K/yr

... research studies to enhance the advancement of clinical practice. Serves as primary coordinator ... Full time Shift Day (United States of America) Weekly Scheduled Hours 40 Hours of Work 8:30 a.m. to ...

Corewell Health

RN Clinical Research Oncology

Grand Rapids, MI · On-site

$66K - $83K/yr

... research studies to enhance the advancement of clinical practice. Serves as primary coordinator ... Full time Shift Day (United States of America) Weekly Scheduled Hours 40 Hours of Work 8:30 a.m. to ...

Tenet Health

Clinical Genetics Physician

Detroit, MI · On-site

Position Highlights * Full-time Clinical Geneticist role within the Division of Genetic, Genomic ... Flexibility to define your balance of clinical and research responsibilities * Teaching and ...

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Full Time Clinical Research Rater information

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 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 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 are the most commonly searched types of Clinical Research Rater jobs in Michigan? The most popular types of Clinical Research Rater jobs in Michigan are:
What are popular job titles related to Full Time Clinical Research Rater jobs in Michigan? For Full Time Clinical Research Rater jobs in Michigan, the most frequently searched job titles are:
What job categories do people searching Full Time Clinical Research Rater jobs in Michigan look for? The top searched job categories for Full Time Clinical Research Rater jobs in Michigan are:
What cities in Michigan are hiring for Full Time Clinical Research Rater jobs? Cities in Michigan 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 Michigan as of July 2026, with employment types broken down into 100% Full Time. Highlights an 98% In-person, and 2% Remote job distribution.
Senior Clinical Research Coordinator

Senior Clinical Research Coordinator

DM Clinical Research

Detroit, MI • On-site

$24 - $32/hr

Full-time

Posted 5 days ago

Job description

Senior Clinical Research Coordinator

Department
Clinical Operations - Detroit, MI
Employment Type
Full-Time
Minimum Experience
Experienced
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 a Senior Clinical Research Coordinator experienced in coordinating studies for one of our research sites in Detroit, MI. This position works closely with our Clinical Research staff to provide excellent care to patients participating in our clinical trials.
Responsibilities:
  • Completing DMCR-required training, including GCP and IATA.
  • Maintaining a working knowledge of current FDA regulations, GCP/ICH guidelines, organizational SOPs, guidance documents, and study protocols.
  • Adhering to their assigned protocols at their respective site(s).
  • Maintain working knowledge of current FDA GCP/ICH guidelines, organizational SOPs, guidance documents, and study protocols.
  • Collecting source and submitting source per Sponsor requirements via the Sponsor-specified CRF system.
  • Completing Sponsor-required training prior to study-start, to include, but not limited to:
a. Sponsor provided and IRB approved protocol
b. All amendments
c. Investigator Brochure
d. Sponsor-specified EDC and/or IVRS
  • Continued recruitment and screening for their assigned protocols at their respective site(s) at all times as applicable
  • Being prepared for and available at all required company meetings and monitoring visits for their assigned protocols at their respective site(s).
  • Utilizing the most recent version of the Protocol, Informed Consent, and Investigator Brochures at their respective site(s).
  • Compiling and organizing all regulatory and administrative binders for their assigned protocols at their respective site(s) upon initial receipt of and wherever applicable.
  • Creating source documents for their assigned protocols at their respective site(s).
  • Conducting patient visits, and all other protocol-required procedures and documenting these in a timely manner.
  • Reporting all Adverse and Serious Adverse Events to the appropriate authorities per Sponsor, IRB, and ICH Guidelines.
  • Completing data entry and query resolution in a timely manner.
  • Submitting required administrative paperwork per company timelines.
  • Occasionally attending out-of-town Investigator Meetings.
  • Ensuring data quality in all trials being conducted at their respective site(s).
  • Addressing and resolving all issues from that monitor letters for all assigned protocols at their respective site(s) in a timely manner.
  • Striving to meet Sponsor goals for their assigned protocols at their respective site(s).
  • Strive to ensure weekly, monthly, and quarterly assigned goals are met for their respective site(s).
  • Any other matters as assigned by management.

Requirements:
  • Have at least three (5) years of experience as a CRC, preferably with practice coordinating industry sponsored trials in a private setting.
  • Foreign Medical Graduate a plus.
  • Be an energetic, go-getter who is detail-oriented and can multi-task.
  • Be goals-driven while continuously maintaining quality.
  • Have ACRP certification, which is a plus.
  • Bilingual in Spanish is a plus.

Apply