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Full Time Clinical Research Rater Jobs in Detroit, MI

Actalent

Clinical Research Coordinator

Detroit, MI · Hybrid

$27 - $35/hr

Clinical research certification or willingness to obtain certification Schedule & Work Environment * Full-time, 8-hour shifts * Start times between 7:00 AM and 9:00 AM based on patient schedules

Actalent

Clinical Research Coordinator

Detroit, MI · Hybrid

$27 - $35/hr

Clinical research certification or willingness to obtain certification Schedule & Work Environment * Full-time, 8-hour shifts * Start times between 7:00 AM and 9:00 AM based on patient schedules

Spectrum Health

Research Scientist

Royal Oak, MI

Royal Oak Urology Research - Full time, day shift About Corewell Health William Beaumont University ... Corewell is the exclusive clinical partner of the Oakland University William Beaumont School of ...

Corewell Health

Research Scientist

Royal Oak, MI · On-site

Royal Oak Urology Research - Full time, day shift About Corewell Health William Beaumont University ... Corewell is the exclusive clinical partner of the Oakland University William Beaumont School of ...

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 ...

Tenet Health

Clinical Geneticist

Detroit, MI

Children's Hospital of Michigan is seeking a full-time Clinical Geneticist to join its Division of ... The role offers flexibility to shape clinical and research focus, step into leadership, and make a ...

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Full Time Clinical Research Rater information

See Detroit, MI salary details

$8

$22

$45

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

As of Sep 5, 2026, the average hourly pay for full time clinical research rater in Detroit, MI is $22.48, according to ZipRecruiter salary data. Most workers in this role earn between $17.12 and $25.72 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 Detroit, MI?

The most popular types of Clinical Research Rater jobs in Detroit, MI are:

What are popular job titles related to Full Time Clinical Research Rater jobs in Detroit, MI?

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

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

The top searched job categories for Full Time Clinical Research Rater jobs in Detroit, MI are:

What cities near Detroit, MI are hiring for Full Time Clinical Research Rater jobs?

Cities near Detroit, MI 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 Detroit, MI as of August 2026, with employment types broken down into 100% Full Time. Highlights an 95% In-person, and 5% Remote job distribution, with an average salary of $46,766 per year, or $22.5 per hour.

Senior Clinical Research Coordinator

DM Clinical Research

Detroit, MI • On-site

$24 - $32/hr

Full-time

Re-posted 16 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