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Full Time Clinical Research Rater Jobs in Michigan

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 ...

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 ...

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 ...

Trinity Health

Research Coordinator

Ann Arbor, MI · On-site

Employment Type: Full time Shift: Day Shift Description: Position requires working fully on-site ... Experience: * Minimum of three years of clinical research experience, with preference for ...

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 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 · On-site

Children's Hospital of Michigan is seeking a full-time Clinical Geneticist to join its Division of ... The successful candidate will have the flexibility to shape their clinical and research focus, make ...

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All JobsClinical Research Rater JobsFull Time Clinical Research Rater JobsFull Time Clinical Research Rater Jobs in Michigan

Full Time Clinical Research Rater information

Is a full time clinical research rater a good career?

A full-time clinical research rater is a role that involves evaluating clinical trial data, often requiring attention to detail and knowledge of medical terminology. It can offer stable employment and opportunities for growth in the healthcare and research industries, especially for those with relevant backgrounds or certifications. However, job satisfaction depends on individual interests and career goals in the clinical research field.

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?

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 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 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 August 2026, with employment types broken down into 100% Full Time. Highlights an 98% In-person, and 2% Remote job distribution.

Research Executive Assistant

Insight

Flint, MI • On-site

$18.75 - $25.75/hr

Full-time

Posted 13 days ago

Job description

Insight Health Systems Clinical Research
Research Executive Assistant
Title: Research Executive Assistant – Clinical Research
Location: Michigan- Flint or Dearborn (On-site required)
Reports To: Chief Clinical Research Officer
Schedule: Full-time, Monday–Friday, with flexibility for research-related deadlines
Position Summary:
The Research Executive Assistant provides high-level administrative, operational, and project
coordination support to Insight Health System’s Clinical Research leadership. This role requires hands-on
experience in clinical research/clinical Trials and a strong understanding of research workflows,
regulatory timelines, sponsor interactions, and site operations. The Research Executive Assistant
ensures seamless communication, efficient scheduling, and proactive support across a fast-paced
research environment.
Key Responsibilities:
• Manage complex calendars, meeting coordination, and travel arrangements for research leadership
• Prepare agendas, minutes, and follow-up action items for internal and external research meetings
• Draft, edit, and format correspondence, presentations, and reports related to clinical research
operations
• Maintain confidentiality and handle sensitive information with discretion
• Assist with research pipeline and study startup tasks such as feasibility coordination, document
collection, and meeting scheduling
• Support tracking of regulatory submissions, training logs, delegation logs, and study milestones
• Coordinate sponsor and CRO visits, including SIVs, IMVs, and closeout meetings
• Maintain organized filing systems for research documents, contracts, and communications
• Track deadlines, deliverables, and cross-functional tasks across multiple studies
• Support recruitment initiatives, community events, and research outreach activities
• Assist with invoice tracking, budget documentation, and vendor coordination
Minimum Qualifications:
• Minimum 2–3 years of administrative experience in clinical Trials (required)
• Strong understanding of Clinical Trials operations, regulatory processes, and sponsor interactions
• Exceptional organizational, communication, and multitasking skills
• Proficiency in Microsoft Office, CTMS platforms, and document management systems
• Ability to work independently, anticipate needs, and manage competing priorities

Apply