Top 86 Background investigator Jobs in Detroit, Mi

Site Manager / Lead Clinical Research Coordinator
Confidential —Highland Park, MI
- $30 - $38 an hour
- Full-time
- Nursing
- Vital signs
- HIPAA
- Health insurance
- Dental insurance
Quick Apply
3d
Entry-Level Background and Social Media Investigator
Command Investigations, LLC —Detroit, MI
- $18 an hour
- Part-time
- Remote
- Ability to walk for extended periods
- Computer literacy
- Research
- Health insurance
- Dental insurance
Quick Apply
Field Investigator (Full-Time & Part-Time) – Detroit, MI
Origin Investigations Inc —Detroit, MI
- $20 - $30 an hour
- Part-time
- Background check
- Military
- Computer literacy
Quick Apply
14d
Research Assistant - Department of Oncology
Wayne State University —Detroit, MI
- Weekends as needed
- Background check
- English
- Office
Surveillance Investigator
Frasco Inc —Detroit, MI
- $20 - $26 an hour
- Weekends as needed
- Clean driving record
- Military
- Writing skills
- Paid training
- Mileage reimbursement
Research Assistant, Population Sciences - Department of Oncology
Wayne State University —Detroit, MI
- Weekends as needed
- Background check
- Nursing
- Microsoft Excel
Desktop Investigator - Canvassing - Part Time
Command Investigations, LLC —Detroit, MI
- $18 an hour
- Part-time
- Remote
- Customer service
- Ability to walk for extended periods
- Computer literacy
- 401(k)
- Referral program
Quick Apply
10d
Research Assistant - Department of Internal Medicine
Wayne State University —Detroit, MI
- Weekends as needed
- Background check
- Internal Medicine
- Office
Manager, Research Administration - Department of Internal Medicine
Wayne State University —Detroit, MI
- Full-time
- Background check
- 7 years
- Inventory management
Clinical Research Coordinator
EmVenio Research —Garden City, MI
- $56,160 - $76,960 a year
- Full-time
- Microsoft Word
- Bachelor of Science
- Mid-level
- Health savings account
- Disability insurance
Quick Apply
Project Assistant - Department of Emergency Medicine
Wayne State University —Detroit, MI
- Full-time
- Background check
- Management
- Mid-level
Special Investigations Unit (SIU) - Field Investigator
Ethos Risk Services —Detroit, MI
- $25 - $30 an hour
- Part-time
- Military
- Mid-level
- Residential
- Paid time off
- Referral program
Quick Apply
Research Assistant - Department of Pediatrics
Wayne State University —Detroit, MI
- $15 - $25 an hour
- Part-time
- Background check
- Bachelor of Science
- Office
Instructional Technology Designer - College of Nursing
Wayne State University —Detroit, MI
- $56,131 - $67,354 a year
- Full-time
- Background check
- Computer Science
- Word processing
11d
Research Associate - Department of Physiology
Wayne State University —Detroit, MI
- Weekends as needed
- Background check
- Mid-level
- Office
Research Assistant - Department of Neurology
Wayne State University —Detroit, MI
- Weekends as needed
- Background check
- Mid-level
- Office
Research Associate - Department of Oncology
Wayne State University —Detroit, MI
- Weekends as needed
- Background check
- Mid-level
- Office
Experienced Insurance Claims Surveillance Investigator
Advantage Investigations —Sterling Heights, MI
- $20 - $30 an hour
- Part-time
- Background check
- Clean driving record
- Military
- Travel reimbursement
- Paid time off
Quick Apply
7d
Program/Project Assistant II - Department of Pharmacology
Wayne State University —Detroit, MI
- $48,228 - $57,868 a year
- Full-time
- Background check
- Mid-level
- Analysis skills
International Medical Graduate (IMG) - Clinical Research
Revival Research Institute, LLC —Southfield, MI
- Full-time
- Medicine
- Microsoft Excel
- Microsoft Outlook
Quick Apply

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Site Manager / Lead Clinical Research Coordinator

Confidential
Highland Park, MI

Quick Apply

Job Details

Full-time
$30 - $38 an hour
3 days ago

Benefits

Health insurance
Dental insurance
401(k)
Vision insurance
Life insurance

Qualifications

Statistical software
Statistics
Staff supervision
Teamwork
Vital signs
Electronic health records (EHR) management
Research ethical considerations
Project documentation
Team leadership
Safety regulations
Professional ethics
HIPAA
Phlebotomy specimen handling
Clinical audit and monitoring
Clinical laboratory experience
Data integrity and documentation
ICH guidelines
Records management
Attention to detail
Data quality monitoring
Project management experience in healthcare
CDISC standards
Managing clinical research teams
Health information regulatory compliance
Organizational skills
Leading team collaboration initiatives
Research regulatory compliance
Health information management
Productivity software
Managing patient records

Full Job Description

Job Overview

MUST HAVE PHLEBOTOMY EXPERIENCE

We are seeking a dynamic and highly organized Site Manager / Lead Clinical Research Coordinator to oversee the planning, execution, and management of clinical trials at our Detroit, Michigan research site.

This pivotal role involves leading a team of research professionals, ensuring compliance with regulatory standards, and maintaining the highest standards of data quality and patient care. The ideal candidate will possess strong leadership abilities, extensive clinical research experience, and a passion for advancing healthcare through meticulous project management.

Join our Detroit team and make a meaningful impact on medical innovation while fostering a collaborative, compliant, and patient-centered research environment.

Responsibilities

Lead and supervise the clinical research team, including clinical research coordinators, nurses, and support staff, to ensure efficient daily site and trial operations.
Oversee patient recruitment, screening, informed consent, enrollment, and ongoing monitoring to ensure participant safety and adherence to study protocols.
Manage study documentation, source document review, data collection, and data management in accordance with Good Clinical Practice guidelines and applicable regulatory requirements.
Ensure compliance with FDA regulations, ICH GCP standards, HIPAA privacy requirements, institutional policies, and study-specific procedures.
Coordinate with sponsors, contract research organizations, regulatory bodies, investigators, and internal teams to support study start-up, monitoring visits, audits, inspections, and closeout activities.
Maintain complete and accurate trial records using electronic medical record systems, clinical trial management systems, electronic data capture platforms, and other data-management tools.
Review source documents and study data for accuracy, completeness, consistency, and timely entry.
Conduct regular staff training on clinical trial protocols, ethical guidelines, safety procedures, blood sampling, vital-sign measurement, and documentation standards.
Monitor staff performance, delegate responsibilities, and provide ongoing coaching and operational support.
Support quality-assurance activities and implement corrective and preventive actions when necessary.
Maintain site readiness for sponsor monitoring visits, audits, and regulatory inspections.

Requirements

At least two years of clinical research experience.
At least two years of phlebotomy experience.
At least one year of mental health research experience.
Previous supervisory or leadership experience in a clinical research or healthcare environment.
Strong knowledge of medical terminology, clinical laboratory procedures, blood-sampling techniques, phlebotomy, and vital-sign assessment.
Thorough understanding of FDA regulations, ICH GCP guidelines, CDISC data standards, HIPAA requirements, and healthcare compliance practices.
Current Good Clinical Practice certification.
Experience with clinical trial management systems, electronic medical record systems, electronic data capture platforms, statistical or data-analysis software, and Microsoft Office.
Demonstrated ability to review complex study documentation accurately while maintaining exceptional attention to detail.
Excellent project-management and organizational skills, with experience coordinating research projects from study start-up through closeout.
Knowledge of clinical research ethics, participant protection requirements, and quality-assurance standards.
Strong written and verbal communication skills.
Ability to manage competing priorities, meet deadlines, and work effectively with sponsors, investigators, staff, and study participants.
A nursing or healthcare-related background is preferred.
Clinical laboratory experience is highly desirable.

Benefits

401(k)
Dental insurance
Health insurance
Retirement plan
Vision insurance

Experience

Clinical research: 2 years required
Phlebotomy: 2 years required
Mental health research: 1 year required

Location

Detroit, MI — required
Work Location: In person at our Detroit research site

Join us in advancing groundbreaking medical research and leading projects that improve lives. We are committed to creating an inclusive workplace where your expertise can thrive while making a tangible difference in healthcare innovation. This is a paid position with opportunities for continued professional growth within a vibrant research community.

Pay: $30.00 - $38.00 per hour

Benefits:

401(k)
Dental insurance
Health insurance
Life insurance
Vision insurance

Work Location: In person

Quick Apply

Refine Your Search

background investigator jobs in detroit, mi

Site Manager / Lead Clinical Research Coordinator

Entry-Level Background and Social Media Investigator

Field Investigator (Full-Time & Part-Time) – Detroit, MI

Research Assistant - Department of Oncology

Surveillance Investigator

Research Assistant, Population Sciences - Department of Oncology

Desktop Investigator - Canvassing - Part Time

Research Assistant - Department of Internal Medicine

Manager, Research Administration - Department of Internal Medicine

Clinical Research Coordinator

Project Assistant - Department of Emergency Medicine

Special Investigations Unit (SIU) - Field Investigator

Research Assistant - Department of Pediatrics

Instructional Technology Designer - College of Nursing

Research Associate - Department of Physiology

Research Assistant - Department of Neurology

Research Associate - Department of Oncology

Experienced Insurance Claims Surveillance Investigator

Program/Project Assistant II - Department of Pharmacology

International Medical Graduate (IMG) - Clinical Research

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