Top 3 Phlebotomy supervisor Jobs in Taylor Mi

Site Manager / Lead Clinical Research Coordinator
Confidential —Highland Park, MI
- $30 - $38 an hour
- Full-time
- Background check
- Nursing
- Vital signs
- Health insurance
- Dental insurance
Quick Apply
8d
Blood Collections Supervisor
American Red Cross —Novi, MI
- From $60,000 a year
- Weekends as needed
- Clean driving record
- Computer literacy
- Mid-level
- Paid training
- Paid holidays
Supervisor - Ambulatory Laboratory Services
Henry Ford Health —Dearborn, MI
- Day shift
- Hospital
- 5 years
- Word processing
- Health insurance
- Dental insurance

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Blood Collections Supervisor
American Red Cross —Novi, MI
A current, valid driver's license with a good driving record is required . Bachelor’s degree OR a combination of education and work experience (four to eight…
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Medical Screener - Reception Technician (Customer Service)
CSL Plasma —Lincoln Park, MI
The screening procedures includes but are not limited to: assessing the self-administered health history, answering basic medical questions associated with the…
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Remains current in the field. ASCP or equivalent certification required within two years of hire. 30% Supervises and directs department technical operations and…
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Acts as interdepartmental liaison resolving operational and technical problems within department and between laboratory and other departments as they arise.

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Site Manager / Lead Clinical Research Coordinator

Confidential
Highland Park, MI

Quick Apply

Job Details

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

Benefits

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

Qualifications

Statistical software
Statistics
Staff supervision
Teamwork
Vital signs
Operations management
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

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

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phlebotomy supervisor jobs in taylor mi

Site Manager / Lead Clinical Research Coordinator

Blood Collections Supervisor

Supervisor - Ambulatory Laboratory Services

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