... feasibility, start up, regulatory, contracts and budgets, and quality functions. The Associate ... Review study protocols and develop source * Maintain ISF documentation Cross-Functional ...
... feasibility, start up, regulatory, contracts and budgets, and quality functions. The Associate ... Review study protocols and develop source * Maintain ISF documentation Cross-Functional ...
Clinical Research Coordinator Senior
Ann Arbor, MI · On-site
$23.75 - $31.50/hr
... study start-up, implementation, ongoing conduct, and close-out activities as appropriate ... Underfill Statement This position may be underfilled at the CRC-Intermediate or CRC-Associate ...
Clinical Research Coordinator Senior
Ann Arbor, MI · On-site
$23.75 - $31.50/hr
... study start-up, implementation, ongoing conduct, and close-out activities as appropriate ... Underfill Statement This position may be underfilled at the CRC-Intermediate or CRC-Associate ...
Clinical Research Coordinator Senior
Ann Arbor, MI · On-site
$23.75 - $31.50/hr
... study start-up, implementation, ongoing conduct, and close-out activities as appropriate ... Underfill Statement This position may be underfilled at the CRC-Intermediate or CRC-Associate ...
Clinical Research Coordinator Senior
Ann Arbor, MI · On-site
$23.75 - $31.50/hr
... study start-up, implementation, ongoing conduct, and close-out activities as appropriate ... Underfill Statement This position may be underfilled at the CRC-Intermediate or CRC-Associate ...
Clinical Research Coordinator Senior
Ann Arbor, MI · On-site
$23.75 - $31.50/hr
... study start-up, implementation, ongoing conduct, and close-out activities as appropriate ... Underfill Statement This position may be underfilled at the CRC-Intermediate or CRC-Associate ...
New
Clinical Research Coordinator Senior
Ann Arbor, MI · On-site
$23.75 - $31.50/hr
... study start-up, implementation, ongoing conduct, and close-out activities as appropriate ... Underfill Statement This position may be underfilled at the CRC-Intermediate or CRC-Associate ...
New
Clinical Research Coordinator A/B/C
Ann Arbor, MI · On-site
$23.75 - $31.50/hr
... study start-up activities. The CRC B will have less supervision in the management of clinical trials and will need to use more independent judgment. Clinical Research Coordinator C is expected to ...
Clinical Research Coordinator A/B/C
Ann Arbor, MI · On-site
$23.75 - $31.50/hr
... study start-up activities. The CRC B will have less supervision in the management of clinical trials and will need to use more independent judgment. Clinical Research Coordinator C is expected to ...
Clinical Research Coordinator A/B/C
Ann Arbor, MI · On-site
$23.75 - $31.50/hr
... study start-up activities. The CRC B will have less supervision in the management of clinical trials and will need to use more independent judgment. Clinical Research Coordinator C is expected to ...
Clinical Research Coordinator A/B/C
Ann Arbor, MI · On-site
$23.75 - $31.50/hr
... study start-up activities. The CRC B will have less supervision in the management of clinical trials and will need to use more independent judgment. Clinical Research Coordinator C is expected to ...
S/he will play a key role in study start-up, intake & feasibility for many studies. The Project Manager A will continue to have Research Coordinator duties as needed to meet the needs of the CTU. The ...
S/he will play a key role in study start-up, intake & feasibility for many studies. The Project Manager A will continue to have Research Coordinator duties as needed to meet the needs of the CTU. The ...
S/he will play a key role in study start-up, intake & feasibility for many studies. The Project Manager A will continue to have Research Coordinator duties as needed to meet the needs of the CTU. The ...
S/he will play a key role in study start-up, intake & feasibility for many studies. The Project Manager A will continue to have Research Coordinator duties as needed to meet the needs of the CTU. The ...
Imaging Specialist Manager
Detroit, MI · On-site +1
You will manage and coordinate the operational imaging strategy, plan, risk assessment, mitigation, and execution for oncology and non-oncology clinical trials across all phases from study start-up ...
Imaging Specialist Manager
Detroit, MI · On-site +1
You will manage and coordinate the operational imaging strategy, plan, risk assessment, mitigation, and execution for oncology and non-oncology clinical trials across all phases from study start-up ...
Registered Nurse Oncology Research Coordinator-Full Time (80 Hours per pay period) Monday-Friday 8-4
Battle Creek, MI · On-site
Participates in clinical research audits. • Maintains knowledge of current trends and developments in the research field. • Attends clinical study start-up meetings as necessary. • Demonstrates ...
Registered Nurse Oncology Research Coordinator-Full Time (80 Hours per pay period) Monday-Friday 8-4
Battle Creek, MI · On-site
Participates in clinical research audits. • Maintains knowledge of current trends and developments in the research field. • Attends clinical study start-up meetings as necessary. • Demonstrates ...
... cohort studies. The areas of application include pulmonology, diabetes, cardiovascular disease ... Generous salary and start-up support are available. The Department of Biostatistics has 43 primary ...
... cohort studies. The areas of application include pulmonology, diabetes, cardiovascular disease ... Generous salary and start-up support are available. The Department of Biostatistics has 43 primary ...
Production Associate
Howell, MI · On-site
$16 - $17/hr
Production Associate (3 shifts) Primary Job Function : Operation of the Assembly line by using the ... Perform line start up. * Load/Assemble/Weld parts. * Correct machine problems. * Inspect parts for ...
Quick apply
Production Associate
Howell, MI · On-site
$16 - $17/hr
Production Associate (3 shifts) Primary Job Function : Operation of the Assembly line by using the ... Perform line start up. * Load/Assemble/Weld parts. * Correct machine problems. * Inspect parts for ...
Unblinded Clinical Research Coordinator II
Southfield, MI · On-site
$22.25 - $29.50/hr
... aspects of company start up activities as requiredSupervise and maintain records of all ... Associates Degree required or 2 years of formal educational courseworkBachelor's degree ...
Unblinded Clinical Research Coordinator II
Southfield, MI · On-site
$22.25 - $29.50/hr
... aspects of company start up activities as requiredSupervise and maintain records of all ... Associates Degree required or 2 years of formal educational courseworkBachelor's degree ...
Research Project Mgmt II- Full Time- Day Shift (8a-4:30p)
Detroit, MI · On-site
$70K - $90K/yr
... from start-up to closeout, or ongoing research functions. Oversee day-to-day operations of team ... studies and projects. EDUCATION/EXPERIENCE REQUIRED: * Bachelor's degree in a related field and ...
Research Project Mgmt II- Full Time- Day Shift (8a-4:30p)
Detroit, MI · On-site
$70K - $90K/yr
... from start-up to closeout, or ongoing research functions. Oversee day-to-day operations of team ... studies and projects. EDUCATION/EXPERIENCE REQUIRED: * Bachelor's degree in a related field and ...
Research Project Mgmt II- Full Time- Day Shift (8a-4:30p)
Detroit, MI · On-site
$70K - $90K/yr
... from start-up to closeout, or ongoing research functions. Oversee day-to-day operations of team ... studies and projects. EDUCATION/EXPERIENCE REQUIRED: * Bachelor's degree in a related field and ...
Research Project Mgmt II- Full Time- Day Shift (8a-4:30p)
Detroit, MI · On-site
$70K - $90K/yr
... from start-up to closeout, or ongoing research functions. Oversee day-to-day operations of team ... studies and projects. EDUCATION/EXPERIENCE REQUIRED: * Bachelor's degree in a related field and ...
Unblinded Clinical Research Coordinator II (4021)
Southfield, MI · On-site
$22.25 - $29.50/hr
Study IP management ... Provide training and guidance for new team members * Assist in all aspects of company start up ...
Unblinded Clinical Research Coordinator II (4021)
Southfield, MI · On-site
$22.25 - $29.50/hr
Study IP management ... Provide training and guidance for new team members * Assist in all aspects of company start up ...
Unblinded Clinical Research Coordinator II (4021)
Southfield, MI · On-site
$22.25 - $29.50/hr
Study IP management ... Provide training and guidance for new team members * Assist in all aspects of company start up ...
Unblinded Clinical Research Coordinator II (4021)
Southfield, MI · On-site
$22.25 - $29.50/hr
Study IP management ... Provide training and guidance for new team members * Assist in all aspects of company start up ...
Unblinded Clinical Research Coordinator II (4021)
Southfield, MI · On-site
$22.25 - $29.50/hr
Study IP management ... Provide training and guidance for new team members * Assist in all aspects of company start up ...
Unblinded Clinical Research Coordinator II (4021)
Southfield, MI · On-site
$22.25 - $29.50/hr
Study IP management ... Provide training and guidance for new team members * Assist in all aspects of company start up ...
Retail Sales Associate
Wyoming, MI · On-site
$16.50/hr
A Retail Sales Associate (part-time) is a valued member of a high performing team who is empowered ... start-up. We have over 1,600 stores in 48 states across the country and are opening several new ...
Retail Sales Associate
Wyoming, MI · On-site
$16.50/hr
A Retail Sales Associate (part-time) is a valued member of a high performing team who is empowered ... start-up. We have over 1,600 stores in 48 states across the country and are opening several new ...
Retail Sales Associate
Dearborn, MI · On-site
$16.50/hr
A Retail Sales Associate (part-time) is a valued member of a high performing team who is empowered ... start-up. We have over 1,600 stores in 48 states across the country and are opening several new ...
Retail Sales Associate
Dearborn, MI · On-site
$16.50/hr
A Retail Sales Associate (part-time) is a valued member of a high performing team who is empowered ... start-up. We have over 1,600 stores in 48 states across the country and are opening several new ...
Study Start Up Associate information
See Michigan salary details
$11.10 - $14.48
3% of jobs
$14.48 - $17.85
18% of jobs
$18.51 is the 25th percentile. Wages below this are outliers.
$17.85 - $21.22
20% of jobs
The median wage is $23.27 / hr.
$21.22 - $24.59
15% of jobs
$24.59 - $27.96
11% of jobs
$27.96 - $31.33
4% of jobs
$34.20 is the 75th percentile. Wages above this are outliers.
$31.33 - $34.70
5% of jobs
$34.70 - $38.08
8% of jobs
$38.08 - $41.45
6% of jobs
$41.45 - $44.82
6% of jobs
$44.82 - $48.19
3% of jobs
$11
$27
$48
How much do study start up associate jobs pay per hour?
As of Sep 14, 2026, the average hourly pay for study start up associate in Michigan is $27.49, according to ZipRecruiter salary data. Most workers in this role earn between $18.46 and $36.25 per hour, depending on experience, location, and employer.
What is the difference between Study Start Up Associate vs Clinical Trial Coordinator?
| Aspect | Study Start Up Associate | Clinical Trial Coordinator |
|---|---|---|
| Required Credentials | Bachelor's degree, knowledge of regulatory requirements | Bachelor's degree, familiarity with clinical procedures |
| Work Environment | Regulatory and site initiation activities | Participant management and site coordination |
| Employer & Industry Usage | Pharmaceuticals, biotech, CROs | Hospitals, research centers, CROs |
The Study Start Up Associate primarily focuses on regulatory submissions, site qualification, and initiation processes, ensuring trial readiness. In contrast, the Clinical Trial Coordinator manages participant recruitment, scheduling, and data collection. Both roles are essential in clinical research but differ in their core responsibilities and focus areas.
What are popular job titles related to Study Start Up Associate jobs in Michigan?
For Study Start Up Associate jobs in Michigan, the most frequently searched job titles are:
What job categories do people searching Study Start Up Associate jobs in Michigan look for?
The top searched job categories for Study Start Up Associate jobs in Michigan are:
What cities in Michigan are hiring for Study Start Up Associate jobs?
Cities in Michigan with the most Study Start Up Associate job openings:
Associate Director Research Operations
Flint, MI • On-site
Insight
Full-time
Re-posted 22 days ago
Insight Enterprises rating
8.3
Based on 21 frontline employees who took The Breakroom Quiz
Job description
Insight Health System Clinical Research
JOB DESCRIPTION
Associate Director, Research Operations
Title: Associate Director - Research Operations
Location: Michigan
Reports To: Director of Research Operations
Schedule: Full-time, with flexibility for study visits, sponsor meetings, and operational needs
Position Summary:
The Associate Director of Research Operations is responsible for supporting Insight Health System's clinical research enterprise across multiple sites. This role is 50% focused on clinical Trials operations oversight and 50% dedicated to central feasibility, start up, regulatory, contracts and budgets, and quality functions. The Associate Director ensures operational excellence, compliance, and efficient execution of research activities across the network.
Key Responsibilities:
Clinical Operations Leadership (50%):
• Oversee day-to-day clinical research operations across assigned regions/sites
• Support site managers, team leads, coordinators, assistants, and investigators to ensure protocol adherence and visit execution
• Monitor enrollment performance, visit scheduling, and resource allocation
• Troubleshoot operational barriers and implement workflow improvements
• Support onboarding, training, and competency development for research staff
• Capability of travel between multiple locations as needed to support operational activities
Feasibility, Regulatory, Contracts, Budgets, and Quality (50%):
• Collaborate with Feasibility and start up/regulatory teams to ensure timely FQ submissions, IRB submissions, amendments, and reporting
• Support contract and budget negotiations, including feasibility review and cost analysis
• Ensure quality standards across documentation, data entry, and essential files
• Participate in internal audits, monitoring visits, and CAPA development
• Maintain alignment with SOPs, GCP, IRB and institutional requirements
Cross-Functional Collaboration:
• Serve as a liaison between research operations, regulatory, finance, legal, and executive leadership
• Support strategic planning for site growth, service expansion, and operational scaling
• Contribute to SOP development, process optimization, and system implementation
Minimum Qualifications:
• Ph.d degree in life sciences, healthcare, or related field (required)
• 5-7 years of clinical research experience, including operational leadership
• Strong knowledge of GCP, FDA regulations, IRB processes, and site management
• Experience with budgets, contracts, and regulatory and quality workflows
• Excellent communication, leadership, and problem-solving skills
JOB DESCRIPTION
Associate Director, Research Operations
Title: Associate Director - Research Operations
Location: Michigan
Reports To: Director of Research Operations
Schedule: Full-time, with flexibility for study visits, sponsor meetings, and operational needs
Position Summary:
The Associate Director of Research Operations is responsible for supporting Insight Health System's clinical research enterprise across multiple sites. This role is 50% focused on clinical Trials operations oversight and 50% dedicated to central feasibility, start up, regulatory, contracts and budgets, and quality functions. The Associate Director ensures operational excellence, compliance, and efficient execution of research activities across the network.
Key Responsibilities:
Clinical Operations Leadership (50%):
• Oversee day-to-day clinical research operations across assigned regions/sites
• Support site managers, team leads, coordinators, assistants, and investigators to ensure protocol adherence and visit execution
• Monitor enrollment performance, visit scheduling, and resource allocation
• Troubleshoot operational barriers and implement workflow improvements
• Support onboarding, training, and competency development for research staff
• Capability of travel between multiple locations as needed to support operational activities
Feasibility, Regulatory, Contracts, Budgets, and Quality (50%):
• Collaborate with Feasibility and start up/regulatory teams to ensure timely FQ submissions, IRB submissions, amendments, and reporting
• Support contract and budget negotiations, including feasibility review and cost analysis
• Ensure quality standards across documentation, data entry, and essential files
• Participate in internal audits, monitoring visits, and CAPA development
• Maintain alignment with SOPs, GCP, IRB and institutional requirements
- Review study protocols and develop source
- Maintain ISF documentation
Cross-Functional Collaboration:
• Serve as a liaison between research operations, regulatory, finance, legal, and executive leadership
• Support strategic planning for site growth, service expansion, and operational scaling
• Contribute to SOP development, process optimization, and system implementation
Minimum Qualifications:
• Ph.d degree in life sciences, healthcare, or related field (required)
• 5-7 years of clinical research experience, including operational leadership
• Strong knowledge of GCP, FDA regulations, IRB processes, and site management
• Experience with budgets, contracts, and regulatory and quality workflows
• Excellent communication, leadership, and problem-solving skills
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