The Make or Buy (MoB) Study Manager is responsible for leading the MoB function for the Industrial Strategy group. The primary responsibility is to determine new program vertical orientation ensuring ...
The Make or Buy (MoB) Study Manager is responsible for leading the MoB function for the Industrial Strategy group. The primary responsibility is to determine new program vertical orientation ensuring ...
Make or Buy Study Manager
$104K - $129K/yr
The Make or Buy (MoB) Study Manager is responsible for leading the MoB function for the Industrial Strategy group. The primary responsibility is to determine new program vertical orientation ensuring ...
Make or Buy Study Manager
$104K - $129K/yr
The Make or Buy (MoB) Study Manager is responsible for leading the MoB function for the Industrial Strategy group. The primary responsibility is to determine new program vertical orientation ensuring ...
The Sr. CSL is accountable for oversight of the contract and budget execution, study timelines, study budget management, and ensuring study conduct is in accordance with, Regeneron Standard Operating ...
The Sr. CSL is accountable for oversight of the contract and budget execution, study timelines, study budget management, and ensuring study conduct is in accordance with, Regeneron Standard Operating ...
Build Our Future Together The Manager, Precision Medicine Clinical Laboratory Study Management (CLSM Manager) will lead and develop a team of Clinical Laboratory Study managers (CLSM) for various ...
Build Our Future Together The Manager, Precision Medicine Clinical Laboratory Study Management (CLSM Manager) will lead and develop a team of Clinical Laboratory Study managers (CLSM) for various ...
This role applies to internally sourced studies and/or CRO/Partnered studies. Collaborates and interacts with clinical trial managers, development program managers, medical monitors, as well as staff ...
This role applies to internally sourced studies and/or CRO/Partnered studies. Collaborates and interacts with clinical trial managers, development program managers, medical monitors, as well as staff ...
Manager Clinical Study Lead
Warren, MI · On-site
The Manager, Clinical Study Lead may perform the following responsibilities with moderate oversight: accountable for the global execution of assigned smaller or less complex clinical trials from ...
Manager Clinical Study Lead
Warren, MI · On-site
The Manager, Clinical Study Lead may perform the following responsibilities with moderate oversight: accountable for the global execution of assigned smaller or less complex clinical trials from ...
The Manager, Clinical Study Lead may perform the following responsibilities with moderate oversight: accountable for the global execution of assigned smaller or less complex clinical trials ...
The Manager, Clinical Study Lead may perform the following responsibilities with moderate oversight: accountable for the global execution of assigned smaller or less complex clinical trials ...
Manager, Clinical Study Lead
Warren, MI · On-site
The Manager, Clinical Study Lead may perform the following responsibilities with moderate oversight: accountable for the global execution of assigned smaller or less complex clinical trials from ...
Manager, Clinical Study Lead
Warren, MI · On-site
The Manager, Clinical Study Lead may perform the following responsibilities with moderate oversight: accountable for the global execution of assigned smaller or less complex clinical trials from ...
Study Coordinator
Ann Arbor, MI · On-site
Conducting study visits and research assessments with participants (data collection using ... Familiarity with REDCap, Qualtrics, or other research management systems. * Experience coordinating ...
Study Coordinator
Ann Arbor, MI · On-site
Conducting study visits and research assessments with participants (data collection using ... Familiarity with REDCap, Qualtrics, or other research management systems. * Experience coordinating ...
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 activities as required * Supervise and maintain records of all medications
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 activities as required * Supervise and maintain records of all medications
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 activities as required * Supervise and maintain records of all medications
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 activities as required * Supervise and maintain records of all medications
We are seeking aClinical Study Associate Managerto join ourClinical Trial management team.In this role, you will support the Clinical Study Lead by taking responsibility for areas of clinical trial ...
We are seeking aClinical Study Associate Managerto join ourClinical Trial management team.In this role, you will support the Clinical Study Lead by taking responsibility for areas of clinical trial ...
We are seeking aClinical Study Associate Managerto join ourClinical Trial management team.In this role, you will support the Clinical Study Lead by taking responsibility for areas of clinical trial ...
We are seeking aClinical Study Associate Managerto join ourClinical Trial management team.In this role, you will support the Clinical Study Lead by taking responsibility for areas of clinical trial ...
We are seeking aClinical Study Associate Managerto join ourClinical Trial management team.In this role, you will support the Clinical Study Lead by taking responsibility for areas of clinical trial ...
We are seeking aClinical Study Associate Managerto join ourClinical Trial management team.In this role, you will support the Clinical Study Lead by taking responsibility for areas of clinical trial ...
Site Start up Management * Lead and oversee all aspects of site start-up activities for complex, high profile studies, including fast-track site initiation, site calls, document collection, and ...
Site Start up Management * Lead and oversee all aspects of site start-up activities for complex, high profile studies, including fast-track site initiation, site calls, document collection, and ...
We are seeking a Senior Manager, Clinical Study Inspection Readiness to join our Clinical Trial Management function, supporting inspection readiness across one or more assigned clinical programs. In ...
We are seeking a Senior Manager, Clinical Study Inspection Readiness to join our Clinical Trial Management function, supporting inspection readiness across one or more assigned clinical programs. In ...
Manage study timelines, deliverables, risks, and issue resolution * Oversee external vendors, CROs, central laboratories, imaging vendors, and specialty providers * Coordinate Clinical Trial Team ...
Manage study timelines, deliverables, risks, and issue resolution * Oversee external vendors, CROs, central laboratories, imaging vendors, and specialty providers * Coordinate Clinical Trial Team ...
Clinical Research Coord Assoc-Term Limited
Ann Arbor, MI · On-site
$23.75 - $31.50/hr
Study and Site Management * Data Management and Informatics * Leadership and Professionalism * Communication and Teamwork Essential*: 30% - Clinical Coordinator Responsibilities: Performs non-GCP ...
Clinical Research Coord Assoc-Term Limited
Ann Arbor, MI · On-site
$23.75 - $31.50/hr
Study and Site Management * Data Management and Informatics * Leadership and Professionalism * Communication and Teamwork Essential*: 30% - Clinical Coordinator Responsibilities: Performs non-GCP ...
Regional Regulation Study Lead
Auburn Hills, MI · On-site
$1.2K - $1.6K/wk
Within the PRS PPM Program Management organization is created the new Global Regulation & Transversal Studies (GRTS) Team , that operating through regional members, is the point of contact between ...
Regional Regulation Study Lead
Auburn Hills, MI · On-site
$1.2K - $1.6K/wk
Within the PRS PPM Program Management organization is created the new Global Regulation & Transversal Studies (GRTS) Team , that operating through regional members, is the point of contact between ...
Clinic Research Coordinator I
Detroit, MI · On-site
$24 - $32/hr
Liaising with Laboratory team, Data team, Administrative staff, Clinical Investigators, Research Participants and Sponsor/CRO representatives, under the direction of the Site/Study Management Team ...
Clinic Research Coordinator I
Detroit, MI · On-site
$24 - $32/hr
Liaising with Laboratory team, Data team, Administrative staff, Clinical Investigators, Research Participants and Sponsor/CRO representatives, under the direction of the Site/Study Management Team ...
Study Manager information
See Michigan salary details
$21.4K - $28.6K
9% of jobs
$28.6K - $35.9K
15% of jobs
$36.4K is the 25th percentile. Wages below this are outliers.
$35.9K - $43.1K
17% of jobs
The median wage is $45.6K / yr.
$43.1K - $50.4K
27% of jobs
$54.8K is the 75th percentile. Wages above this are outliers.
$50.4K - $57.6K
12% of jobs
$57.6K - $64.9K
8% of jobs
$64.9K - $72.1K
4% of jobs
$72.1K - $79.4K
3% of jobs
$79.4K - $86.6K
2% of jobs
$86.6K - $93.9K
2% of jobs
$93.9K - $101.1K
1% of jobs
$21.4K
$51.9K
$101.1K
How much do study manager jobs pay per year?
How does a study manager typically collaborate with cross-functional teams during the course of a clinical trial?
What are the key skills and qualifications needed to thrive as a study manager?
What does a study manager do?

Stellantis rating
7.5
Based on 130 frontline employees who took The Breakroom Quiz
14th of 44 rated automakers
Job description
Basic Qualifications:
- Bachelor's degree in engineering, finance or a relevant technical discipline.
- 5+ years of experience in Vehicle Manufacturing (stamping, welding, and assembly).
- Proven experience managing cross-functional teams and working within unionized environments.
- Strong financial acumen with experience managing complex business cases
- Excellent relationship building skills
- Excellent written and verbal communication skills, including experience interfacing with executive leadership.
- Proficiency in Microsoft Office (PowerPoint, Word, Excel).
Preferred Qualifications:
- Advanced technical or management degree
- MBA or equivalent business qualification
- 10+ years of experience in Vehicle Manufacturing (stamping, welding, and assembly)
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