Cleveland, OH · Remote
$60 - $80/hr
The ideal candidate brings 8-10 years of clinical operations experience (including 4-5+ years in study management within pharma/biotech) and is comfortable managing timelines, budgets, vendors, and ...
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Cleveland, OH · Remote
$60 - $80/hr
The ideal candidate brings 8-10 years of clinical operations experience (including 4-5+ years in study management within pharma/biotech) and is comfortable managing timelines, budgets, vendors, and ...
Cleveland, OH · Remote
$60 - $80/hr
The ideal candidate brings 8-10 years of clinical operations experience (including 4-5+ years in study management within pharma/biotech) and is comfortable managing timelines, budgets, vendors, and ...
Quick apply
Cleveland, OH · Remote
$60 - $80/hr
The ideal candidate brings 8-10 years of clinical operations experience (including 4-5+ years in study management within pharma/biotech) and is comfortable managing timelines, budgets, vendors, and ...
Durham, NC · On-site
Primary Responsibilities " Provide day-to-day study management support and oversight for assigned clinical study activities from start-up through close-out. " Coordinate with internal project team ...
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Durham, NC · On-site
Primary Responsibilities " Provide day-to-day study management support and oversight for assigned clinical study activities from start-up through close-out. " Coordinate with internal project team ...
The Clinical Study Manager must be able to work independently on multiple complex clinical studies ... Collaborate with data management team and/or CRO to ensure appropriate data capture, query ...
The Clinical Study Manager must be able to work independently on multiple complex clinical studies ... Collaborate with data management team and/or CRO to ensure appropriate data capture, query ...
Sunnyvale, CA · On-site +1
The candidate will be required to work closely with clinical research associates (CRAs), clinical trial assistants (CTAs) and data management for the conduct and execution of the study, as well as ...
Sunnyvale, CA · On-site +1
The candidate will be required to work closely with clinical research associates (CRAs), clinical trial assistants (CTAs) and data management for the conduct and execution of the study, as well as ...
The candidate will be required to work closely with clinical research associates (CRAs), clinical trial assistants (CTAs) and data management for the conduct and execution of the study, as well as ...
The candidate will be required to work closely with clinical research associates (CRAs), clinical trial assistants (CTAs) and data management for the conduct and execution of the study, as well as ...
Sunnyvale, CA · On-site +1
The candidate will be required to work closely with clinical research associates (CRAs), clinical trial assistants (CTAs) and data management for the conduct and execution of the study, as well as ...
Sunnyvale, CA · On-site +1
The candidate will be required to work closely with clinical research associates (CRAs), clinical trial assistants (CTAs) and data management for the conduct and execution of the study, as well as ...
Global Study Associate Director Location: Durham, NC Introduction to role: Are you ready to lead ... Clinical Program Team Issue Management and CAPA: Identify, report, and resolve quality issues ...
Global Study Associate Director Location: Durham, NC Introduction to role: Are you ready to lead ... Clinical Program Team Issue Management and CAPA: Identify, report, and resolve quality issues ...
Oversee contract research organizations (CROs), clinical research associates (CRAs), and third ... Oversee site management activities, including site start-up, monitoring, and close-out, to ensure ...
Quick apply
Oversee contract research organizations (CROs), clinical research associates (CRAs), and third ... Oversee site management activities, including site start-up, monitoring, and close-out, to ensure ...
Global Study Associate Director Location: Durham, NC Introduction to role: Are you ready to lead ... Proven project management experience on a global level * Experience in all phases of a clinical ...
Global Study Associate Director Location: Durham, NC Introduction to role: Are you ready to lead ... Proven project management experience on a global level * Experience in all phases of a clinical ...
Global Study Associate Director Location: Durham, NC Introduction to role: Are you ready to lead ... Proven project management experience on a global level * Experience in all phases of a clinical ...
Global Study Associate Director Location: Durham, NC Introduction to role: Are you ready to lead ... Proven project management experience on a global level * Experience in all phases of a clinical ...
Global Study Associate Director Location: Durham, NC Introduction to role: Are you ready to lead ... Proven project management experience on a global level * Experience in all phases of a clinical ...
Global Study Associate Director Location: Durham, NC Introduction to role: Are you ready to lead ... Proven project management experience on a global level * Experience in all phases of a clinical ...
Global Study Associate Director Location: Durham, NC Introduction to role: Are you ready to lead ... Proven project management experience on a global level * Experience in all phases of a clinical ...
Global Study Associate Director Location: Durham, NC Introduction to role: Are you ready to lead ... Proven project management experience on a global level * Experience in all phases of a clinical ...
Global Study Associate Director Location: Durham, NC Introduction to role: Are you ready to lead ... Proven project management experience on a global level * Experience in all phases of a clinical ...
Global Study Associate Director Location: Durham, NC Introduction to role: Are you ready to lead ... Proven project management experience on a global level * Experience in all phases of a clinical ...
Sunnyvale, CA · On-site +1
The candidate will be required to work closely with clinical research associates (CRAs), clinical trial assistants (CTAs) and data management for the conduct and execution of the study, as well as ...
Sunnyvale, CA · On-site +1
The candidate will be required to work closely with clinical research associates (CRAs), clinical trial assistants (CTAs) and data management for the conduct and execution of the study, as well as ...
Sunnyvale, CA · On-site +1
The candidate will be required to work closely with clinical research associates (CRAs), clinical trial assistants (CTAs) and data management for the conduct and execution of the study, as well as ...
Sunnyvale, CA · On-site +1
The candidate will be required to work closely with clinical research associates (CRAs), clinical trial assistants (CTAs) and data management for the conduct and execution of the study, as well as ...
Sunnyvale, CA · On-site +1
The candidate will be required to work closely with clinical research associates (CRAs), clinical trial assistants (CTAs) and data management for the conduct and execution of the study, as well as ...
Sunnyvale, CA · On-site +1
The candidate will be required to work closely with clinical research associates (CRAs), clinical trial assistants (CTAs) and data management for the conduct and execution of the study, as well as ...
Naples, FL · On-site
Collaborate with Data Management team to ensure the electronic data capture system (EDC) is ... Prepare and track clinical study budgets that include both sponsor costs and sites costs.
Naples, FL · On-site
Collaborate with Data Management team to ensure the electronic data capture system (EDC) is ... Prepare and track clinical study budgets that include both sponsor costs and sites costs.
Minneapolis, MN · On-site
$140K - $180K/yr
The Clinical Study Manager must be able to work independently on multiple complex clinical studies ... Collaborate with data management team and/or CRO to ensure appropriate data capture, query ...
Minneapolis, MN · On-site
$140K - $180K/yr
The Clinical Study Manager must be able to work independently on multiple complex clinical studies ... Collaborate with data management team and/or CRO to ensure appropriate data capture, query ...
Naples, FL · On-site
Collaborate with Data Management team to ensure the electronic data capture system (EDC) is ... Prepare and track clinical study budgets that include both sponsor costs and sites costs.
Naples, FL · On-site
Collaborate with Data Management team to ensure the electronic data capture system (EDC) is ... Prepare and track clinical study budgets that include both sponsor costs and sites costs.
$12.74 - $16.61
3% of jobs
$16.61 - $20.48
18% of jobs
$21.24 is the 25th percentile. Wages below this are outliers.
$20.48 - $24.34
20% of jobs
The median wage is $26.69 / hr.
$24.34 - $28.21
15% of jobs
$28.21 - $32.08
11% of jobs
$32.08 - $35.95
4% of jobs
$39.24 is the 75th percentile. Wages above this are outliers.
$35.95 - $39.82
5% of jobs
$39.82 - $43.68
8% of jobs
$43.68 - $47.55
6% of jobs
$47.55 - $51.42
6% of jobs
$51.42 - $55.29
3% of jobs
$12
$31
$55
For Clinical Study Management Associate jobs, the most frequently searched job titles are:
Cleveland, OH • Remote
$60 - $80/hr
Contractor
Medical, Dental, Vision, Life, Retirement
Re-posted 15 days ago
Job Title: Senior Clinical Study Manager (CSM) Location: 100% Remote Type: Contract - 6 months with desire to go permanent Compensation: $60.00 - $80.00 Work Model: Remote – offsite
Joule is current looking to hire aSenior Clinical Study Manager (CSM) to support clinical programs focused on cell/gene therapy and oncology for one of our clients. This is a remote, 40-hour/week contract (initial ~6 months) with the potential to renew or convert to full-time based on project need, performance, and budget. In this role, you will lead day-to-day study execution by partnering with CROs, sites, and cross-functional stakeholders while ensuring compliance with ICH-GCP and FDA requirements. The ideal candidate brings 8–10 years of clinical operations experience (including 4–5+ years in study management within pharma/biotech) and is comfortable managing timelines, budgets, vendors, and TMF oversight in a fast-paced environment.
Responsibilities
Requirements
System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.
System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.
#LI-EL1 Ref: #568-Clinical
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System One helps employers get work done more efficiently and economically without compromising quality. Over our 35+ year history, we've helped connect thousands of talented people with innovative companies. The excitement of a perfect fit motivates us every single day.
Business consulting services and recruiting and staffing services
5,001 - 10,000 Employees
Pittsburgh, PA, US
