Clinical Research Coordinator 2 - Study Start Up (Hybrid Opportunity)
Palo Alto, CA · On-site
$28.50 - $38/hr
... studies ... Specific activities include managing start-up across various clinical trials at a time; helping ...
Clinical Research Coordinator 2 - Study Start Up (Hybrid Opportunity)
Palo Alto, CA · On-site
$28.50 - $38/hr
... studies ... Specific activities include managing start-up across various clinical trials at a time; helping ...
Generates, manages, and maintains high quality study start up and recruitment timelines for region and tracks progress towards these * Ensures that the clinical study is operationally feasible in the ...
Generates, manages, and maintains high quality study start up and recruitment timelines for region and tracks progress towards these * Ensures that the clinical study is operationally feasible in the ...
Study Start-Up Project Manager
Irving, TX · On-site +1
Our clinical operations activities are growing rapidly, and we are currently seeking a full-time Study Start-Up Project Manager to join our Site Activation and Maintenance team. This position plays a ...
Study Start-Up Project Manager
Irving, TX · On-site +1
Our clinical operations activities are growing rapidly, and we are currently seeking a full-time Study Start-Up Project Manager to join our Site Activation and Maintenance team. This position plays a ...
Study Start-Up Specialist
Chicago, IL · On-site
$55K - $70K/yr
Deep understanding of study start-up and site activation. * Knowledge of current FDA regulations ... clinical research, and HIPAA compliance. * Strong project management skills, with the ability to ...
Study Start-Up Specialist
Chicago, IL · On-site
$55K - $70K/yr
Deep understanding of study start-up and site activation. * Knowledge of current FDA regulations ... clinical research, and HIPAA compliance. * Strong project management skills, with the ability to ...
Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, Study Start-Up Project Manager to join our Site Activation and Maintenance team. This position plays ...
Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, Study Start-Up Project Manager to join our Site Activation and Maintenance team. This position plays ...
Study Start-Up Project Manager
Irving, TX · On-site
Our clinical operations activities are growing rapidly, and we are currently seeking a full-time Study Start-Up Project Manager to join our Site Activation and Maintenance team. This position plays a ...
Study Start-Up Project Manager
Irving, TX · On-site
Our clinical operations activities are growing rapidly, and we are currently seeking a full-time Study Start-Up Project Manager to join our Site Activation and Maintenance team. This position plays a ...
Primary Function of the Position This position requires a candidate with extensive experience with planning, study start-up, and execution of clinical studies. This Lead Clinical Study Manager-4 (CSM ...
Primary Function of the Position This position requires a candidate with extensive experience with planning, study start-up, and execution of clinical studies. This Lead Clinical Study Manager-4 (CSM ...
Study Start-Up Project Manager
Cincinnati, OH · On-site +1
Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, Study Start-Up Project Manager to join our Site Activation and Maintenance team. This position plays ...
Study Start-Up Project Manager
Cincinnati, OH · On-site +1
Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, Study Start-Up Project Manager to join our Site Activation and Maintenance team. This position plays ...
This position works both independently and collaboratively with a team to meet common goals and plays a key role in the clinical trial management and study start-up process at Medpace. We have ...
This position works both independently and collaboratively with a team to meet common goals and plays a key role in the clinical trial management and study start-up process at Medpace. We have ...
Experienced Study Start-Up Coordinator
Cincinnati, OH · On-site +1
This position works both independently and collaboratively with a team to meet common goals and plays a key role in the clinical trial management and study start-up process at Medpace. We have ...
Experienced Study Start-Up Coordinator
Cincinnati, OH · On-site +1
This position works both independently and collaboratively with a team to meet common goals and plays a key role in the clinical trial management and study start-up process at Medpace. We have ...
Clinical Research Regulatory & Study Start-Up Coordinator
Nashville, TN · On-site
$23.50 - $31.25/hr
Manage Others No Description POSITION SUMMARY Urology Associates, P.C. is seeking a detail-oriented and regulatory-minded Clinical Research Regulatory & Study Start-Up Coordinator to join our growing ...
Clinical Research Regulatory & Study Start-Up Coordinator
Nashville, TN · On-site
$23.50 - $31.25/hr
Manage Others No Description POSITION SUMMARY Urology Associates, P.C. is seeking a detail-oriented and regulatory-minded Clinical Research Regulatory & Study Start-Up Coordinator to join our growing ...
In this position you will work independently and collaboratively to manage timelines, meet goals, and play a key role in the clinical trial management and study start-up process at Medpace. If you ...
In this position you will work independently and collaboratively to manage timelines, meet goals, and play a key role in the clinical trial management and study start-up process at Medpace. If you ...
Study Start-Up Associate II
Rockville, MD · On-site
$34.25 - $46.75/hr
Overview Study Start-Up Associate II US Remote Emmes Group: Building a better future for us all ... Ability to manage multiple competing priorities within various clinical trials. * Ability to work ...
Study Start-Up Associate II
Rockville, MD · On-site
$34.25 - $46.75/hr
Overview Study Start-Up Associate II US Remote Emmes Group: Building a better future for us all ... Ability to manage multiple competing priorities within various clinical trials. * Ability to work ...
This position works both independently and collaboratively with a team to meet common goals and plays a key role in the clinical trial management and study start-up process at Medpace. We are seeking ...
This position works both independently and collaboratively with a team to meet common goals and plays a key role in the clinical trial management and study start-up process at Medpace. We are seeking ...
Director, Study Start-Up
$195K - $275K/yr
Provide strategic and operational leadership for endtoend study startup activities across assigned ... Strong understanding of clinical trial management, ICH-GCP, and regulatory compliance * Proven ...
Director, Study Start-Up
$195K - $275K/yr
Provide strategic and operational leadership for endtoend study startup activities across assigned ... Strong understanding of clinical trial management, ICH-GCP, and regulatory compliance * Proven ...
Sr. Clinical Study Manager
Naples, FL · On-site
Requisition ID: 66722 Title: Sr. Clinical Study Manager Arthrex, Inc. is a global medical device ... Manages site initiation activities (e.g., study start-up documentation preparation) * Responsible ...
Sr. Clinical Study Manager
Naples, FL · On-site
Requisition ID: 66722 Title: Sr. Clinical Study Manager Arthrex, Inc. is a global medical device ... Manages site initiation activities (e.g., study start-up documentation preparation) * Responsible ...
This position works both independently and collaboratively with a team to meet common goals and plays a key role in the clinical trial management and study start-up process at Medpace. If you want to ...
This position works both independently and collaboratively with a team to meet common goals and plays a key role in the clinical trial management and study start-up process at Medpace. If you want to ...
Study Start Up Associate II
Pittsburgh, PA · On-site
$32.50 - $44.50/hr
Study Start-Up Specialist (Sponsor Dedicated) ICON is a global healthcare intelligence and clinical ... Requires proven project management skills * Must have excellent interpersonal, written and verbal ...
Study Start Up Associate II
Pittsburgh, PA · On-site
$32.50 - $44.50/hr
Study Start-Up Specialist (Sponsor Dedicated) ICON is a global healthcare intelligence and clinical ... Requires proven project management skills * Must have excellent interpersonal, written and verbal ...
Study Activation Manager
Raleigh, NC · On-site
Proficiency with clinical trial management systems, start-up tracking tools, and standard business ... in study start-up, site activation, clinical operations, or clinical trial management. About CTI ...
Study Activation Manager
Raleigh, NC · On-site
Proficiency with clinical trial management systems, start-up tracking tools, and standard business ... in study start-up, site activation, clinical operations, or clinical trial management. About CTI ...
Clinical Trial Associate II
Cambridge, MA · On-site
$75K - $90K/yr
With minimal oversight, manage all study start up, maintenance and closeout site management responsibilities, under the supervision of the Clinical Trial Manager * Lead the maintenance of audit-ready ...
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Clinical Trial Associate II
Cambridge, MA · On-site
$75K - $90K/yr
With minimal oversight, manage all study start up, maintenance and closeout site management responsibilities, under the supervision of the Clinical Trial Manager * Lead the maintenance of audit-ready ...
Clinical Study Start Up Manager information
See salary details
$22K - $38.7K
1% of jobs
$38.7K - $55.5K
3% of jobs
$55.5K - $72.2K
7% of jobs
$87.1K is the 25th percentile. Wages below this are outliers.
$72.2K - $88.9K
15% of jobs
$88.9K - $105.6K
9% of jobs
$105.6K - $122.4K
14% of jobs
The median wage is $123.4K / yr.
$122.4K - $139.1K
17% of jobs
$150.9K is the 75th percentile. Wages above this are outliers.
$139.1K - $155.8K
13% of jobs
$155.8K - $172.5K
11% of jobs
$172.5K - $189.3K
7% of jobs
$189.3K - $206K
3% of jobs
$22K
$125.3K
$206K
How much do clinical study start up manager jobs pay per year?
As of Sep 11, 2026, the average yearly pay for clinical study start up manager in the United States is $125,290.00, according to ZipRecruiter salary data. Most workers in this role earn between $85,000.00 and $157,000.00 per year, depending on experience, location, and employer.
What are the most commonly searched types of Clinical Study Start Up jobs?
The most popular types of Clinical Study Start Up jobs are:
What are popular job titles related to Clinical Study Start Up Manager jobs?
For Clinical Study Start Up Manager jobs, the most frequently searched job titles are:
Clinical Research Coordinator 2 - Study Start Up (Hybrid Opportunity)
Palo Alto, CA • On-site
Stanfordlivetickets
$28.50 - $38/hr
Other
Posted 9 days ago
Job description
The Department of Medicine (DoM) Clinical Research Hub (CRH) at Stanford University is seeking a Clinical Research Coordinator 2 in Study Start Up Group to perform duties related to the coordination of clinical studies in support of multiple therapeutic disciplines to bring together the expertise of professionals from different fields to address scientific challenges. This collaborative effort allows the Department of Medicine to make meaningful medical advancements by translating research discoveries into clinical practice to improve health worldwide.
This role will support study start up activities for interventional and observational clinical research trials and studies. Specific activities include managing start-up across various clinical trials at a time; helping with start-up processes; providing status reports, metrics and forecasts to CRM and collaborators; assisting with development of effective budgets and plan for resources; and ensuring all studies receive appropriate regulatory approvals for compliance and quality downstream during study execution. This is a hybrid role, with ability to coordinate moderately complex aspects of one or more clinical studies, ability to task switch in a high-energy environment, outstanding communication and organizational skills, ability to work independently, ability to proactively manage challenges in clinical research and attention to detail are required in a successful candidate. The CRC2 will present updates at study meetings and huddles, and be responsible for ensuring compliance with federal, state, local, institutional and sponsor regulations; and work under close direction of the principal investigator and/or study coordinator/supervisor. Other duties may also be assigned.