Collaborate with Clinical Research Associates (CRAs) and the local study team to meet start-up milestones. * Participate in Local Study Team meetings and report on site performance metrics. * Ensure ...
Collaborate with Clinical Research Associates (CRAs) and the local study team to meet start-up milestones. * Participate in Local Study Team meetings and report on site performance metrics. * Ensure ...
Study Start Up Coordinator
New Orleans, LA · On-site
$50K/yr
The Study Start Up Coordinator Coordinator is a strategic project management role, ensuring a successful start to clinical research trials across our site network. This position is ideal for someone ...
Study Start Up Coordinator
New Orleans, LA · On-site
$50K/yr
The Study Start Up Coordinator Coordinator is a strategic project management role, ensuring a successful start to clinical research trials across our site network. This position is ideal for someone ...
Study Start Up Coordinator
New Orleans, LA · On-site
Study Start Up Coordinator's Main Objective Overall, the Study Start Up Coordinator is responsible for supporting efficient, accurate, and organized study start-up operations for clinical trials ...
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Study Start Up Coordinator
New Orleans, LA · On-site
Study Start Up Coordinator's Main Objective Overall, the Study Start Up Coordinator is responsible for supporting efficient, accurate, and organized study start-up operations for clinical trials ...
Study Start Up Manager
Wilmington, DE · Hybrid
Study Start Up Manager - Hybrid Role On-Site Are you ready to take on a pivotal role in the Site Activation Team as a Study Start Up Manager. As a key player in the US study team, you'll be ...
Study Start Up Manager
Wilmington, DE · Hybrid
Study Start Up Manager - Hybrid Role On-Site Are you ready to take on a pivotal role in the Site Activation Team as a Study Start Up Manager. As a key player in the US study team, you'll be ...
Study Start Up Manager
Wilmington, DE · On-site
Study Start Up Manager - Hybrid Role On-Site Are you ready to take on a pivotal role in the Site Activation Team as a Study Start Up Manager? As a key player in the US study team, you'll be ...
Study Start Up Manager
Wilmington, DE · On-site
Study Start Up Manager - Hybrid Role On-Site Are you ready to take on a pivotal role in the Site Activation Team as a Study Start Up Manager? As a key player in the US study team, you'll be ...
Director, Study Start-Up
Watertown, MA · On-site
$195K - $275K/yr
Provide strategic and operational leadership for end-to-end study start-up activities across assigned clinical programs, ensuring timely, compliant, and high-quality site activation. * Accountable ...
Director, Study Start-Up
Watertown, MA · On-site
$195K - $275K/yr
Provide strategic and operational leadership for end-to-end study start-up activities across assigned clinical programs, ensuring timely, compliant, and high-quality site activation. * Accountable ...
Study Start Up Manager
Wilmington, DE · On-site
Study Start Up Manager - Hybrid Role On-Site Are you ready to take on a pivotal role in the Site Activation Team as a Study Start Up Manager? As a key player in the US study team, you'll be ...
Study Start Up Manager
Wilmington, DE · On-site
Study Start Up Manager - Hybrid Role On-Site Are you ready to take on a pivotal role in the Site Activation Team as a Study Start Up Manager? As a key player in the US study team, you'll be ...
Study Start Up Coordinator's Main Objective Overall, the Study Start Up Coordinator is responsible for supporting efficient, accurate, and organized study start-up operations for clinical trials ...
Study Start Up Coordinator's Main Objective Overall, the Study Start Up Coordinator is responsible for supporting efficient, accurate, and organized study start-up operations for clinical trials ...
Study Start Up Manager
Wilmington, DE · Hybrid
Study Start Up Manager - Hybrid Role On-Site Are you ready to take on a pivotal role in the Site Activation Team as a Study Start Up Manager? As a key player in the US study team, you'll be ...
Study Start Up Manager
Wilmington, DE · Hybrid
Study Start Up Manager - Hybrid Role On-Site Are you ready to take on a pivotal role in the Site Activation Team as a Study Start Up Manager? As a key player in the US study team, you'll be ...
The Associate Director, Study Start Up & Records Management will interface with Site Directors and the study team to support operational aspects of study start-up and execution. Primary ...
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The Associate Director, Study Start Up & Records Management will interface with Site Directors and the study team to support operational aspects of study start-up and execution. Primary ...
Summary The Study Start-Up Manager (SSUM) reports to the Study Start-Up Team Lead and Study Start-Up Country Head and is accountable for endtoend study planning, study startup activities, and site ...
Summary The Study Start-Up Manager (SSUM) reports to the Study Start-Up Team Lead and Study Start-Up Country Head and is accountable for endtoend study planning, study startup activities, and site ...
Band Level 4 Summary The Study Start-Up Manager (SSUM) reports to the Study Start-Up Team Lead and Study Start-Up Country Head and is accountable for endtoend study planning, study startup activities ...
Band Level 4 Summary The Study Start-Up Manager (SSUM) reports to the Study Start-Up Team Lead and Study Start-Up Country Head and is accountable for endtoend study planning, study startup activities ...
Study Start Up Lead
South San Francisco, CA · On-site
As a member of the PDG Country Study Start-Up Team, your primary focus is to drive and facilitate efficient study start-up processes to contribute to the delivery of clinical trials to patients. You ...
Study Start Up Lead
South San Francisco, CA · On-site
As a member of the PDG Country Study Start-Up Team, your primary focus is to drive and facilitate efficient study start-up processes to contribute to the delivery of clinical trials to patients. You ...
Collaborate with Clinical Research Associates (CRAs) and the local study team to meet start-up milestones. * Participate in Local Study Team meetings and report on site performance metrics. * Ensure ...
Collaborate with Clinical Research Associates (CRAs) and the local study team to meet start-up milestones. * Participate in Local Study Team meetings and report on site performance metrics. * Ensure ...
Maintain timelines for study start-up through both internal and external collaboration; * Provide ... associates, as well as those that are new to the industry. The SAM Training Program embraces ...
Maintain timelines for study start-up through both internal and external collaboration; * Provide ... associates, as well as those that are new to the industry. The SAM Training Program embraces ...
Manager of Study Start Up
Blue Bell, PA · On-site
Manager of Study Start Up ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and ...
Manager of Study Start Up
Blue Bell, PA · On-site
Manager of Study Start Up ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and ...
Maintain timelines for study start-up through both internal and external collaboration; * Provide ... associates, as well as those that are new to the industry. The SAM Training Program embraces ...
Maintain timelines for study start-up through both internal and external collaboration; * Provide ... associates, as well as those that are new to the industry. The SAM Training Program embraces ...
Collaborate with Clinical Research Associates (CRAs) and the local study team to meet start-up milestones. Participate in Local Study Team meetings and report on site performance metrics. Ensure the ...
Collaborate with Clinical Research Associates (CRAs) and the local study team to meet start-up milestones. Participate in Local Study Team meetings and report on site performance metrics. Ensure the ...
Manager of Study Start Up
Blue Bell, PA · On-site +1
Manager of Study Start Up ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and ...
Manager of Study Start Up
Blue Bell, PA · On-site +1
Manager of Study Start Up ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and ...
... associates, as well as those that are new to the industry. The SAM Training Program embraces ... study start-up to advance clinical trials. Qualifications * A minimum of a PhD is required ...
... associates, as well as those that are new to the industry. The SAM Training Program embraces ... study start-up to advance clinical trials. Qualifications * A minimum of a PhD is required ...
Study Start Up Associate information
See salary details
$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
How much do study start up associate jobs pay per hour?
As of May 28, 2026, the average hourly pay for study start up associate in the United States is $31.54, according to ZipRecruiter salary data. Most workers in this role earn between $21.15 and $41.59 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.
More about Study Start Up Associate jobs
What cities are hiring for Study Start Up Associate jobs? Cities with the most Study Start Up Associate job openings:
What states have the most Study Start Up Associate jobs? States with the most job openings for Study Start Up Associate jobs include:
What job categories do people searching Study Start Up Associate jobs look for? The top searched job categories for Study Start Up Associate jobs are:
Job description
Summary
Qualifications
We are looking for a Study Start-Up Manager with extensive experience to lead clinical study start-up activities. This role requires a strong background in regulatory processes, site management, and expertise in ensuring compliance with local and international guidelines, particularly ICH-GCP.
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- Lead and manage start-up activities for clinical studies, ensuring compliance with local and international guidelines (ICH-GCP).
- Prepare, review, and track site regulatory documentation throughout the study start-up phase.
- Collaborate with Clinical Research Associates (CRAs) and the local study team to meet start-up milestones.
- Participate in Local Study Team meetings and report on site performance metrics.
- Ensure the timely submission of documents to regulatory authorities and maintain the trial master file (eTMF).
Qualifications
- Minimum 3 years of experience in Clinical Study Start-Up (full-time).
- At least 1 year of hands-on experience with Veeva Vault.
- Strong background in informed consent review and negotiation.
- Bachelor’s degree (higher degree preferred) with knowledge of clinical trial processes (Phases II-IV) and ICH-GCP.
- Excellent communication, organizational, and project management skills.
- Strong problem-solving and negotiation abilities.
About Cedent
Sourced by ZipRecruiter
CEDENT strives to attract and retain the best people and provide an environment where they can all develop professionally and build a rewarding career. As a result, we create an inclusive environment that is rich in diversity, acknowledges each individual's uniqueness and promotes respect, personal achievement and stewardship. Our clients are global and so is CEDENT. We build and maintain a global workforce that includes people from different backgrounds, with a vast range of skills and experience all united by a common culture and commitment to help our clients achieve high performance. Cultivating a diverse workforce and inclusive work environment makes business sense. Our peoples varied skills are the talent engine that powers CEDENT, enabling it in turn to deliver the innovative solutions that help our clients outperform competitors.
Industry
It services
Company size
11 - 50 Employees
Headquarters location
Plano, TX, US
Year founded
2008