Senior Software Developer
$53.75 - $70.75/hr
Suvoda is a global clinical trial technology company shaping digital experiences that enable ... As a Software Developer on Suvoda's Product team, you'll design and build clinical trial software ...
$53.75 - $70.75/hr
Suvoda is a global clinical trial technology company shaping digital experiences that enable ... As a Software Developer on Suvoda's Product team, you'll design and build clinical trial software ...
$53.75 - $70.75/hr
Suvoda is a global clinical trial technology company shaping digital experiences that enable ... As a Software Developer on Suvoda's Product team, you'll design and build clinical trial software ...
San Antonio, TX · On-site
$28.75 - $39.25/hr
Job Title: Clinical Trial Associate Reports To: PM Manager Department: Operations FLSA Status ... software. Work Environment and Physical Demands: The work environment and physical demands ...
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San Antonio, TX · On-site
$28.75 - $39.25/hr
Job Title: Clinical Trial Associate Reports To: PM Manager Department: Operations FLSA Status ... software. Work Environment and Physical Demands: The work environment and physical demands ...
New
Conshohocken, PA · On-site +1
$53.75 - $70.75/hr
Suvoda is a global clinical trial technology company shaping digital experiences that enable ... As a Software Developer on Suvoda's Product team, you'll design and build clinical trial software ...
Conshohocken, PA · On-site +1
$53.75 - $70.75/hr
Suvoda is a global clinical trial technology company shaping digital experiences that enable ... As a Software Developer on Suvoda's Product team, you'll design and build clinical trial software ...
Clinical Trial Manager (CTM) Location: Hampton, NJ Duration: 6 Months (Possible extension) SUMMARY ... Proficient computer skills with Microsoft Office software (Word, Excel, Project, PowerPoint and ...
Clinical Trial Manager (CTM) Location: Hampton, NJ Duration: 6 Months (Possible extension) SUMMARY ... Proficient computer skills with Microsoft Office software (Word, Excel, Project, PowerPoint and ...
Minnetonka, MN · On-site
Our medical devices, software and related services are used worldwide to diagnose and treat ... The position supports the execution of clinical studies by maintaining trial documentation ...
Minnetonka, MN · On-site
Our medical devices, software and related services are used worldwide to diagnose and treat ... The position supports the execution of clinical studies by maintaining trial documentation ...
Minnetonka, MN · On-site
Our medical devices, software and related services are used worldwide to diagnose and treat ... The position supports the execution of clinical studies by maintaining trial documentation ...
Minnetonka, MN · On-site
Our medical devices, software and related services are used worldwide to diagnose and treat ... The position supports the execution of clinical studies by maintaining trial documentation ...
Malvern, PA · On-site
... trial execution ensuring prompt resolution and compliance with all SOP, GMP, Quality, and ... Clinical Supply Distribution Clinical Study Execution/GCP Intermediate to advanced software skills ...
Malvern, PA · On-site
... trial execution ensuring prompt resolution and compliance with all SOP, GMP, Quality, and ... Clinical Supply Distribution Clinical Study Execution/GCP Intermediate to advanced software skills ...
Houston, TX · On-site
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. * Excellent communication, interpersonal, and stakeholder ...
Houston, TX · On-site
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. * Excellent communication, interpersonal, and stakeholder ...
Dallas, TX · On-site
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. * Excellent communication, interpersonal, and stakeholder ...
Dallas, TX · On-site
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. * Excellent communication, interpersonal, and stakeholder ...
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. * Excellent communication, interpersonal, and stakeholder ...
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. * Excellent communication, interpersonal, and stakeholder ...
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. * Excellent communication, interpersonal, and stakeholder ...
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. * Excellent communication, interpersonal, and stakeholder ...
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. * Excellent communication, interpersonal, and stakeholder ...
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. * Excellent communication, interpersonal, and stakeholder ...
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. * Excellent communication, interpersonal, and stakeholder ...
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. * Excellent communication, interpersonal, and stakeholder ...
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. * Excellent communication, interpersonal, and stakeholder ...
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. * Excellent communication, interpersonal, and stakeholder ...
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. * Excellent communication, interpersonal, and stakeholder ...
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. * Excellent communication, interpersonal, and stakeholder ...
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. * Excellent communication, interpersonal, and stakeholder ...
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. * Excellent communication, interpersonal, and stakeholder ...
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. * Excellent communication, interpersonal, and stakeholder ...
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. * Excellent communication, interpersonal, and stakeholder ...
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. * Excellent communication, interpersonal, and stakeholder ...
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. * Excellent communication, interpersonal, and stakeholder ...
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. * Excellent communication, interpersonal, and stakeholder ...
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. * Excellent communication, interpersonal, and stakeholder ...
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. * Excellent communication, interpersonal, and stakeholder ...
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. * Excellent communication, interpersonal, and stakeholder ...
$11.54 - $16.74
4% of jobs
$16.74 - $21.94
15% of jobs
$24.54 is the 25th percentile. Wages below this are outliers.
$21.94 - $27.14
13% of jobs
$27.14 - $32.34
8% of jobs
The median wage is $35.23 / hr.
$32.34 - $37.54
19% of jobs
$37.54 - $42.74
13% of jobs
$44.83 is the 75th percentile. Wages above this are outliers.
$42.74 - $47.95
10% of jobs
$47.95 - $53.15
5% of jobs
$53.15 - $58.35
11% of jobs
$58.35 - $63.55
1% of jobs
$63.55 - $68.75
1% of jobs
$11
$37
$68
| Aspect | Clinical Trial Software | Clinical Research Coordinator |
|---|---|---|
| Primary Role | Software tools used to manage, track, and analyze clinical trial data | Manages daily activities of clinical trials, including patient recruitment and data collection |
| Required Skills | Technical knowledge of software systems, data management, and compliance | Clinical knowledge, organization, communication, and regulatory understanding |
| Work Environment | Technology-focused, often in office or remote settings | Hospital, clinic, or research facility |
| Industry Usage | Used by clinical trial teams, data managers, and IT professionals | Employed directly by research institutions, hospitals, or pharmaceutical companies |
While Clinical Trial Software involves the tools used to facilitate and manage clinical trials, Clinical Research Coordinators are the professionals who execute and oversee the trial processes. Both roles are essential in the clinical research industry but serve different functions—one focuses on software solutions, the other on trial management and coordination.

About Suvoda:
Suvoda is a global clinical trial technology company shaping digital experiences that enable clinical trial sponsor and site professionals to take full command over the inherent logistical complexity behind mission-critical and time-sensitive patient interactions in life-sustaining studies for therapeutic areas such as oncology, central nervous system, and rare disease. Headquartered in the greater Philadelphia area, with offices in Bucharest and Iasi, Barcelona, Portland, OR, and Tokyo, JP, we've experienced impressive year-over-year growth and are growing our teams across the globe. Learn more about us on our website!
As a Software Developer on Suvoda's Product team, you'll design and build clinical trial software that directly supports mission-critical, time-sensitive patient interactions in life-sustaining studies across oncology, CNS, and rare disease. You'll work in agile, cross-functional teams to deliver high-quality features and services, with a relentless focus on patient safety and the integrity of clinical study data. Here, your code doesn't just ship product-it helps sponsors, sites, and patients navigate some of the most complex, high-stakes trials in the world, while you grow your craft alongside experienced engineers in a modern, continuously improving SDLC.
Responsibilities:Â
Requirements:
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Pharmaceutical and medicine manufacturing
1,001 - 5,000 Employees
Conshohocken, PA, US
2012