The Study Management group serves as the operational backbone of clinical trial delivery, owning the full lifecycle of assigned studies from onboarding through closeout. The Associate Global Study ...
The Study Management group serves as the operational backbone of clinical trial delivery, owning the full lifecycle of assigned studies from onboarding through closeout. The Associate Global Study ...
Director, Regional Clinical Study Management
$171K - $231K/yr
Provides leadership, management, and/or mentorship to associate directors, clinical study managers at various levels for assigned portfolio * Collaborates effectively with internal and external ...
Director, Regional Clinical Study Management
$171K - $231K/yr
Provides leadership, management, and/or mentorship to associate directors, clinical study managers at various levels for assigned portfolio * Collaborates effectively with internal and external ...
Specialist Study Management
Wilmington, DE · On-site
Excellent employment opportunity for a Specialist Study Management in the Wilmington, DE area. Candidates must be local to Wilmington, DE, non-remote position * Own and maintain quality for the study ...
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Specialist Study Management
Wilmington, DE · On-site
Excellent employment opportunity for a Specialist Study Management in the Wilmington, DE area. Candidates must be local to Wilmington, DE, non-remote position * Own and maintain quality for the study ...
The Study Management group serves as the operational backbone of clinical trial delivery, owning the full lifecycle of assigned studies from onboarding through closeout. The Associate Global Study ...
The Study Management group serves as the operational backbone of clinical trial delivery, owning the full lifecycle of assigned studies from onboarding through closeout. The Associate Global Study ...
Clinical Trial Management Associate
Boston, MA · On-site +1
$36.50 - $49.75/hr
The Clinical Trial Management Associate (CTMA) works as part of the Study Management Team to ... Conducts study tracking (e.g., CTMS, start-up, milestone, close-out); generates, reviews and ...
Clinical Trial Management Associate
Boston, MA · On-site +1
$36.50 - $49.75/hr
The Clinical Trial Management Associate (CTMA) works as part of the Study Management Team to ... Conducts study tracking (e.g., CTMS, start-up, milestone, close-out); generates, reviews and ...
Clinical Trial Management Associate
Carlsbad, CA · On-site +1
$34.50 - $47.25/hr
The Clinical Trial Management Associate (CTMA) works as part of the Study Management Team to ... Conducts study tracking (e.g., CTMS, start-up, milestone, close-out); generates, reviews and ...
Clinical Trial Management Associate
Carlsbad, CA · On-site +1
$34.50 - $47.25/hr
The Clinical Trial Management Associate (CTMA) works as part of the Study Management Team to ... Conducts study tracking (e.g., CTMS, start-up, milestone, close-out); generates, reviews and ...
Clinical Trial Management Associate
Carlsbad, CA · On-site +1
$34.50 - $47.25/hr
The Clinical Trial Management Associate (CTMA) works as part of the Study Management Team to ... Conducts study tracking (e.g., CTMS, start-up, milestone, close-out); generates, reviews and ...
Clinical Trial Management Associate
Carlsbad, CA · On-site +1
$34.50 - $47.25/hr
The Clinical Trial Management Associate (CTMA) works as part of the Study Management Team to ... Conducts study tracking (e.g., CTMS, start-up, milestone, close-out); generates, reviews and ...
Position The Associate Director, Clinical Study Management, EMEA/LATAM will be responsible for overseeing the execution of clinical trials in oncology and other therapeutic areas, as required. This ...
Position The Associate Director, Clinical Study Management, EMEA/LATAM will be responsible for overseeing the execution of clinical trials in oncology and other therapeutic areas, as required. This ...
Position As a Clinical Trial Management Associate (CTMA), you will serve as a critical inhouse ... You will independently manage assigned study responsibilities and help ensure the delivery of high ...
Position As a Clinical Trial Management Associate (CTMA), you will serve as a critical inhouse ... You will independently manage assigned study responsibilities and help ensure the delivery of high ...
Clinical Trial Management Associate, Oncology (EMEA/LATAM)
Millbrae, CA · On-site
$39 - $53/hr
Position As a Clinical Trial Management Associate (CTMA), you will serve as a critical inhouse ... You will independently manage assigned study responsibilities and help ensure the delivery of high ...
Clinical Trial Management Associate, Oncology (EMEA/LATAM)
Millbrae, CA · On-site
$39 - $53/hr
Position As a Clinical Trial Management Associate (CTMA), you will serve as a critical inhouse ... You will independently manage assigned study responsibilities and help ensure the delivery of high ...
Position The Associate Director, Clinical Study Management, EMEA/LATAM will be responsible for overseeing the execution of clinical trials in oncology and other therapeutic areas, as required. This ...
Position The Associate Director, Clinical Study Management, EMEA/LATAM will be responsible for overseeing the execution of clinical trials in oncology and other therapeutic areas, as required. This ...
Global Case Management Associate
Danbury, CT · On-site
... Studies, License Partner's information and Product Complaints, documenting the results ... The global Case Management Associate in PSPV supports the reconciliation process for these sources ...
Global Case Management Associate
Danbury, CT · On-site
... Studies, License Partner's information and Product Complaints, documenting the results ... The global Case Management Associate in PSPV supports the reconciliation process for these sources ...
Senior Clinical Trials Management Associate
Parsippany, NJ · On-site
$115K - $149K/yr
The Senior Clinical Trials Management Associate is a primarily an in-house sponsor position ... Prepares and/or reviews study-related or essential study start-up documents as they relate to the ...
Senior Clinical Trials Management Associate
Parsippany, NJ · On-site
$115K - $149K/yr
The Senior Clinical Trials Management Associate is a primarily an in-house sponsor position ... Prepares and/or reviews study-related or essential study start-up documents as they relate to the ...
Senior Clinical Trials Management Associate
Santa Monica, CA · On-site
$115K - $149K/yr
The Senior Clinical Trials Management Associate is a primarily an in-house sponsor position ... Prepares and/or reviews study-related or essential study start-up documents as they relate to the ...
Senior Clinical Trials Management Associate
Santa Monica, CA · On-site
$115K - $149K/yr
The Senior Clinical Trials Management Associate is a primarily an in-house sponsor position ... Prepares and/or reviews study-related or essential study start-up documents as they relate to the ...
Senior Clinical Trials Management Associate
El Segundo, CA · On-site
$115K - $149K/yr
The Senior Clinical Trials Management Associate is a primarily an in-house sponsor position ... Prepares and/or reviews study-related or essential study start-up documents as they relate to the ...
Senior Clinical Trials Management Associate
El Segundo, CA · On-site
$115K - $149K/yr
The Senior Clinical Trials Management Associate is a primarily an in-house sponsor position ... Prepares and/or reviews study-related or essential study start-up documents as they relate to the ...
Senior Clinical Trials Management Associate
$115K - $149K/yr
The Senior Clinical Trials Management Associate is a primarily an in-house sponsor position ... Prepares and/or reviews study-related or essential study start-up documents as they relate to the ...
Senior Clinical Trials Management Associate
$115K - $149K/yr
The Senior Clinical Trials Management Associate is a primarily an in-house sponsor position ... Prepares and/or reviews study-related or essential study start-up documents as they relate to the ...
Senior Clinical Trials Management Associate
Foster City, CA · On-site
$115K - $149K/yr
The Senior Clinical Trials Management Associate is a primarily an in-house sponsor position ... Prepares and/or reviews study-related or essential study start-up documents as they relate to the ...
Senior Clinical Trials Management Associate
Foster City, CA · On-site
$115K - $149K/yr
The Senior Clinical Trials Management Associate is a primarily an in-house sponsor position ... Prepares and/or reviews study-related or essential study start-up documents as they relate to the ...
Senior Clinical Trials Management Associate
Santa Monica, CA · On-site
$115K - $149K/yr
The Senior Clinical Trials Management Associate is a primarily an in-house sponsor position ... Prepares and/or reviews study-related or essential study start-up documents as they relate to the ...
Senior Clinical Trials Management Associate
Santa Monica, CA · On-site
$115K - $149K/yr
The Senior Clinical Trials Management Associate is a primarily an in-house sponsor position ... Prepares and/or reviews study-related or essential study start-up documents as they relate to the ...
Senior Clinical Trials Management Associate
$115K - $149K/yr
The Senior Clinical Trials Management Associate is a primarily an in-house sponsor position ... Prepares and/or reviews study-related or essential study start-up documents as they relate to the ...
Senior Clinical Trials Management Associate
$115K - $149K/yr
The Senior Clinical Trials Management Associate is a primarily an in-house sponsor position ... Prepares and/or reviews study-related or essential study start-up documents as they relate to the ...
Senior Clinical Trials Management Associate
$115K - $149K/yr
The Senior Clinical Trials Management Associate is a primarily an in-house sponsor position ... Prepares and/or reviews study-related or essential study start-up documents as they relate to the ...
Senior Clinical Trials Management Associate
$115K - $149K/yr
The Senior Clinical Trials Management Associate is a primarily an in-house sponsor position ... Prepares and/or reviews study-related or essential study start-up documents as they relate to the ...
Study Management Associate information
What are the key skills and qualifications needed to thrive as a Study Management Associate, and why are they important?
What is the difference between Study Management Associate vs Clinical Research Coordinator?
| Aspect | Study Management Associate | Clinical Research Coordinator |
|---|---|---|
| Required Credentials | Bachelor's degree, relevant certifications often preferred | Bachelor's degree, often with certifications like CCRP |
| Work Environment | Pharmaceutical companies, CROs, research institutions | Hospitals, clinics, research sites |
| Employer & Industry Usage | Used in industry-sponsored trials and clinical research firms | Common in academic and hospital-based studies |
| Search & Comparison Intent | High overlap in job duties and qualifications | Similar roles with some operational differences |
The Study Management Associate and Clinical Research Coordinator roles share many similarities, including required education and work environments. However, the Study Management Associate typically focuses on supporting study operations within industry settings, while the Clinical Research Coordinator often manages patient interactions and site activities in clinical settings. Both roles are essential in advancing clinical research but differ slightly in scope and daily responsibilities.
What are the typical responsibilities of a Study Management Associate in a clinical research team?
What is a Study Management Associate?
- Associate Director Clinical Data Management
- Associate Director Clinical Operations
- Associate Director Clinical Research
- Irb Director
- Biotech Startup Director Clinical Operations
- Contract Apple Clinical Research
- Gcps
- Global Clinical Trial Manager
- Associate Clinical Data Manager
- Manager Pfizer Clinical Research

Job description
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.
Supporting clinical trials means supporting unique experiments that are inherently complex, high-stakes, and dynamic. It is imperative that Suvoda staff working with clients, end-users, or the systems that client and end-users interact with understand the clinical trial industry, regulations, Suvoda's software products and processes, and especially the specificities of the unique trial in question before taking any actions they may alter the data of the system in question.
The Concierge team operates at the intersection of clinical trial operations and participant support, delivering travel and payment services across both the Concierge and Site Driven delivery models. The Study Management group serves as the operational backbone of clinical trial delivery, owning the full lifecycle of assigned studies from onboarding through closeout.Â
The Associate Global Study Manager balances administrative coordination with hands-on, customer-facing study support, acting as an extension of the Global Study Manager in maintaining accurate records, resolving day-to-day requests, and helping ensure studies stay compliant and on track.
Responsibilities:
Administrative Responsibilities
- Route incoming correspondence to the appropriate team member for action;
- Audit study documentation and shared files for accuracy and adherence to internal procedures;
- Prepare recurring internal and customer-facing reports;
- Assist in the maintenance of internally stored data;
- Support additional administrative and operational needs as assigned, which may include tracking participant transfers between studies, preparing expense-tracking materials, and coordinating region-specific documentation requirements;
Operational & Customer-Facing Responsibilities
- Create and maintain study playbooks that internal stakeholders use to stay aligned on study details, requirements, and expectations;
- Monitor and help resolve customer- and site-submitted requests for exceptions to standard study terms, escalating to the Global Study Manager as needed;
- Review coordinator-submitted activity on a recurring basis to catch and resolve discrepancies;
- Audit participant consent documentation on a quarterly basis;
- Monitor a shared safety-alert channel for events that could affect participant travel, escalating urgent matters promptly to the appropriate study team members;
- Serve as the customer-facing point of contact for a subset of studies requiring dedicated regional support, including coordinator onboarding and exception management for those studies;
- Act as a secondary point of contact after Global Study Manager for customer inquiries and day-to-day relationship management;
Qualifications:
- Bachelor's degree in Business, Healthcare Administration, Health Policy, or a related field preferred; equivalent experience considered;
- 1-3 years of post-graduate experience, including internships or entry-level project or study coordination work;
- Proficiency with common business and reporting software; ability to quickly learn internal systems and platforms;
- Strong written and oral communication skills, with good judgment about when and how to escalate customer- or participant-facing issues;
- High attention to detail, especially when auditing data or documentation for accuracy;
- Strong organizational skills; able to manage multiple recurring tasks and deadlines across a portfolio of studies;
- Discretion in handling sensitive information;
- Capable of working independently following training, with clearly defined escalation path to senior study management position;
- Comfortable operating across a range of digital tools - including Microsoft 365 and emerging AI-assisted technologies - with the adaptability to pick up new systems quickly;
- Strong interpersonal instincts - able to build trust with customers and participants alike, and to bring a human touch to what is often a sensitive, high-stakes experience.
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About Suvoda
Sourced by ZipRecruiter
Industry
Pharmaceutical and medicine manufacturing
Company size
1,001 - 5,000 Employees
Headquarters location
Conshohocken, PA, US
Year founded
2012